Thompson C B
Prog Clin Biol Res. 1986;215:361-71.
While the production of a subcellular particle that can be used as a basic building block for clot formation may be a significant adaptive advantage for mammals, little is known about the exact process by which platelets are produced. Studies of platelet heterogeneity suggest that platelet production is regulated to maintain a constant platelet mass. The number of platelets produced in a given interval is determined primarily by the number of cells differentiating along the megakaryocytic pathway and changes in the rate at which platelets are produced take several days to occur. In contrast, the mean platelet volume (MPV) appears to be determined by the conditions under which the platelets are produced and can be increased within hours of a change in platelet demand. This latter observation, coupled with the observation that megakaryocytes are active, motile cells responsive to a variety of humoral agonists suggests that platelet production is a dynamic process which is under tight regulatory control. Various issues of platelet production are considered in relationship to these observations. An approach to establishing a test model for platelet release is discussed.
虽然产生一种可作为血栓形成基本构建块的亚细胞颗粒对哺乳动物来说可能是一个重大的适应性优势,但对于血小板产生的确切过程却知之甚少。对血小板异质性的研究表明,血小板的产生受到调节以维持恒定的血小板数量。在给定时间段内产生的血小板数量主要由沿巨核细胞途径分化的细胞数量决定,并且血小板产生速率的变化需要几天时间才能发生。相比之下,平均血小板体积(MPV)似乎由血小板产生的条件决定,并且在血小板需求发生变化后的数小时内就可以增加。后一观察结果,再加上巨核细胞是对多种体液激动剂有反应的活跃、可移动细胞这一观察结果,表明血小板的产生是一个受到严格调控的动态过程。结合这些观察结果,对血小板产生的各种问题进行了探讨。讨论了建立血小板释放测试模型的方法。