Molecular Medicine Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Semin Hematol. 2010 Jul;47(3):227-34. doi: 10.1053/j.seminhematol.2010.03.006.
It is becoming increasingly clear that most mammalian cells are capable of undergoing apoptosis and that, within particular lineages, specific apoptotic pathways have evolved to regulate survival and turnover. The role of apoptosis in the megakaryocyte lineage is an intriguing one. Various insults, such as chemotherapeutics, autoantibodies, and human immunodeficiency virus (HIV), have been suggested to induce the apoptotic death of megakaryocytes and/or their progenitors. Conversely, apoptotic processes have been implicated in megakaryocyte development and platelet production. Platelets also contain functional apoptotic pathways, which circumscribe their survival. It has even been suggested that platelet activation responses involve components of the apoptotic machinery, highlighting a potential role for apoptotic processes in hemostasis and thrombosis. This review discusses the current state of knowledge about how apoptosis and apoptotic proteins contribute to the generation and function of megakaryocytes and platelets.
越来越明显的是,大多数哺乳动物细胞都能够发生细胞凋亡,并且在特定谱系中,已经进化出特定的凋亡途径来调节存活和更新。细胞凋亡在巨核细胞谱系中的作用是一个有趣的问题。各种刺激物,如化疗药物、自身抗体和人类免疫缺陷病毒 (HIV),已被认为可诱导巨核细胞及其前体细胞发生凋亡性死亡。相反,凋亡过程也与巨核细胞的发育和血小板的产生有关。血小板还含有功能凋亡途径,限制其存活。甚至有人提出,血小板激活反应涉及凋亡机制的组成部分,这突出了凋亡过程在止血和血栓形成中的潜在作用。本文综述了目前关于细胞凋亡和凋亡蛋白如何促进巨核细胞和血小板生成和功能的知识状态。