巨核细胞向血小板的进化

MD, PhD Paquita Nurden (Haematologist), Christel Poujol (Research Assistant), PhD Alan T. Nurden (Reseach Director)
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引用次数: 28

摘要

巨核细胞是由多能干细胞经过细胞分裂、内复制和成熟的过程而产生的。逐渐地,MK细胞质被划分膜系统侵入,该系统被推测用于划分预先形成的血小板。一种理论认为,整个mk(或片段)进入血液后,它们在肺循环中物理分解成血小板。第二个理论是mk产生串珠状过程(原血小板),然后分离成血小板。功能重要的血小板受体,如GPIIb-IIIa和GPIb-IX复合物是MK谱系的特异性标记物。CD34和CD4存在于祖细胞中,但随着mk的成熟逐渐消失。基质细胞分泌细胞因子,产生细胞外基质蛋白,介导细胞接触相互作用,调节MK发育。血小板生成素的研究和转基因小鼠模型的使用有助于阐明MK生物学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
1 The evolution of megakaryocytes to platelets

Megakaryocytes (MKs) arise from pluripotent stem cells by a process of cell division, endoreplication and maturation. Progressively, the MK cytoplasm is invaded by the demarcation membrane system speculated to delimit pre-formed platelets. One theory is that the passage of entire MKs (or fragments) into the blood stream is followed by their physical break-up into platelets in the pulmonary circulation. A second theory is that MKs produce beaded processes (proplatelets) which then separate into platelets. Functionally vital platelet receptors such as GPIIb-IIIa and GPIb-IX complexes are specific markers of the MK lineage. CD34 and CD4 are present in progenitors but progressively disappear as MKs mature. Stroma cells secrete cytokines, produce extracellular matrix proteins and mediate cellular contact interactions that regulate MK development. Studies on thrombopoietin and the use of transgenic mouse models are helping to clarify MK biology.

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