Stenberg P E, Levin J
Department of Laboratory Medicine, University of California School of Medicine, San Francisco 94143.
J Cell Physiol. 1989 Oct;141(1):160-9. doi: 10.1002/jcp.1041410124.
Thrombopoiesis was studied in mice after the induction of acute immune thrombocytopenia with platelet antiserum (PAS). Utilizing electron microscopy, we examined platelets and megakaryocytes (MK) obtained 4, 8, 12, 24, 48, 72, and 120 hr after administration of PAS. Four to 24 hr after injection of PAS, the majority of bone marrow MK were normal in size and organelle distribution. The demarcation membrane system (DMS) extended normally throughout the mature cell cytoplasm at these times. However, approximately 50% of MK observed 48 hr and 72 hr after injection of PAS were significantly larger than normal, and often had demarcation membranes confined to an area between a peripheral organelle-deficient zone and a central nuclear zone. The median values for sectional areas of platelets obtained 8-72 hr after administration of PAS were significantly greater than the median value for sectional areas of platelets in a pooled control sample. The proportion of cytoplasm to surface-connected canalicular system appeared greater than normal in most large platelets from the PAS samples; and increased numbers of profiles of Golgi complex and endoplasmic reticulum were observed. By 48 hr post-injection of PAS (at which time the modal ploidy class of MK has shifted from 16N to 32N; Corash et al., Blood 70:177, 1987), most platelets were normal in size and cytoplasmic appearance. At 120 hr post-injection of PAS, virtually all platelets exhibited a normal size and complement of organelles, and MK also had returned to normal. Our data indicate that in response to acute thrombocytopenia, MK prematurely release platelets which differ from normal platelets in size and cytoplasmic appearance. There was a marked dissociation between alterations in platelets and MK, since a statistically significant increase in platelet sectional area occurred 40 hr before the shift in modal ploidy class of MK, and platelet size subsequently decreased toward normal during the period that has been shown to be associated with the maximum shift in MK ploidy. These results strongly suggest that the characteristics of platelet release do not depend on the ploidy or cytoplasmic characteristics of MK.
用血小板抗血清(PAS)诱导小鼠急性免疫性血小板减少症后,对其血小板生成进行了研究。利用电子显微镜,我们检查了在给予PAS后4、8、12、24、48、72和120小时获得的血小板和巨核细胞(MK)。注射PAS后4至24小时,大多数骨髓MK的大小和细胞器分布正常。此时,分界膜系统(DMS)正常延伸至整个成熟细胞的细胞质。然而,注射PAS后48小时和72小时观察到的约50%的MK明显大于正常,并且分界膜通常局限于外周细胞器缺乏区和中央核区之间的区域。给予PAS后8至72小时获得的血小板截面积的中位数显著大于合并对照样本中血小板截面积的中位数。在来自PAS样本的大多数大血小板中,细胞质与表面连接的小管系统的比例似乎大于正常;并且观察到高尔基体复合体和内质网的轮廓数量增加。注射PAS后48小时(此时MK的模态倍性类别已从16N转变为32N;Corash等人,《血液》70:177,1987),大多数血小板的大小和细胞质外观正常。注射PAS后120小时,几乎所有血小板的大小和细胞器组成均正常,MK也已恢复正常。我们的数据表明,对急性血小板减少症的反应中,MK过早释放的血小板在大小和细胞质外观上与正常血小板不同。血小板和MK的变化之间存在明显的分离,因为血小板截面积的统计学显著增加发生在MK模态倍性类别转变前40小时,并且在已显示与MK倍性最大转变相关的期间,血小板大小随后朝着正常方向降低。这些结果强烈表明,血小板释放的特征不取决于MK的倍性或细胞质特征。