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Downregulation of GATA1 drives impaired hematopoiesis in primary myelofibrosis

机译:GATA1的下调驱动原发性骨髓纤维化造血功能受损。

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Primary myelofibrosis (PMF) is a clonal hematologic malignancy characterized by BM fibrosis, extramedullary hematopoiesis, circulating CD34+ cells, splenomegaly, and a propensity to evolve to acute myeloid leukemia. Moreover, the spleen and BM of patients harbor atypical, clustered megakaryocytes, which contribute to the disease by secreting profibrotic cytokines. Here, we have revealed that megakaryocytes in PMF show impaired maturation that is associated with reduced GATA1 protein. In investigating the cause of GATA1 downregulation, our gene-expression study revealed the presence of the RPS14-deficient gene signature, which is associated with defective ribosomal protein function and linked to the erythroid lineage in 5q deletion myelodysplastic syndrome. Surprisingly, reduced GATA1 expression and impaired differentiation were limited to megakaryocytes, consistent with a proproliferative effect of a GATA1 deficiency on this lineage. Importantly, expression of GATA1 effectively rescued maturation of PMF megakaryocytes. Together, these results suggest that ribosomal deficiency contributes to impaired megakaryopoiesis in myeloproliferative neoplasms.
机译:原发性骨髓纤维化(PMF)是一种以BM纤维化,髓外造血,循环CD34 +细胞,脾肿大和发展为急性髓系白血病为特征的克隆性血液恶性肿瘤。此外,患者的脾脏和BM带有非典型的簇状巨核细胞,它们通过分泌纤维化细胞因子而导致疾病。在这里,我们发现PMF中的巨核细胞显示出与减少的GATA1蛋白有关的受损的成熟。在调查GATA1下调的原因时,我们的基因表达研究揭示了RPS14缺陷基因签名的存在,其与核糖体蛋白功能缺陷有关,并与5q缺失骨髓增生异常综合征中的红系谱系有关。出人意料的是,减少的GATA1表达和分化受损仅限于巨核细胞,这与GATA1缺乏对该谱系的增生作用一致。重要的是,GATA1的表达有效挽救了PMF巨核细胞的成熟。在一起,这些结果表明核糖体缺乏症导致骨髓增生性肿瘤巨核细胞生成受损。

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