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Cell Stem Cell. Author manuscript; available in PMC 2017 May 05. Published in final edited form as: Cell Stem Cell. 2016 May 5; 18(5): 668–681. doi:10.1016/j.stem.2016.03.002.
TGF-β Inhibition Rescues Hematopoietic Stem Cell Defects and Bone Marrow Failure in Fanconi Anemia Haojian Zhang1, David E Kozono1, Kevin W O’Connor1, Sofia Vidal-Cardenas1, Alix Rousseau2, Abigail Hamilton1, Lisa Moreau1, Emily F Gaudiano1, Joel Greenberger3, Grover Bagby4, Jean Soulier2, Markus Grompe4, Kalindi Parmar1, and Alan D D’Andrea1 1Department
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2Institute
of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA
of hematology (IUH), University Paris-Diderot, Sorbonne Paris Cite 75010
3Department
of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA
15213, USA 4Oregon
Health and Science University, Portland, OR 97239, USA
SUMMARY
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Fanconi Anemia (FA) is an inherited DNA repair disorder characterized by progressive bone marrow failure (BMF) from hematopoietic stem and progenitor cell (HSPC) attrition. A greater understanding of the pathogenesis of BMF could improve the therapeutic options for FA patients. Using a genome-wide shRNA screen in human FA fibroblasts, we identify transforming growth factor-β (TGF-β) pathway-mediated growth suppression as a cause of BMF in FA. Blocking the TGF-β pathway improves the survival of FA cells and rescues the proliferative and functional defects of HSPCs derived from FA mice and FA patients. Inhibition of TGF-β signaling in FA HSPCs results in elevated homologous recombination (HR) repair with a concomitant decrease in non-homologous end-joining (NHEJ), accounting for the improvement in cellular growth. Together, our results suggest that elevated TGF-β signaling contributes to the BMF in FA by impairing HSPC function, and may be a potential therapeutic target for the treatment of FA.
INTRODUCTION Hematopoietic stem cells (HSCs) replenish the blood system throughout the life span of an organism and maintain homeostasis. Consequently, depletion or impairment of the HSC
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Corresponding Author: Alan D. D’Andrea, M.D., Director: Center for DNA Damage and Repair, The Fuller-American Cancer Society Professor, Harvard Medical School, Chief, Division of Genomic Stability and DNA Repair, Department of Radiation Oncology and Pediatrics, Dana-Farber Cancer Institute, Mayer 640, 450 Brookline Ave., Boston, MA 02215, 617-632-2080, FAX: 617-632-5757, [email protected]. AUTHOR CONTRIBUTIONS H.Z. and A.D.D designed experiments. H.Z., D.E.K., K.W.O., S.V., A.R., A.H., L.M., E.F.G., and K.P., performed experiments with help from J.G., G.B., J.S., and M.G.. H.Z., D.E.K., K.P., and A.D.D. analyzed and interpreted the data. H.Z., K.P., and A.D.D. wrote the manuscript. Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
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reservoir leads to hematopoietic failure or hematologic malignancies. Accumulation of DNA damage and genomic instability, due to physiological stress or exposure to genotoxic agents, is one of the mechanisms of loss of HSC reserve (Garaycoechea et al., 2012; Mandal et al., 2011; Walter et al., 2015). Protective cellular DNA repair mechanisms exist in HSCs to combat the accumulation of DNA damage. Accordingly, the genetic ablation of proteins (e.g. Atm, Lig4, ATR) involved in DNA repair pathways in mice results in severe HSC defects (Ito et al., 2006; Niedernhofer, 2008; Rossi et al., 2007; Ruzankina et al., 2007), and the NHEJ pathway is the most commonly used DNA repair mechanism in quiescent HSCs (Milyavsky et al., 2010; Mohrin et al., 2010).
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Fanconi anemia (FA) is the most common inherited bone marrow failure (BMF) syndrome. FA patients develop progressive bone marrow failure during childhood. In addition, FA patients also develop other hematologic manifestations, including myelodisplastic syndrome (MDS) and acute myeloid leukemia (AML) due to clonal evolution (Shimamura and Alter, 2010). Current therapies for hematologic manifestations in FA include hematopoietic stem cell transplant and treatment with growth factors and androgens. While an allogenic bone marrow transplant from a histocompatible sibling donor remains the optimal long-term therapy, many FA patients do not have a suitable donor. Moreover, transplant may contribute to increased incidence of later, non-hematologic consequence such as secondary solid tumors and endocrine failure (Shimamura and Alter, 2010). Therefore, novel alternative treatment options to treat marrow failure in FA patients are needed.
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FA is caused by biallelic mutation in one of eighteen FANC genes (FANC-A, B, C, D1, D2, E, F, G, I, J, L, M, N, O, P, Q, S, T), the products of which cooperate in the FA/BRCA DNA repair pathway and regulate cellular resistance to DNA cross-linking agents (Kottemann and Smogorzewska, 2013; Sawyer et al., 2015). Due to the underlying DNA repair defect, FA cells are hypersensitive to genotoxic DNA crosslinking agents. Although the precise biochemical functions of the FA/BRCA pathway in DNA repair remain unclear, the pathway promotes homologous recombination (HR) repair (Deans and West, 2011). The FA/BRCA pathway also regulates cytokinesis, and pathway disruption results in increased binucleate bone marrow cells and apoptosis (Chan et al., 2009; Naim and Rosselli, 2009; Vinciguerra et al., 2010). FA cells are also uniquely hypersensitive to oxidative stress and apoptotic cytokines, such as IFNγ and TNFα (Pang and Andreassen, 2009).
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All blood lineages are deficient in FA patients (Butturini et al., 1994), suggesting that the FA pathway regulates the function of hematopoietic stem and progenitor cells (HSPCs). Accordingly, recent studies indicate that the BMF in FA is attributable to an impaired HSPC pool. HSPCs in FA patients and FA mice exhibit reduced cell number and compromised stem cell function (Ceccaldi et al., 2012; Crossan et al., 2011; Parmar et al., 2009; Parmar et al., 2010; Zhang et al., 2010). The primary mechanism of the impairment of HSPCs leading to the BMF in FA, however, remains elusive. Due to the well-defined role of the FA/BRCA pathway in repairing DNA damage (Deans and West, 2011; Kottemann and Smogorzewska, 2013), DNA damage accumulation in HSPCs may be one of the major causes for BMF in FA. Indeed, recent studies suggest that BMF in FA and impaired HSPC function result from the genotoxicity of endogenous crosslinking agents or from physiological stress (Garaycoechea et al., 2012; Langevin et al., 2011; Walter et al., 2015). Bone marrow failure
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in FA may also result, directly or indirectly, from hyperactivation of cell autonomous or microenvironmental growth suppressive pathways, induced in part, due to genotoxic stress. We have recently shown that one suppressive mechanism results from a hyperactive p53 response in HSPCs from FA patients (Ceccaldi et al., 2012). Here, we performed an unbiased shRNA screen to identify additional growth suppressive pathways which may account for the impairment/attrition of the FA bone marrow HSPCs. We identified hyperactive TGF-β signaling in HSPCs as a mechanism of bone marrow suppression in FA. Disruption of TGF-β signaling significantly protected HSCs in FA from genotoxic stress by increasing HR activity and decreasing NHEJ activity.
RESULTS TGF-β Pathway Blocks FA Cell Survival in the Presence of Genotoxic Agents
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We initially performed a genome-wide shRNA screen in a patient-derived FANCA−/− fibroblast line in order to identify genes whose knockdown can rescue the FA phenotype in the presence of a genotoxic agent, Mitomycin C (MMC) (Figure S1A and S1B). Multiple TGF-β pathway genes (e.g. SMAD3, BMP2, PDCD4) were among the top hits (Figure 1A). shRNAs targeted against NQO1 and NFE2L2 genes involved in MMC metabolism (Siegel et al., 2012) also scored positive (Figure 1A), validating our screen for MMC resistance. The TGF-β pathway is known to contribute to hematopoietic suppression in other human diseases, such as myelodysplastic syndrome (MDS) (Suragani et al., 2014; Zhou et al., 2011; Zingariello et al., 2013), suggesting a more general mechanism in BMF. We next validated our primary screening data in a number of FA cell lines. The respective cell lines, which were corrected by reconstitution with FANCA or FANCG cDNAs, were used as positive controls as they were more resistant to MMC compared to the uncorrected FA cells (Figure 1B–1D). Both knockdown of SMAD3 and pharmacologic inhibition of the TGF-β pathway with small molecules, SD208 and SIS3, significantly enhanced the survival of FA cells in the presence of MMC (Figure 1B–1D, and S1C).
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DNA damage caused by an endogenous genotoxic agent, acetaldehyde, requires the FA pathway for repair (Garaycoechea et al., 2012). Accordingly, we identified an FA patientderived FANCG-deficient lymphoblast line, EUFA316, which is hypersensitive to acetaldehyde (Figure S1D). Both pharmacologic inhibition by SD208 and genetic depletion by shRNA of the TGF-β pathway promoted cellular survival in the presence of acetaldehyde (Figure 1E and 1F). Additionally, disruption of the TGF-β pathway by shRNA or by SD208 resulted in reduced p53 and p21 protein levels (Figure S1E). Together, these data demonstrate that targeting the TGF-β pathway can reduce the genotoxic stress mediated growth inhibition of human FA cells. TGF-β Pathway Inhibition Rescues the Functional Defects of HSCs from FA Mice As FA mice exhibit HSPC defects, the possible suppressive function of the TGF-β pathway in bone marrow HSPCs of FA mice was next examined. Elevated expression levels of both Tgfb1 and Smad3 were observed in Fancd2−/− HSPCs [Lin−Sca-1+c-Kit+ (LSK) population] (Figure 2A). Elevated pSmad2/3 protein levels were also observed in Fancd2−/− HSPCs (Figure S2A and S2B). Moreover, enhanced mRNA expression of TGF-β pathway target
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genes, including Cdkn1a, Cdkn1c, Foxp3, and Atg5, was also observed in Fancd2−/− HSPCs (Figure 2A), implying that the TGF-β pathway is upregulated in FA HSPCs. Fancd2−/− bone marrow HSPCs were more sensitive to TGF-β1 than wild-type HSPCs (Figure S2C). Therefore, we hypothesized that inhibition of this pathway might rescue the defect of FA HSPCs. Colony forming assays showed that the clonogenic ability of Fancd2−/− HSPCs was inhibited by TGF-β1; blockade of the TGF-β signaling by 1D11 (a neutralizing antibody against mouse TGF-β) (Brenet et al., 2013) or SD208 markedly enhanced the clonogenic ability (Figure S2D–S2F). Further, genetic knockdown of Smad3 promoted the in vitro expansion of HSPCs and in vivo engraftment of Lin− cells from bone marrow of Fancd2−/− mice (Figure 2B, 2C, and S2G–S2J). Taken together, inhibition of the TGF-β pathway can rescue the functional defects of Fancd2−/− HSPCs.
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Hyperactive TGF-β pathway signaling in Fancd2−/− HSPCs prompted us to assess whether the FA pathway components directly transcriptionally regulate the expression of TGF-β pathway genes. We first confirmed that mutation in FA genes results in hyperactive TGF-β activity. We transfected a TGF-β luciferase reporter vector containing SMAD binding element, into FA cells or corrected FA cells. Interestingly, increased TGF-β luciferase activity was observed in FA-A cells compared to FANCA-corrected cells (Figure S2K). Conversely, overexpression of FANCD2 in 293T cells significantly reduced the TGF-β luciferase reporter activity (Figure 2D). Using chromatin immunoprecipitation (ChIP) assays, we previously showed that activated FANCD2 increases the transcriptional activity of the TAp63 gene (Park et al., 2013). A genome-wide ChIP sequencing (ChIP-seq) analysis, using FANCD2 antibody, demonstrated that FANCD2 also binds to SMAD gene promoters (Park et al., 2013). ChIP confirmed that FANCD2 can directly bind to the promoter region of a SMAD gene, suggesting that FANCD2 decreases the transcriptional activity of SMAD genes. Interestingly, FANCD2 bound to the promoter of SMAD1 in 293T cells (Figure 2E). The binding of FANCD2 to the promoter of SMAD1 was observed in corrected FA cells, but not in the parental FA cells (EUFA316 and GM6914), suggesting that a functional FA pathway is required for the FANCD2-mediated transcriptional decrease of the TGFβ pathway gene (Figure 2F and S2L). Collectively, these results demonstrate that disruption of the FA pathway causes transcriptional changes, resulting in hyperactive TGF-β signaling. TGF-β Pathway Inhibition Rescues Acetaldehyde-induced Genotoxicity in HSPCs from FA Mice
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DNA damage induced by the endogenous genotoxic agents, such as acetaldehyde, causes the attrition of HSCs, leading to spontaneous bone marrow failure in murine FA models (Garaycoechea et al., 2012; Langevin et al., 2011). We reasoned that blockade of the TGF-β pathway may contribute to the repair of acetaldehyde-induced DNA damage in FA HSCs. As expected, bone marrow cells from Fancd2−/− mice were sensitive to acetaldehyde exposure. The neutralizing anti-TGF-β antibody 1D11 treatment counteracted the genotoxic effects of acetaldehyde, and rescued the growth and clonogenic capacity of Fancd2−/− HSCs or Lin− cells from bone marrow (Figure 3A and S3A). To directly measure the protective effect of 1D11 on the survival of HSPCs after acetaldehyde exposure, a stem cell transplant was performed. The percentage of donor-derived cells at 4 and 16 weeks post transplantation was higher in recipients of 1D11 treated Fancd2−/− group than those in the isotype control group
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(Figure 3B and S3B), and 1D11 did not significantly affect the lineage differentiation of HSPCs (Figure S3C). Furthermore, γH2AX foci, a marker for DNA damage, resolved more rapidly in 1D11 treated Fancd2−/− cells, suggesting an improvement of DNA repair (Figure 3C, 3D, and S3D). Repair of DNA damage was further confirmed by comet assay (Figure 3E, 3F, and S3E). 1D11 treated Fancd2−/− cells also showed improvement in DNA repair when DNA damage was directly assessed by alkaline comet assay and confirmed that acetaldehyde-induced γH2AX foci indeed correspond to unrepaired double strand breaks (Figure 3E, 3F, and S3E), Taken together, pharmacologic inhibition of the TGF-β pathway by 1D11 promotes resistance of FA cells to endogenous genotoxic agents, and partially corrects the impaired stem cell function by promoting DNA repair. Inhibition of TGF-β Pathway Rescues Physiological Stress-induced Bone Marrow Failure in FA Mice
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Physiological stress-induced DNA damage is a source of DNA damage in HSCs in FA. The accumulation of physiological stress-induced DNA damage results in a collapse of the hematopoietic system in a murine FA model (Walter et al., 2015). Interestingly, polyinosinic:polycytidylic acid (pI:pC) exposure caused activation of TGF-β pathway in HSPCs (Figure S4A). To determine whether inhibition of TGF-β pathway also counteracts the genomic instability of HSCs caused by physiological stress, we simultaneously treated WT and Fancd2−/− mice for 48h with pI:pC (to induce stress) and 1D11 (to block the TGF-β pathway). As previously described (Walter et al., 2015), administration of pI:pC induced DNA damage in HSCs and caused increased levels of γH2AX and 53BP1 foci (Figure 4A– 4D and S4B); inhibition of the TGF-β pathway by 1D11 markedly reduced the pI:pCinduced DNA damage (Figure 4A–4D, S4B, and S4C). Importantly, inhibition of the TGF-β pathway rescued the viability of Fancd2−/− total bone marrow cells following pI:pC treatment (Figure S4D). Consistent with the previous study (Walter et al., 2015), pI:pC exposure induced oxidative stress in HSPCs from Fancd2−/− mice, however, 1D11 did not affect the level of oxidative stress (Figure S4E). As expected, pI:pC exposure induced proliferation of HSPCs, resulting in a concomitant reduction in the frequencies of quiescent cells. Interestingly, 1D11 treatment reduced pI:pC-induced cell cycling and increased the percentage of quiescent HSPCs, perhaps accounting for the improved DNA repair (Figure S4F). Thus, TGF-β pathway inhibition counteracts physiological stress-induced DNA damage in HSCs.
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To determine whether TGF-β pathway inhibition rescues pI:pC induced bone marrow failure, we treated WT and Fancd2−/− mice with pI:pC and 1D11 (Figure 4E). Interestingly, four weeks of pI:pC treatment caused peripheral blood pancytopenia in isotype control antibody-treated Fancd2−/− mice with reduction in red blood cells (RBC), white blood cells (WBC) and hemoglobin levels (Figure 4F). However, administration of 1D11 significantly prevented these peripheral blood abnormalities (Figure 4F). To examine the bone marrow HSC function, we next transplanted bone marrow cells from these pI:pC (plus or minus 1D11) treated donor mice into lethally irradiated recipients and evaluated spleen colonyforming units (CFU-S), thus allowing the quantification of the surviving multipotent shortterm HSCs. As expected, pI:pC treatment caused a marked reduction in the CFU-S content of Fancd2−/− bone marrow, and 1D11 improved this defect (Figure 4G). Consistent with
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these results, in a competitive repopulation experiment, recipient mice transplanted with bone marrow from 1D11 treated Fancd2-/- mice showed improved short-term donor cell engraftment compared to the recipients transplanted with isotype control (Figure 4H). Bone marrow HSPCs from Fancd2−/− mice treated with 1D11 also exhibited less DNA damage upon pI:pC exposure (Figure 4I, 4J, and S4G). Together, these data suggest that TGF-β pathway inhibition rescues pI:pC-induced bone marrow failure in FA mice and may be effective in preventing the bone marrow collapse of FA patients observed after viral infections. TGF-β Pathway Inhibition Restores the Function of HSPCs Derived from Humans with FA
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We next extended our studies in HSPCs derived from patients with FA. Primary human FA bone marrow cells demonstrated increased mRNA expression of multiple TGF-β pathway components (Figure 5A and S5A). TGF-β pathway inhibition, by knockdown of SMAD3 or by exposure to anti-human TGF-β neutralizing antibody GC1008, rescued the clonogenic defects of primary HSPCs from bone marrow of FA patients, although to a lesser extent than the rescue observed following p53 knockdown (Figure 5B–5F and S5B). Variable response to TGF-β pathway inhibition in primary human FA patient HSPCs may result from differences in the age, gender, intrinsic genetic differences, the levels of SMAD3/p53 in HSPCs, or the severity of the pre-existing bone marrow failure. Depletion of SMAD3 in FAlike primary HSPCs established by FANCD2 knockdown in human cord blood CD34+ cells, also rescued their clonogenicity, and partially restored MMC resistance (Figure 5G–5I and S5C). Inhibition of TGF-β signaling by GC1008 also recapitulated this phenotype by markedly rescuing the clonogenic capacity of FA-like HSPCs (Figure 5J and S5D). Further, since the very low CD34+ cell numbers in FA patients did not allow efficient xenograft assays for analysis of clonogenicity in vivo, we performed a surrogate in vivo xenograft assay using FA-like CD34+ cells. Strikingly, GC1008 treatment in vivo enhanced the engraftment of primary FA-like CD34+ cells (Figure 5K and S5E). In addition, we observed a higher frequency of FA-like HSPCs with γH2AX and 53BP1 foci upon MMC exposure, compared to the control HSPCs (Figure 5L, 5M, S5F and S5G). Exposure to GC1008 significantly reduced the number of FA-like HSPCs with γH2AX and 53BP1 foci (Figure 5L, 5M, S5F and S5G), suggesting that TGF-β pathway inhibition improves DNA repair in these primary human FA-like HSPCs. Together, our data indicate that the TGF-β signaling is increased in human FA HSPCs and that blockade of this pathway partially restores their function. TGF-β Pathway Inhibition Upregulates HR and Downregulates NHEJ in HSCs of FA Mice
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To determine the molecular mechanism by which TGF-β pathway regulates DNA repair and rescues genotoxicity in HSCs, we next analyzed the expression of DNA repair genes in HSCs. Genes associated with NHEJ, HR, nucleotide excision repair (NER), mismatch repair (MMR), and the DNA damage response (DDR) were evaluated. Interestingly, over 70% of DNA repair genes examined were significantly upregulated in HSCs from WT mice exposed to 1D11, the neutralizing anti-murine TGF-β monoclonal antibody (Figure 6A and S6A). In contrast, many genes involved in NHEJ were upregulated and many genes involved in HR were downregulated in HSCs from Fancd2−/− mice, when compared to WT HSCs (Figure 6B). This skewed expression pattern in Fancd2−/− HSCs was reversed by TGF-β pathway Cell Stem Cell. Author manuscript; available in PMC 2017 May 05.
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inhibition, as 1D11 antibody treatment induced expression of HR genes such as Brca2 and Xrcc1 in Fancd2−/− HSCs, and caused a concomitant reduction of NHEJ gene expression, such as Lig4 and Prkdc (Figure 6C–6E). Previous studies have shown that HR is upregulated when HSCs are driven into the cell cycle, thereby resulting in repair of double strand breaks (Beerman et al., 2014). Accordingly, the increase in HR activity in FA HSCs following TGFβ pathway inhibition may result, at least in part, from the release from cell cycle arrest (Figure S6B), subsequently leading to a higher frequency of HSCs in FA mice (Figure 6F). To confirm that inhibition of TGF-β pathway in HSCs creates an HR-competent state and thereby functionally protects them from genotoxicity, we inhibited both HR and TGF-β pathway and examined the survival of cells after acetaldehyde exposure (Figure 6G). We used pharmacologic inhibitors which blocked HR, resulting in the reduction of RAD51 foci and the inhibition of DR-GFP plasmid recombination in a reporter assay (Figure S6D–S6F). As expected, 1D11 exposure inhibited TGF-β pathway signaling in bone marrow from FA mice (Figure S6C). Interestingly, 1D11 did not protect the HSPCs from acetaldehydeinduced genotoxicity when HR was inhibited by pharmacologic inhibitors of RAD51 (Budke et al., 2012; Huang et al., 2012) (Figure 6H, S6G and S6H). Collectively, these data indicate that TGF-β pathway inhibition upregulates HR and downregulates NHEJ in HSPCs of Fancd2−/− mice and functionally promotes their survival. TGF-β Pathway Inhibition Increases HR and Decreases NHEJ in FA Cells
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To directly confirm that inhibition of TGF-β pathway modulates HR or NHEJ activity, we engineered an individual DNA breakpoint in FA (GM6914) cells and employed the traffic light reporter (TLR) system which quantifies both HR and NHEJ activities (Certo et al., 2011). In the TLR assay, double strand break (DSB) generated by I-Sce1 endonuclease can be repaired by either HR or NHEJ pathway when the donor repair template is provided, however, the DSB can be repaired by NHEJ only when the repair template is missing (Figure S7A). NHEJ and not HR activity was observed in FA cells when the donor repair template was missing (Figure S7B), validating the assay. As predicted, FA (GM6914) cells exhibited fewer HR events compared to the FA-A-corrected (GM6914+FANCA) cells (Figure 7A). Interestingly, TGF-β pathway inhibition, by knockdown of SMAD3, in FA cells resulted in increased HR events with a concomitant decrease in NHEJ events (Figure 7A and 7B). Inhibition of TGF-β pathway by the small molecule inhibitor SD208 also resulted in increased HR activity in FA cells (Figure 7C). Similar findings were revealed when different reporter systems were used to quantify the HR and NHEJ activities individually (Figure 7D and 7E). Consistently, knockdown of SMAD3 in FA cells resulted in decreased phosphorylation of DNA-PK, a marker of NHEJ (Figure S7C). Additionally, damageinduced RAD51 foci resolved more quickly in SMAD3-depleted FA cells (Figure 7F and 7G), implying that HR-mediated DNA repair is more efficient in these cells. Analysis of the genome-wide siRNA screening data (Adamson et al., 2012) revealed that siRNA-mediated knockdown of several TGF-β pathway genes enhanced HR activity (Figure S7D). Taken together, these data indicate that TGF-β pathway inhibition promotes DNA repair by directly increasing HR activity in FA cells.
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DISCUSSION
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Although the pathophysiology of BMF in FA is poorly understood, anemia in FA patients is known to result from attrition of HSPCs. The attrition of HSPCs in FA results from multiple mechanisms including impaired HSPC function, genotoxicity in HSPCs from the endogenous crosslinking agent, acetaldehyde (Garaycoechea et al., 2012; Langevin et al., 2011), physiological stress (Walter et al., 2015), elevated p53 levels in HSPCs (Ceccaldi et al., 2012), and hypersensitivity of the bone marrow to inflammatory cytokines (Haneline et al., 1998; Li et al., 2007). Here, we show that hyperactive TGF-β signaling also contributes to the impairment of the HSPC function in FA bone marrow. Blocking of TGF-β pathway signaling in FA HSPCs improves their growth and survival under genotoxic stress. TGF-β pathway inhibition in FA cells reduces toxic NHEJ and partially rescues HR activity. Hyperactive NHEJ is known to be toxic to FA cells, and NHEJ inhibitors improve FA cell growth (Adamo et al., 2010; Pace et al., 2010). Thus, the improved growth of FA HSPCs following TGF-β pathway inhibition appears to result largely from restored HR repair and reduced NHEJ repair, resulting in part from an increase in cycling HSPCs. TGF-β inhibition also appears to promote a HR competent state, even in cells which have not entered active cycling. Under physiological stress, the rapid reduction in DNA damage by TGF-β inhibition results in a rapid decline in cycling and in the maintenance or, for some cells, the return to an HSC quiescent state. Our results also support the recent finding that DNA damage accumulation occurs in quiescent, but not cycling HSCs (Beerman I et al, 2014).
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Our study shows that mutation in FA genes results in hyperactive TGF-β signaling. This result suggests that the FA pathway normally functions to activate FANCD2 and to repress transcription of SMAD genes. We show that FANCD2, a critical downstream component of the FA pathway, binds to the promoter region of SMAD1. Activated FANCD2 has been previously reported to decrease transcription of the TNFα gene and to increase transcription of the TAp63 gene (Matsushita et al., 2011; Park et al., 2013). Our results indicate that hyperactive TGF-β pathway in FA cells contributes to the impairment of DNA repair due to downregulation of HR activity. The TGF-β pathway is known to play a role in DNA damage response (Barcellos-Hoff and Cucinotta, 2014). For instance, BRCA2 and SMAD3 form a complex and synergize in regulation of gene transcription (Preobrazhenska et al., 2002). SMAD3 also counteracts BRCA1-dependent repair of DNA double-strand breaks in human breast epithelial cells (Dubrovska et al., 2005). In addition, TGF-β pathway induces HR defects in breast cancer cells by regulating BRCA1, ATM, and MSH2 DNA repair genes (Liu et al., 2014). Moreover, TGF-β pathway activation promotes genomic instability by downregulating RAD51 protein expression in lung epithelial cells (Kanamoto et al., 2002). These studies further support our finding that inhibition of the hyperactive TGF-β pathway restores HR in FA HSPCs and improves their function. It remains to be determined whether the SMAD factors directly suppress HR gene transcription and promote NHEJ gene transcription. Our results elucidate a mechanism that contributes to bone marrow failure in FA patients– namely, the increased TGF-β signaling in FA HSPCs. TGF-β is a myelosuppressive cytokine that has been also implicated in the hematopoietic suppression of other hematopoietic diseases, including myelodysplastic syndrome (MDS), suggesting a more general
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mechanism of BMF (Suragani et al., 2014; Zhou et al., 2011; Zingariello et al., 2013). Plasma levels of TGF-β are mildly upregulated in MDS patients, and increased TGF-β immunohistochemical staining is evident in the bone marrow. Inhibition of TGF-β pathway after chemotherapy accelerates hematopoietic reconstitution by delaying the return of cycling HSCs to quiescence (Brenet et al., 2013). Murine and human FA HSPC function was enhanced after TGF-β pathway inhibition, consistent with the notion that TGF-β regulates quiescence and self-renewal of HSPCs (Bank and Kalrsson, 2014).
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Finally, our findings have implications for the clinical care of FA patients. Pharmacological agents targeting the TGF-β pathway have been developed for a variety of disease conditions, and some have shown efficacy in preclinical murine models and in human phase I and II clinical trials (Akhurst and Hata, 2012; Grafe et al., 2014; Suragani et al., 2014). Pharmacological inhibition of the TGF-β pathway appears to be safe and well tolerated, and 1D11 treatment does not cause obvious negative effects on general health, behavior, or growth in mice (Grafe et al., 2014). Inhibition of the TGF-β pathway may also be a clinically useful strategy during gene therapy for ex vivo expansion of rare HSPCs derived from FA patients (Rio et al., 2014). Additionally, the ability of TGF-β pathway inhibition to increase HR and decrease NHEJ may also provide a tool to improve CRISPR-mediated genome editing and may also be a mechanistic basis for the reduction of tumorigenesis.
EXPERIMENTAL PROCEDURES Detailed procedures can be found in the Supplemental Experimental Procedures. Genome-wide shRNA Screen
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The screen was performed using the Hannon-Elledge whole genome pooled shRNA library as previously described (Luo et al., 2009). Mice
Fancd2−/− mice in C57BL/6J background are previously described (Parmar et al., 2010). B6.SJL-PtprcaPep3b/BoyJ (Congenic B6, CD45.1+) mice and NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ (NSG) mice were purchased from The Jackson Laboratory. All experimental procedures were approved by the Animal Care and Use Committee of the Dana Farber Cancer Institute. Hematopoietic Stem/progenitor Cell Culture And Flow Cytometry Analysis
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The procedures of enrichment and cell staining for isolating HSPCs (Lin−cKit+Sca-1+) and HSCs (Lin−cKit+Sca-1+CD48−CD150+) from mouse bone marrow were performed as described (Zhang et al., 2012). Murine Bone Marrow Transplantation Donor cells (CD45.2+) were transplanted into lethally irradiated (10 Gy dose) recipient (congenic B6-CD45.1+ mice) along with 1×105cells competitive bone marrow cells from congenic B6-CD45.1+ mice. Peripheral blood from recipient mice was analyzed for donor cell engraftment as described (Parmar et al., 2010).
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Colony-forming Unit-spleen (CFU-S) Assay
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Recipient mice (wild-type, 8–12 weeks old) were irradiated with a split dose of 1100 rad (550 rad each, 4 hours apart) before transplantation. Forty thousand bone marrow cells from donor mice were transplanted into each recipient mouse. Ten to 12 days post-transplantation, spleens were harvested and fixed with Bouin fixative solution. In Vivo Xenograft Assay
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Human cord blood derived CD34+ cells were transduced with lentivirus encoding shFANCD2 or shControl as described (Ceccaldi et al., 2012). While cells were selected with 2μg/mL puromycin, cells were also treated with 10μg/mL GC1008. After 48h treatment, 2×105 cells were transplanted into sub-lethally irradiated (2.5Gy) NSG mice. The recipient mice were treated with 10mg/kg GC1008 at 3 doses per week for two weeks. Two and eight weeks after transplantation, human cells in peripheral blood (PB) were analyzed using antihuman CD45 antibody (eBioscience, 17–0459–42) by flow cytometry. Statistics Two-tailed P values for statistical analysis were obtained using Student’s t-test.
Supplementary Material Refer to Web version on PubMed Central for supplementary material.
Acknowledgments Author Manuscript
We are grateful to Raphael Ceccaldi and members of our laboratory for helpful discussion. We thank Benjamin Primack for maintaining Fancd2 mouse colony. We thank Dr. H. Lin (Massachusetts General Hospital), who generously provided the TGF-β reporter CAGA-Luciferase plasmid. We thank Genzyme Corp for providing the 1D11 and GC1008 antibodies. We thank the FA patients and their families. H.Z is supported by the Leukemia & Lymphoma Society Fellow Award. This work was also supported by grants from U.S. National Institutes of Health R01DK43889, R37HL052725 (to A.D.), and P01HL048546 (to M.G.).
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Figure 1. TGF-β Pathway Disruption Enhances Human FA Cellular Growth under Genotoxic Stress
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(A) RIGER P value analysis to identify top candidate genes in genome-wide screen. Top candidates are highlighted with different colors. Genes of the TGF-β pathway (BMP2, SMAD3, PDCD4) are pointed out by arrow. Genes involved in MMC metabolism (NQO1 and NFE2L2) are pointed out by arrowhead. (B) Clonogenic survival of GM6914 (FA-A fibroblasts) and FANCA-corrected GM6914 cells after shRNA mediated knockdown of SMAD3. Cells were exposed MMC and cell survival was determined after 10–12 days in culture. The average of two independent experiments is presented. Immunoblot in the right panel shows SMAD3 knockdown efficiency in GM6914 cells. (C,D) MMC sensitivity of EUFA316 (FA-G lymphoblasts) and FANCG-corrected EUFA316 cells incubated with or without 10μM SMAD3 inhibitor SIS3 or 10μM TGF-β inhibitor SD208. Cells were cultured in triplicates in presence of MMC and DMS0 or inhibitor for 5– 6 days and survival was determined. Data are representative of 3 independent experiments. (E) Acetaldehyde sensitivity of EUFA316 and FANCG-corrected EUFA316 cells incubated with or without 10μM SD208. Cells were exposed to acetaldehyde for 3 hours and survival
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was determined after culturing them for 5–6 days in presence of DMSO or SD208 in triplicates. The data are representative of 3 independent experiments. (F) Acetaldehyde sensitivity of EUFA316 cells after shRNA mediated knockdown SMAD3 and TP53. Right panel shows the immunoblots of the lysates from EUFA316 cells showing shRNA-mediated knockdown of SMAD3 or p53. Error bars represent mean ± s.e.m. *, p
Cell Stem Cell. Author manuscript; available in PMC 2017 May 05. Published in final edited form as: Cell Stem Cell. 2016 May 5; 18(5): 668–681. doi:10.1016/j.stem.2016.03.002.
TGF-β Inhibition Rescues Hematopoietic Stem Cell Defects and Bone Marrow Failure in Fanconi Anemia Haojian Zhang1, David E Kozono1, Kevin W O’Connor1, Sofia Vidal-Cardenas1, Alix Rousseau2, Abigail Hamilton1, Lisa Moreau1, Emily F Gaudiano1, Joel Greenberger3, Grover Bagby4, Jean Soulier2, Markus Grompe4, Kalindi Parmar1, and Alan D D’Andrea1 1Department
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2Institute
of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA
of hematology (IUH), University Paris-Diderot, Sorbonne Paris Cite 75010
3Department
of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA
15213, USA 4Oregon
Health and Science University, Portland, OR 97239, USA
SUMMARY
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Fanconi Anemia (FA) is an inherited DNA repair disorder characterized by progressive bone marrow failure (BMF) from hematopoietic stem and progenitor cell (HSPC) attrition. A greater understanding of the pathogenesis of BMF could improve the therapeutic options for FA patients. Using a genome-wide shRNA screen in human FA fibroblasts, we identify transforming growth factor-β (TGF-β) pathway-mediated growth suppression as a cause of BMF in FA. Blocking the TGF-β pathway improves the survival of FA cells and rescues the proliferative and functional defects of HSPCs derived from FA mice and FA patients. Inhibition of TGF-β signaling in FA HSPCs results in elevated homologous recombination (HR) repair with a concomitant decrease in non-homologous end-joining (NHEJ), accounting for the improvement in cellular growth. Together, our results suggest that elevated TGF-β signaling contributes to the BMF in FA by impairing HSPC function, and may be a potential therapeutic target for the treatment of FA.
INTRODUCTION Hematopoietic stem cells (HSCs) replenish the blood system throughout the life span of an organism and maintain homeostasis. Consequently, depletion or impairment of the HSC
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Corresponding Author: Alan D. D’Andrea, M.D., Director: Center for DNA Damage and Repair, The Fuller-American Cancer Society Professor, Harvard Medical School, Chief, Division of Genomic Stability and DNA Repair, Department of Radiation Oncology and Pediatrics, Dana-Farber Cancer Institute, Mayer 640, 450 Brookline Ave., Boston, MA 02215, 617-632-2080, FAX: 617-632-5757, [email protected]. AUTHOR CONTRIBUTIONS H.Z. and A.D.D designed experiments. H.Z., D.E.K., K.W.O., S.V., A.R., A.H., L.M., E.F.G., and K.P., performed experiments with help from J.G., G.B., J.S., and M.G.. H.Z., D.E.K., K.P., and A.D.D. analyzed and interpreted the data. H.Z., K.P., and A.D.D. wrote the manuscript. Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
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reservoir leads to hematopoietic failure or hematologic malignancies. Accumulation of DNA damage and genomic instability, due to physiological stress or exposure to genotoxic agents, is one of the mechanisms of loss of HSC reserve (Garaycoechea et al., 2012; Mandal et al., 2011; Walter et al., 2015). Protective cellular DNA repair mechanisms exist in HSCs to combat the accumulation of DNA damage. Accordingly, the genetic ablation of proteins (e.g. Atm, Lig4, ATR) involved in DNA repair pathways in mice results in severe HSC defects (Ito et al., 2006; Niedernhofer, 2008; Rossi et al., 2007; Ruzankina et al., 2007), and the NHEJ pathway is the most commonly used DNA repair mechanism in quiescent HSCs (Milyavsky et al., 2010; Mohrin et al., 2010).
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Fanconi anemia (FA) is the most common inherited bone marrow failure (BMF) syndrome. FA patients develop progressive bone marrow failure during childhood. In addition, FA patients also develop other hematologic manifestations, including myelodisplastic syndrome (MDS) and acute myeloid leukemia (AML) due to clonal evolution (Shimamura and Alter, 2010). Current therapies for hematologic manifestations in FA include hematopoietic stem cell transplant and treatment with growth factors and androgens. While an allogenic bone marrow transplant from a histocompatible sibling donor remains the optimal long-term therapy, many FA patients do not have a suitable donor. Moreover, transplant may contribute to increased incidence of later, non-hematologic consequence such as secondary solid tumors and endocrine failure (Shimamura and Alter, 2010). Therefore, novel alternative treatment options to treat marrow failure in FA patients are needed.
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FA is caused by biallelic mutation in one of eighteen FANC genes (FANC-A, B, C, D1, D2, E, F, G, I, J, L, M, N, O, P, Q, S, T), the products of which cooperate in the FA/BRCA DNA repair pathway and regulate cellular resistance to DNA cross-linking agents (Kottemann and Smogorzewska, 2013; Sawyer et al., 2015). Due to the underlying DNA repair defect, FA cells are hypersensitive to genotoxic DNA crosslinking agents. Although the precise biochemical functions of the FA/BRCA pathway in DNA repair remain unclear, the pathway promotes homologous recombination (HR) repair (Deans and West, 2011). The FA/BRCA pathway also regulates cytokinesis, and pathway disruption results in increased binucleate bone marrow cells and apoptosis (Chan et al., 2009; Naim and Rosselli, 2009; Vinciguerra et al., 2010). FA cells are also uniquely hypersensitive to oxidative stress and apoptotic cytokines, such as IFNγ and TNFα (Pang and Andreassen, 2009).
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All blood lineages are deficient in FA patients (Butturini et al., 1994), suggesting that the FA pathway regulates the function of hematopoietic stem and progenitor cells (HSPCs). Accordingly, recent studies indicate that the BMF in FA is attributable to an impaired HSPC pool. HSPCs in FA patients and FA mice exhibit reduced cell number and compromised stem cell function (Ceccaldi et al., 2012; Crossan et al., 2011; Parmar et al., 2009; Parmar et al., 2010; Zhang et al., 2010). The primary mechanism of the impairment of HSPCs leading to the BMF in FA, however, remains elusive. Due to the well-defined role of the FA/BRCA pathway in repairing DNA damage (Deans and West, 2011; Kottemann and Smogorzewska, 2013), DNA damage accumulation in HSPCs may be one of the major causes for BMF in FA. Indeed, recent studies suggest that BMF in FA and impaired HSPC function result from the genotoxicity of endogenous crosslinking agents or from physiological stress (Garaycoechea et al., 2012; Langevin et al., 2011; Walter et al., 2015). Bone marrow failure
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in FA may also result, directly or indirectly, from hyperactivation of cell autonomous or microenvironmental growth suppressive pathways, induced in part, due to genotoxic stress. We have recently shown that one suppressive mechanism results from a hyperactive p53 response in HSPCs from FA patients (Ceccaldi et al., 2012). Here, we performed an unbiased shRNA screen to identify additional growth suppressive pathways which may account for the impairment/attrition of the FA bone marrow HSPCs. We identified hyperactive TGF-β signaling in HSPCs as a mechanism of bone marrow suppression in FA. Disruption of TGF-β signaling significantly protected HSCs in FA from genotoxic stress by increasing HR activity and decreasing NHEJ activity.
RESULTS TGF-β Pathway Blocks FA Cell Survival in the Presence of Genotoxic Agents
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We initially performed a genome-wide shRNA screen in a patient-derived FANCA−/− fibroblast line in order to identify genes whose knockdown can rescue the FA phenotype in the presence of a genotoxic agent, Mitomycin C (MMC) (Figure S1A and S1B). Multiple TGF-β pathway genes (e.g. SMAD3, BMP2, PDCD4) were among the top hits (Figure 1A). shRNAs targeted against NQO1 and NFE2L2 genes involved in MMC metabolism (Siegel et al., 2012) also scored positive (Figure 1A), validating our screen for MMC resistance. The TGF-β pathway is known to contribute to hematopoietic suppression in other human diseases, such as myelodysplastic syndrome (MDS) (Suragani et al., 2014; Zhou et al., 2011; Zingariello et al., 2013), suggesting a more general mechanism in BMF. We next validated our primary screening data in a number of FA cell lines. The respective cell lines, which were corrected by reconstitution with FANCA or FANCG cDNAs, were used as positive controls as they were more resistant to MMC compared to the uncorrected FA cells (Figure 1B–1D). Both knockdown of SMAD3 and pharmacologic inhibition of the TGF-β pathway with small molecules, SD208 and SIS3, significantly enhanced the survival of FA cells in the presence of MMC (Figure 1B–1D, and S1C).
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DNA damage caused by an endogenous genotoxic agent, acetaldehyde, requires the FA pathway for repair (Garaycoechea et al., 2012). Accordingly, we identified an FA patientderived FANCG-deficient lymphoblast line, EUFA316, which is hypersensitive to acetaldehyde (Figure S1D). Both pharmacologic inhibition by SD208 and genetic depletion by shRNA of the TGF-β pathway promoted cellular survival in the presence of acetaldehyde (Figure 1E and 1F). Additionally, disruption of the TGF-β pathway by shRNA or by SD208 resulted in reduced p53 and p21 protein levels (Figure S1E). Together, these data demonstrate that targeting the TGF-β pathway can reduce the genotoxic stress mediated growth inhibition of human FA cells. TGF-β Pathway Inhibition Rescues the Functional Defects of HSCs from FA Mice As FA mice exhibit HSPC defects, the possible suppressive function of the TGF-β pathway in bone marrow HSPCs of FA mice was next examined. Elevated expression levels of both Tgfb1 and Smad3 were observed in Fancd2−/− HSPCs [Lin−Sca-1+c-Kit+ (LSK) population] (Figure 2A). Elevated pSmad2/3 protein levels were also observed in Fancd2−/− HSPCs (Figure S2A and S2B). Moreover, enhanced mRNA expression of TGF-β pathway target
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genes, including Cdkn1a, Cdkn1c, Foxp3, and Atg5, was also observed in Fancd2−/− HSPCs (Figure 2A), implying that the TGF-β pathway is upregulated in FA HSPCs. Fancd2−/− bone marrow HSPCs were more sensitive to TGF-β1 than wild-type HSPCs (Figure S2C). Therefore, we hypothesized that inhibition of this pathway might rescue the defect of FA HSPCs. Colony forming assays showed that the clonogenic ability of Fancd2−/− HSPCs was inhibited by TGF-β1; blockade of the TGF-β signaling by 1D11 (a neutralizing antibody against mouse TGF-β) (Brenet et al., 2013) or SD208 markedly enhanced the clonogenic ability (Figure S2D–S2F). Further, genetic knockdown of Smad3 promoted the in vitro expansion of HSPCs and in vivo engraftment of Lin− cells from bone marrow of Fancd2−/− mice (Figure 2B, 2C, and S2G–S2J). Taken together, inhibition of the TGF-β pathway can rescue the functional defects of Fancd2−/− HSPCs.
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Hyperactive TGF-β pathway signaling in Fancd2−/− HSPCs prompted us to assess whether the FA pathway components directly transcriptionally regulate the expression of TGF-β pathway genes. We first confirmed that mutation in FA genes results in hyperactive TGF-β activity. We transfected a TGF-β luciferase reporter vector containing SMAD binding element, into FA cells or corrected FA cells. Interestingly, increased TGF-β luciferase activity was observed in FA-A cells compared to FANCA-corrected cells (Figure S2K). Conversely, overexpression of FANCD2 in 293T cells significantly reduced the TGF-β luciferase reporter activity (Figure 2D). Using chromatin immunoprecipitation (ChIP) assays, we previously showed that activated FANCD2 increases the transcriptional activity of the TAp63 gene (Park et al., 2013). A genome-wide ChIP sequencing (ChIP-seq) analysis, using FANCD2 antibody, demonstrated that FANCD2 also binds to SMAD gene promoters (Park et al., 2013). ChIP confirmed that FANCD2 can directly bind to the promoter region of a SMAD gene, suggesting that FANCD2 decreases the transcriptional activity of SMAD genes. Interestingly, FANCD2 bound to the promoter of SMAD1 in 293T cells (Figure 2E). The binding of FANCD2 to the promoter of SMAD1 was observed in corrected FA cells, but not in the parental FA cells (EUFA316 and GM6914), suggesting that a functional FA pathway is required for the FANCD2-mediated transcriptional decrease of the TGFβ pathway gene (Figure 2F and S2L). Collectively, these results demonstrate that disruption of the FA pathway causes transcriptional changes, resulting in hyperactive TGF-β signaling. TGF-β Pathway Inhibition Rescues Acetaldehyde-induced Genotoxicity in HSPCs from FA Mice
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DNA damage induced by the endogenous genotoxic agents, such as acetaldehyde, causes the attrition of HSCs, leading to spontaneous bone marrow failure in murine FA models (Garaycoechea et al., 2012; Langevin et al., 2011). We reasoned that blockade of the TGF-β pathway may contribute to the repair of acetaldehyde-induced DNA damage in FA HSCs. As expected, bone marrow cells from Fancd2−/− mice were sensitive to acetaldehyde exposure. The neutralizing anti-TGF-β antibody 1D11 treatment counteracted the genotoxic effects of acetaldehyde, and rescued the growth and clonogenic capacity of Fancd2−/− HSCs or Lin− cells from bone marrow (Figure 3A and S3A). To directly measure the protective effect of 1D11 on the survival of HSPCs after acetaldehyde exposure, a stem cell transplant was performed. The percentage of donor-derived cells at 4 and 16 weeks post transplantation was higher in recipients of 1D11 treated Fancd2−/− group than those in the isotype control group
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(Figure 3B and S3B), and 1D11 did not significantly affect the lineage differentiation of HSPCs (Figure S3C). Furthermore, γH2AX foci, a marker for DNA damage, resolved more rapidly in 1D11 treated Fancd2−/− cells, suggesting an improvement of DNA repair (Figure 3C, 3D, and S3D). Repair of DNA damage was further confirmed by comet assay (Figure 3E, 3F, and S3E). 1D11 treated Fancd2−/− cells also showed improvement in DNA repair when DNA damage was directly assessed by alkaline comet assay and confirmed that acetaldehyde-induced γH2AX foci indeed correspond to unrepaired double strand breaks (Figure 3E, 3F, and S3E), Taken together, pharmacologic inhibition of the TGF-β pathway by 1D11 promotes resistance of FA cells to endogenous genotoxic agents, and partially corrects the impaired stem cell function by promoting DNA repair. Inhibition of TGF-β Pathway Rescues Physiological Stress-induced Bone Marrow Failure in FA Mice
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Physiological stress-induced DNA damage is a source of DNA damage in HSCs in FA. The accumulation of physiological stress-induced DNA damage results in a collapse of the hematopoietic system in a murine FA model (Walter et al., 2015). Interestingly, polyinosinic:polycytidylic acid (pI:pC) exposure caused activation of TGF-β pathway in HSPCs (Figure S4A). To determine whether inhibition of TGF-β pathway also counteracts the genomic instability of HSCs caused by physiological stress, we simultaneously treated WT and Fancd2−/− mice for 48h with pI:pC (to induce stress) and 1D11 (to block the TGF-β pathway). As previously described (Walter et al., 2015), administration of pI:pC induced DNA damage in HSCs and caused increased levels of γH2AX and 53BP1 foci (Figure 4A– 4D and S4B); inhibition of the TGF-β pathway by 1D11 markedly reduced the pI:pCinduced DNA damage (Figure 4A–4D, S4B, and S4C). Importantly, inhibition of the TGF-β pathway rescued the viability of Fancd2−/− total bone marrow cells following pI:pC treatment (Figure S4D). Consistent with the previous study (Walter et al., 2015), pI:pC exposure induced oxidative stress in HSPCs from Fancd2−/− mice, however, 1D11 did not affect the level of oxidative stress (Figure S4E). As expected, pI:pC exposure induced proliferation of HSPCs, resulting in a concomitant reduction in the frequencies of quiescent cells. Interestingly, 1D11 treatment reduced pI:pC-induced cell cycling and increased the percentage of quiescent HSPCs, perhaps accounting for the improved DNA repair (Figure S4F). Thus, TGF-β pathway inhibition counteracts physiological stress-induced DNA damage in HSCs.
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To determine whether TGF-β pathway inhibition rescues pI:pC induced bone marrow failure, we treated WT and Fancd2−/− mice with pI:pC and 1D11 (Figure 4E). Interestingly, four weeks of pI:pC treatment caused peripheral blood pancytopenia in isotype control antibody-treated Fancd2−/− mice with reduction in red blood cells (RBC), white blood cells (WBC) and hemoglobin levels (Figure 4F). However, administration of 1D11 significantly prevented these peripheral blood abnormalities (Figure 4F). To examine the bone marrow HSC function, we next transplanted bone marrow cells from these pI:pC (plus or minus 1D11) treated donor mice into lethally irradiated recipients and evaluated spleen colonyforming units (CFU-S), thus allowing the quantification of the surviving multipotent shortterm HSCs. As expected, pI:pC treatment caused a marked reduction in the CFU-S content of Fancd2−/− bone marrow, and 1D11 improved this defect (Figure 4G). Consistent with
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these results, in a competitive repopulation experiment, recipient mice transplanted with bone marrow from 1D11 treated Fancd2-/- mice showed improved short-term donor cell engraftment compared to the recipients transplanted with isotype control (Figure 4H). Bone marrow HSPCs from Fancd2−/− mice treated with 1D11 also exhibited less DNA damage upon pI:pC exposure (Figure 4I, 4J, and S4G). Together, these data suggest that TGF-β pathway inhibition rescues pI:pC-induced bone marrow failure in FA mice and may be effective in preventing the bone marrow collapse of FA patients observed after viral infections. TGF-β Pathway Inhibition Restores the Function of HSPCs Derived from Humans with FA
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We next extended our studies in HSPCs derived from patients with FA. Primary human FA bone marrow cells demonstrated increased mRNA expression of multiple TGF-β pathway components (Figure 5A and S5A). TGF-β pathway inhibition, by knockdown of SMAD3 or by exposure to anti-human TGF-β neutralizing antibody GC1008, rescued the clonogenic defects of primary HSPCs from bone marrow of FA patients, although to a lesser extent than the rescue observed following p53 knockdown (Figure 5B–5F and S5B). Variable response to TGF-β pathway inhibition in primary human FA patient HSPCs may result from differences in the age, gender, intrinsic genetic differences, the levels of SMAD3/p53 in HSPCs, or the severity of the pre-existing bone marrow failure. Depletion of SMAD3 in FAlike primary HSPCs established by FANCD2 knockdown in human cord blood CD34+ cells, also rescued their clonogenicity, and partially restored MMC resistance (Figure 5G–5I and S5C). Inhibition of TGF-β signaling by GC1008 also recapitulated this phenotype by markedly rescuing the clonogenic capacity of FA-like HSPCs (Figure 5J and S5D). Further, since the very low CD34+ cell numbers in FA patients did not allow efficient xenograft assays for analysis of clonogenicity in vivo, we performed a surrogate in vivo xenograft assay using FA-like CD34+ cells. Strikingly, GC1008 treatment in vivo enhanced the engraftment of primary FA-like CD34+ cells (Figure 5K and S5E). In addition, we observed a higher frequency of FA-like HSPCs with γH2AX and 53BP1 foci upon MMC exposure, compared to the control HSPCs (Figure 5L, 5M, S5F and S5G). Exposure to GC1008 significantly reduced the number of FA-like HSPCs with γH2AX and 53BP1 foci (Figure 5L, 5M, S5F and S5G), suggesting that TGF-β pathway inhibition improves DNA repair in these primary human FA-like HSPCs. Together, our data indicate that the TGF-β signaling is increased in human FA HSPCs and that blockade of this pathway partially restores their function. TGF-β Pathway Inhibition Upregulates HR and Downregulates NHEJ in HSCs of FA Mice
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To determine the molecular mechanism by which TGF-β pathway regulates DNA repair and rescues genotoxicity in HSCs, we next analyzed the expression of DNA repair genes in HSCs. Genes associated with NHEJ, HR, nucleotide excision repair (NER), mismatch repair (MMR), and the DNA damage response (DDR) were evaluated. Interestingly, over 70% of DNA repair genes examined were significantly upregulated in HSCs from WT mice exposed to 1D11, the neutralizing anti-murine TGF-β monoclonal antibody (Figure 6A and S6A). In contrast, many genes involved in NHEJ were upregulated and many genes involved in HR were downregulated in HSCs from Fancd2−/− mice, when compared to WT HSCs (Figure 6B). This skewed expression pattern in Fancd2−/− HSCs was reversed by TGF-β pathway Cell Stem Cell. Author manuscript; available in PMC 2017 May 05.
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inhibition, as 1D11 antibody treatment induced expression of HR genes such as Brca2 and Xrcc1 in Fancd2−/− HSCs, and caused a concomitant reduction of NHEJ gene expression, such as Lig4 and Prkdc (Figure 6C–6E). Previous studies have shown that HR is upregulated when HSCs are driven into the cell cycle, thereby resulting in repair of double strand breaks (Beerman et al., 2014). Accordingly, the increase in HR activity in FA HSCs following TGFβ pathway inhibition may result, at least in part, from the release from cell cycle arrest (Figure S6B), subsequently leading to a higher frequency of HSCs in FA mice (Figure 6F). To confirm that inhibition of TGF-β pathway in HSCs creates an HR-competent state and thereby functionally protects them from genotoxicity, we inhibited both HR and TGF-β pathway and examined the survival of cells after acetaldehyde exposure (Figure 6G). We used pharmacologic inhibitors which blocked HR, resulting in the reduction of RAD51 foci and the inhibition of DR-GFP plasmid recombination in a reporter assay (Figure S6D–S6F). As expected, 1D11 exposure inhibited TGF-β pathway signaling in bone marrow from FA mice (Figure S6C). Interestingly, 1D11 did not protect the HSPCs from acetaldehydeinduced genotoxicity when HR was inhibited by pharmacologic inhibitors of RAD51 (Budke et al., 2012; Huang et al., 2012) (Figure 6H, S6G and S6H). Collectively, these data indicate that TGF-β pathway inhibition upregulates HR and downregulates NHEJ in HSPCs of Fancd2−/− mice and functionally promotes their survival. TGF-β Pathway Inhibition Increases HR and Decreases NHEJ in FA Cells
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To directly confirm that inhibition of TGF-β pathway modulates HR or NHEJ activity, we engineered an individual DNA breakpoint in FA (GM6914) cells and employed the traffic light reporter (TLR) system which quantifies both HR and NHEJ activities (Certo et al., 2011). In the TLR assay, double strand break (DSB) generated by I-Sce1 endonuclease can be repaired by either HR or NHEJ pathway when the donor repair template is provided, however, the DSB can be repaired by NHEJ only when the repair template is missing (Figure S7A). NHEJ and not HR activity was observed in FA cells when the donor repair template was missing (Figure S7B), validating the assay. As predicted, FA (GM6914) cells exhibited fewer HR events compared to the FA-A-corrected (GM6914+FANCA) cells (Figure 7A). Interestingly, TGF-β pathway inhibition, by knockdown of SMAD3, in FA cells resulted in increased HR events with a concomitant decrease in NHEJ events (Figure 7A and 7B). Inhibition of TGF-β pathway by the small molecule inhibitor SD208 also resulted in increased HR activity in FA cells (Figure 7C). Similar findings were revealed when different reporter systems were used to quantify the HR and NHEJ activities individually (Figure 7D and 7E). Consistently, knockdown of SMAD3 in FA cells resulted in decreased phosphorylation of DNA-PK, a marker of NHEJ (Figure S7C). Additionally, damageinduced RAD51 foci resolved more quickly in SMAD3-depleted FA cells (Figure 7F and 7G), implying that HR-mediated DNA repair is more efficient in these cells. Analysis of the genome-wide siRNA screening data (Adamson et al., 2012) revealed that siRNA-mediated knockdown of several TGF-β pathway genes enhanced HR activity (Figure S7D). Taken together, these data indicate that TGF-β pathway inhibition promotes DNA repair by directly increasing HR activity in FA cells.
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DISCUSSION
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Although the pathophysiology of BMF in FA is poorly understood, anemia in FA patients is known to result from attrition of HSPCs. The attrition of HSPCs in FA results from multiple mechanisms including impaired HSPC function, genotoxicity in HSPCs from the endogenous crosslinking agent, acetaldehyde (Garaycoechea et al., 2012; Langevin et al., 2011), physiological stress (Walter et al., 2015), elevated p53 levels in HSPCs (Ceccaldi et al., 2012), and hypersensitivity of the bone marrow to inflammatory cytokines (Haneline et al., 1998; Li et al., 2007). Here, we show that hyperactive TGF-β signaling also contributes to the impairment of the HSPC function in FA bone marrow. Blocking of TGF-β pathway signaling in FA HSPCs improves their growth and survival under genotoxic stress. TGF-β pathway inhibition in FA cells reduces toxic NHEJ and partially rescues HR activity. Hyperactive NHEJ is known to be toxic to FA cells, and NHEJ inhibitors improve FA cell growth (Adamo et al., 2010; Pace et al., 2010). Thus, the improved growth of FA HSPCs following TGF-β pathway inhibition appears to result largely from restored HR repair and reduced NHEJ repair, resulting in part from an increase in cycling HSPCs. TGF-β inhibition also appears to promote a HR competent state, even in cells which have not entered active cycling. Under physiological stress, the rapid reduction in DNA damage by TGF-β inhibition results in a rapid decline in cycling and in the maintenance or, for some cells, the return to an HSC quiescent state. Our results also support the recent finding that DNA damage accumulation occurs in quiescent, but not cycling HSCs (Beerman I et al, 2014).
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Our study shows that mutation in FA genes results in hyperactive TGF-β signaling. This result suggests that the FA pathway normally functions to activate FANCD2 and to repress transcription of SMAD genes. We show that FANCD2, a critical downstream component of the FA pathway, binds to the promoter region of SMAD1. Activated FANCD2 has been previously reported to decrease transcription of the TNFα gene and to increase transcription of the TAp63 gene (Matsushita et al., 2011; Park et al., 2013). Our results indicate that hyperactive TGF-β pathway in FA cells contributes to the impairment of DNA repair due to downregulation of HR activity. The TGF-β pathway is known to play a role in DNA damage response (Barcellos-Hoff and Cucinotta, 2014). For instance, BRCA2 and SMAD3 form a complex and synergize in regulation of gene transcription (Preobrazhenska et al., 2002). SMAD3 also counteracts BRCA1-dependent repair of DNA double-strand breaks in human breast epithelial cells (Dubrovska et al., 2005). In addition, TGF-β pathway induces HR defects in breast cancer cells by regulating BRCA1, ATM, and MSH2 DNA repair genes (Liu et al., 2014). Moreover, TGF-β pathway activation promotes genomic instability by downregulating RAD51 protein expression in lung epithelial cells (Kanamoto et al., 2002). These studies further support our finding that inhibition of the hyperactive TGF-β pathway restores HR in FA HSPCs and improves their function. It remains to be determined whether the SMAD factors directly suppress HR gene transcription and promote NHEJ gene transcription. Our results elucidate a mechanism that contributes to bone marrow failure in FA patients– namely, the increased TGF-β signaling in FA HSPCs. TGF-β is a myelosuppressive cytokine that has been also implicated in the hematopoietic suppression of other hematopoietic diseases, including myelodysplastic syndrome (MDS), suggesting a more general
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mechanism of BMF (Suragani et al., 2014; Zhou et al., 2011; Zingariello et al., 2013). Plasma levels of TGF-β are mildly upregulated in MDS patients, and increased TGF-β immunohistochemical staining is evident in the bone marrow. Inhibition of TGF-β pathway after chemotherapy accelerates hematopoietic reconstitution by delaying the return of cycling HSCs to quiescence (Brenet et al., 2013). Murine and human FA HSPC function was enhanced after TGF-β pathway inhibition, consistent with the notion that TGF-β regulates quiescence and self-renewal of HSPCs (Bank and Kalrsson, 2014).
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Finally, our findings have implications for the clinical care of FA patients. Pharmacological agents targeting the TGF-β pathway have been developed for a variety of disease conditions, and some have shown efficacy in preclinical murine models and in human phase I and II clinical trials (Akhurst and Hata, 2012; Grafe et al., 2014; Suragani et al., 2014). Pharmacological inhibition of the TGF-β pathway appears to be safe and well tolerated, and 1D11 treatment does not cause obvious negative effects on general health, behavior, or growth in mice (Grafe et al., 2014). Inhibition of the TGF-β pathway may also be a clinically useful strategy during gene therapy for ex vivo expansion of rare HSPCs derived from FA patients (Rio et al., 2014). Additionally, the ability of TGF-β pathway inhibition to increase HR and decrease NHEJ may also provide a tool to improve CRISPR-mediated genome editing and may also be a mechanistic basis for the reduction of tumorigenesis.
EXPERIMENTAL PROCEDURES Detailed procedures can be found in the Supplemental Experimental Procedures. Genome-wide shRNA Screen
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The screen was performed using the Hannon-Elledge whole genome pooled shRNA library as previously described (Luo et al., 2009). Mice
Fancd2−/− mice in C57BL/6J background are previously described (Parmar et al., 2010). B6.SJL-PtprcaPep3b/BoyJ (Congenic B6, CD45.1+) mice and NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ (NSG) mice were purchased from The Jackson Laboratory. All experimental procedures were approved by the Animal Care and Use Committee of the Dana Farber Cancer Institute. Hematopoietic Stem/progenitor Cell Culture And Flow Cytometry Analysis
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The procedures of enrichment and cell staining for isolating HSPCs (Lin−cKit+Sca-1+) and HSCs (Lin−cKit+Sca-1+CD48−CD150+) from mouse bone marrow were performed as described (Zhang et al., 2012). Murine Bone Marrow Transplantation Donor cells (CD45.2+) were transplanted into lethally irradiated (10 Gy dose) recipient (congenic B6-CD45.1+ mice) along with 1×105cells competitive bone marrow cells from congenic B6-CD45.1+ mice. Peripheral blood from recipient mice was analyzed for donor cell engraftment as described (Parmar et al., 2010).
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Colony-forming Unit-spleen (CFU-S) Assay
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Recipient mice (wild-type, 8–12 weeks old) were irradiated with a split dose of 1100 rad (550 rad each, 4 hours apart) before transplantation. Forty thousand bone marrow cells from donor mice were transplanted into each recipient mouse. Ten to 12 days post-transplantation, spleens were harvested and fixed with Bouin fixative solution. In Vivo Xenograft Assay
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Human cord blood derived CD34+ cells were transduced with lentivirus encoding shFANCD2 or shControl as described (Ceccaldi et al., 2012). While cells were selected with 2μg/mL puromycin, cells were also treated with 10μg/mL GC1008. After 48h treatment, 2×105 cells were transplanted into sub-lethally irradiated (2.5Gy) NSG mice. The recipient mice were treated with 10mg/kg GC1008 at 3 doses per week for two weeks. Two and eight weeks after transplantation, human cells in peripheral blood (PB) were analyzed using antihuman CD45 antibody (eBioscience, 17–0459–42) by flow cytometry. Statistics Two-tailed P values for statistical analysis were obtained using Student’s t-test.
Supplementary Material Refer to Web version on PubMed Central for supplementary material.
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We are grateful to Raphael Ceccaldi and members of our laboratory for helpful discussion. We thank Benjamin Primack for maintaining Fancd2 mouse colony. We thank Dr. H. Lin (Massachusetts General Hospital), who generously provided the TGF-β reporter CAGA-Luciferase plasmid. We thank Genzyme Corp for providing the 1D11 and GC1008 antibodies. We thank the FA patients and their families. H.Z is supported by the Leukemia & Lymphoma Society Fellow Award. This work was also supported by grants from U.S. National Institutes of Health R01DK43889, R37HL052725 (to A.D.), and P01HL048546 (to M.G.).
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Figure 1. TGF-β Pathway Disruption Enhances Human FA Cellular Growth under Genotoxic Stress
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(A) RIGER P value analysis to identify top candidate genes in genome-wide screen. Top candidates are highlighted with different colors. Genes of the TGF-β pathway (BMP2, SMAD3, PDCD4) are pointed out by arrow. Genes involved in MMC metabolism (NQO1 and NFE2L2) are pointed out by arrowhead. (B) Clonogenic survival of GM6914 (FA-A fibroblasts) and FANCA-corrected GM6914 cells after shRNA mediated knockdown of SMAD3. Cells were exposed MMC and cell survival was determined after 10–12 days in culture. The average of two independent experiments is presented. Immunoblot in the right panel shows SMAD3 knockdown efficiency in GM6914 cells. (C,D) MMC sensitivity of EUFA316 (FA-G lymphoblasts) and FANCG-corrected EUFA316 cells incubated with or without 10μM SMAD3 inhibitor SIS3 or 10μM TGF-β inhibitor SD208. Cells were cultured in triplicates in presence of MMC and DMS0 or inhibitor for 5– 6 days and survival was determined. Data are representative of 3 independent experiments. (E) Acetaldehyde sensitivity of EUFA316 and FANCG-corrected EUFA316 cells incubated with or without 10μM SD208. Cells were exposed to acetaldehyde for 3 hours and survival
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was determined after culturing them for 5–6 days in presence of DMSO or SD208 in triplicates. The data are representative of 3 independent experiments. (F) Acetaldehyde sensitivity of EUFA316 cells after shRNA mediated knockdown SMAD3 and TP53. Right panel shows the immunoblots of the lysates from EUFA316 cells showing shRNA-mediated knockdown of SMAD3 or p53. Error bars represent mean ± s.e.m. *, p
