Hegyi E, Heilbrun L K, Nakeff A
II Department of Medicine, Medical University of Szeged, Hungary.
Exp Hematol. 1990 Aug;18(7):789-93.
Different ploidy classes of rat megakaryocytes were sorted by flow cytometry from highly purified perfusion-fixed megakaryocyte cell suspensions prepared by sequential centrifugal elutriation and Percoll gradient centrifugation. Sorted cell populations were studied for the localization of platelet factor 4 (PF-4) probed with the monoclonal antibody 2E7 in order to clarify the relevance of PF-4 localization to the cytoplasmic and nuclear development of megakaryocytes. The relative numbers of labeled alpha granules and labeled alpha granule-related small vesicular structures (AGR-SVS) were quantitated using the gold-labeled antibody detection method and correlated with DNA content and cytoplasmic maturation in individual megakaryocytes. We determined that the stage of cytoplasmic maturation exerted a significant effect on the proportion of labeled alpha granules and labeled AGR-SVS. A significant interaction effect of stage and ploidy class resulted in the stage effect on proportion of labeled alpha granules being significant only in two of the three ploidy classes. The least mature cells present within each ploidy group exhibited PF-4 labeling mostly in SVS that were not related to alpha granules. During subsequent cytoplasmic maturation, more of the labeled SVS were seen related to alpha granules, with more of the mature alpha granules themselves becoming labeled. Polyploidization also affected the proportion of labeled AGR-SVS. Our data suggest that SVS play a role in the intramegakaryocytic transport of PF-4 into alpha granules. These data provide evidence of the complexity of megakaryocytic differentiation involving both cytoplasmic maturation and nuclear endoreduplication as reflected in PF-4 expression.
通过连续离心淘析和Percoll梯度离心制备高度纯化的灌注固定巨核细胞悬液,利用流式细胞术对大鼠不同倍体类别的巨核细胞进行分选。为了阐明血小板因子4(PF-4)定位与巨核细胞胞质和核发育的相关性,使用单克隆抗体2E7对分选的细胞群体进行血小板因子4(PF-4)定位研究。使用金标抗体检测方法对标记的α颗粒和标记的α颗粒相关小泡结构(AGR-SVS)的相对数量进行定量,并与单个巨核细胞的DNA含量和胞质成熟度相关联。我们确定,胞质成熟阶段对标记的α颗粒和标记的AGR-SVS的比例有显著影响。阶段和倍体类别的显著交互作用导致阶段对标记的α颗粒比例的影响仅在三个倍体类别中的两个中显著。每个倍体组中最不成熟的细胞中,PF-4标记大多出现在与α颗粒无关的小泡结构中。在随后的胞质成熟过程中,更多与α颗粒相关的标记小泡结构出现,更多成熟的α颗粒本身也被标记。多倍体化也影响标记的AGR-SVS的比例。我们的数据表明,小泡结构在PF-4向α颗粒的巨核细胞内运输中起作用。这些数据提供了证据,证明巨核细胞分化的复杂性涉及胞质成熟和核内复制,这在PF-4表达中得到体现。