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Differentiation and cell density upregulate cytochrome c levels in megakaryoblastic cell lines: Implications for analysis of CYCS-associated thrombocytopenia

机译:分化和细胞密度上调巨核细胞细胞系中细胞色素c的水平:CYCS相关的血小板减少症分析的意义

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摘要

Mutations in the cytochrome c gene (CYCS) cause autosomal dominant thrombocytopenia by an unknown mechanism. While attempting to generate megakaryoblastic cell lines exogenously expressing cytochrome c variants, we discovered that endogenous cytochrome c expression increased both upon induction of differentiation with the phorbol ester phorbol 12-myristate 13-acetate (PMA), and as cell density increased. A concomitant increase in cytochrome c oxidase subunit II in response to PMA, but not cell higher cell density, suggests upregulation of the mitochondrial respiratory chain may be a specific feature of differentiation. These results highlight the likely importance of cytochrome c in both differentiating and proliferating cells, and illustrate the unsuitability of megakaryoblastic lines for modeling CYCS-associated thrombocytopenia.
机译:细胞色素c基因(CYCS)中的突变通过未知机制导致常染色体显性血小板减少症。在尝试生成外源性表达细胞色素c变体的巨核细胞细胞系时,我们发现内源性细胞色素c的表达在用佛波醇酯佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)诱导分化时都增加了,并且随着细胞密度的增加而增加。响应PMA的细胞色素C氧化酶亚基II的同时增加,而不是细胞较高的细胞密度,表明线粒体呼吸链的上调可能是分化的特定特征。这些结果突出了细胞色素c在分化和增殖细胞中的重要性,并说明巨核细胞系不适用于CYCS相关血小板减少症的建模。

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