Odell T T, Murphy J R, Jackson C W
Blood. 1976 Nov;48(5):765-75.
Rats were made acutely thrombocytopenic by injection of antiplatelet serum. Marrow sections and squash preparations were made at intervals during 120 hr. Determinations were made of mitotic index, stage of maturation, ploidy level, and cell size of megakaryocytes; number and size of platelets were measured. Increased endomitosis among megakaryocytes was followed by an increase in the proportion of immature megakaryocytes, a greater average ploidy level of recognized megakaryocytes, and larger megakaryocytes. Maximum changes in these several parameters occurred between 32 and 72 hr after induction of thrombocytopenia. By 120 hr all megakarocyte parameters were near normal. For about 3 days, beginning at about 36 hr, platelet numbers increased rapidly. Average platelet size rose and returned to normal within about 60 hr. Changes in ploidy and size of megakaryocytes were measured in the immature and mature maturation stages. The results suggest that the initial stimulus in response to acute thrombocytopenia acts primarily on diploid precursors, programming them to mature into a population of megakaryocytes with an average ploidy approximately one level greater than in normal rats and a proportionate increase in cell size. The larger megakaryocytes presumably produce more platelets, accounting for a major part of the increased rate of platelet production. Since the changes in megakaryocytes begin to reverse before circulating platelet numbers have reached the normal level, reversal of the stimulus appears to be initiated by some change other than platelet mass.
通过注射抗血小板血清使大鼠急性血小板减少。在120小时内每隔一段时间制作骨髓切片和压片标本。测定巨核细胞的有丝分裂指数、成熟阶段、倍性水平和细胞大小;测量血小板的数量和大小。巨核细胞内复制增加后,未成熟巨核细胞的比例增加,已识别的巨核细胞平均倍性水平更高,且巨核细胞更大。这些参数的最大变化发生在血小板减少诱导后的32至72小时之间。到120小时时,所有巨核细胞参数接近正常。从大约36小时开始,血小板数量在大约3天内迅速增加。平均血小板大小上升,并在大约60小时内恢复正常。在未成熟和成熟阶段测量巨核细胞的倍性和大小变化。结果表明,对急性血小板减少的初始刺激主要作用于二倍体前体细胞,使其编程成熟为一群巨核细胞,其平均倍性比正常大鼠高约一个水平,细胞大小相应增加。较大的巨核细胞可能产生更多的血小板,这是血小板生成率增加的主要原因。由于巨核细胞的变化在循环血小板数量达到正常水平之前就开始逆转,刺激的逆转似乎是由血小板数量以外的其他变化引发的。