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赤芽球の分化·成熟

机译:红细胞的分化和成熟

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Erythropoietin/receptor (EPO/EPOR) system is a pivotal regulator of erythropoiesis. Indeed, EPO-deficient and EPOR-deficient mice are embryonic lethal. The EPOR has two dominant forms, a full-length one (EPOR-F) and a truncated one (EPOR-T), by an alternative splicing mechanism of mRNA The EPOR-T expresses abundantly in more immature erythroid progenitor cells. The EPOR-T acts as a dominant negative regulator of EPO-signals for proliferation and anti-apoptosis in cell lines. Presumably, the EPOR-T forms a heterodimer with EPOR-F and results in inhibition of efficient EPO-signals. Transgenic mice over-expressing the EPOR-T show an anemia and a severe defect in recovery from acute anemia. This result strongly suggests that the EPOR-T acts as a negative regulator for erythropoiesis also in vivo. It was reported that a large number of erythroid precursor cells die of apoptosis under physiological concentration of EPO in mouse. At higher EPO-concentration, these erythroid precursors escape from apoptosis and mature into erythrocytes. This mechanism might allow immediate supply of a large number of eryth-rocytes in case of acute anemia. In such mechanism, the EPOR-T might play an important role as a regulator of EPO-induced signals in erythroid cells.
机译:促红细胞生成素/受体(EPO / EPOR)系统是促红细胞生成的关键调节剂。实际上,EPO缺陷和EPOR缺陷的小鼠是胚胎致死的。 EPOR具有两种主要形式,全长形式(EPOR-F)和截短形式(EPOR-T),这是通过mRNA的另一种剪接机制实现的。EPOR-T在较不成熟的红系祖细胞中大量表达。 EPOR-T充当EPO信号在细胞系中的增殖和抗凋亡的主要负调节剂。据推测,EPOR-T与EPOR-F形成异二聚体并导致有效EPO信号的抑制。过表达EPOR-T的转基因小鼠表现出贫血和急性贫血恢复中的严重缺陷。该结果强烈表明,EPOR-T在体内也充当促红细胞生成的负调节剂。据报道,在小鼠体内生理浓度的EPO下,大量的类红细胞前体细胞因凋亡而死亡。在较高的EPO浓度下,这些类红细胞前体从凋亡中逃脱,并成熟为红细胞。这种机制可能在急性贫血的情况下允许立即供应大量的红血球细胞。在这种机制中,EPOR-T作为红细胞中EPO诱导信号的调节剂可能发挥重要作用。

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