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血小板生成素对人类晚期红细胞生成具有分化作用。

Thrombopoietin has a differentiative effect on late-stage human erythropoiesis.

作者信息

Liu W, Wang M, Tang D C, Ding I, Rodgers G P

机构信息

Molecular and Clinical Hematology Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Br J Haematol. 1999 May;105(2):459-69.

Abstract

To further explore the mechanism of the effect of thrombopoietin (TPO) on erythropoiesis, we used a two-phase culture system to investigate the effect of TPO on late-stage human erythroid lineage differentiation. In serum-free suspension and semisolid cultures of human peripheral blood derived erythroid progenitors, TPO alone did not produce benzidine-positive cells. However, in serum-containing culture, TPO alone stimulated erythroid cell proliferation and differentiation, demonstrated by erythroid colony formation, production of benzidine-positive cells and haemoglobin (Hb) synthesis. Monoclonal anti-human erythropoietin antibody and anti-human erythropoietin receptor antibody completely abrogated the erythroid differentiative ability of TPO in the serum-containing systems. This implied that binding of EPO and EPO-R was essential for erythropoiesis and the resultant signal transduction may be augmented by the signals emanating from TPO-c-Mpl interaction. Experiment of withdrawal of TPO further demonstrated the involvement of TPO in late-stage erythropoiesis. RT-PCR results showed that there was EPO-R but not c-Mpl expression on developing erythroblasts induced by TPO in serum-containing system. Our results establish that TPO affects not only the proliferation of erythroid progenitors but also the differentiation of erythroid progenitors to mature erythroid cells.

摘要

为进一步探究血小板生成素(TPO)对红细胞生成作用的机制,我们采用两阶段培养系统来研究TPO对晚期人类红系谱系分化的影响。在人外周血来源的红系祖细胞的无血清悬浮培养和半固体培养中,单独使用TPO不会产生联苯胺阳性细胞。然而,在含血清培养中,单独使用TPO可刺激红系细胞增殖和分化,这通过红系集落形成、联苯胺阳性细胞的产生及血红蛋白(Hb)合成得以证明。单克隆抗人促红细胞生成素抗体和抗人促红细胞生成素受体抗体完全消除了含血清体系中TPO的红系分化能力。这表明促红细胞生成素(EPO)与促红细胞生成素受体(EPO-R)的结合对红细胞生成至关重要,并且由TPO-c-Mpl相互作用产生的信号可能增强了由此产生的信号转导。去除TPO的实验进一步证明了TPO参与晚期红细胞生成。逆转录聚合酶链反应(RT-PCR)结果显示,在含血清体系中由TPO诱导的发育中的成红细胞上有EPO-R表达,但没有c-Mpl表达。我们的结果表明,TPO不仅影响红系祖细胞的增殖,还影响红系祖细胞向成熟红细胞的分化。

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