Wistar Furth大鼠巨核细胞缺乏密集的室室和细胞间斑块,即富含细胞骨架蛋白的膜状结构。

P E Stenberg, J H Beckstead, C W Jackson
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引用次数: 3

摘要

Wistar Furth (WF)大鼠的血小板生成表型异常,巨核细胞形态异常,血小板体积大于正常,血小板α颗粒蛋白缺乏。在5-氟尿嘧啶给药后,在刺激巨核细胞生成过程中,将WF大鼠巨核细胞与血小板形成正常的大鼠(Wistar)进行超微结构比较,发现了正常大鼠巨核细胞中先前未被识别的膜结构,以及WF巨核细胞中另外两种异常。这种新结构是相邻正常巨核细胞相对质膜细胞质表面的电子密度区。这些改良的局灶黏附型接触间隔分布在相邻的巨核细胞之间,并被细胞外物质的沉积隔开。这些结构也存在于未受干扰的Wistar大鼠骨髓中巨核细胞的相对质膜之间,但在WF大鼠的巨核细胞之间不存在。第二个WF大鼠巨核细胞异常是缺乏细胞质致密室,这是另一个与巨核细胞划分膜系统连续的特化膜结构。超微结构免疫金标记显示,Wistar大鼠巨核细胞的细胞间斑块和致密室均富含细胞骨架蛋白,包括肌动蛋白、α -肌动蛋白、talin和vinculin。我们假设细胞骨架蛋白功能的异常可能是导致WF大鼠缺乏这些结构的原因。
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Wistar Furth rat megakaryocytes lack dense compartments and intercellular plaques, membranous structures rich in cytoskeletal proteins.

Wistar Furth (WF) rats have an abnormal thrombopoietic phenotype with morphologically aberrant megakaryocytes, larger than normal mean platelet volume, and platelet alpha-granule protein deficiency. Here, ultrastructural comparisons of WF rat megakaryocytes to those of rats (Wistar) with normal platelet formation during stimulated megakaryocytopoiesis following 5-fluorouracil administration, have revealed a previously unrecognized membrane structure in normal rat megakaryocytes, and two additional abnormalities in WF megakaryocytes. The novel structures were zones of electron density on the cytoplasmic face of apposed plasma membranes of adjoining normal megakaryocytes. These modified focal adhesion-type contacts were distributed at intervals between adjacent megakaryocytes, and were spaced by deposits of extracellular material. These structures also were present between apposed plasma membranes of Wistar rat megakaryocytes in unperturbed marrows, but were absent between megakaryocytes of WF rats. The second WF rat megakaryocyte abnormality is the absence of cytoplasmic dense compartments, another specialized membranous structure that is continuous with the megakaryocyte demarcation membrane system. Both the intercellular plaques and dense compartments of Wistar rat megakaryocytes were found to be rich in cytoskeletal proteins including actin, alpha-actinin, talin, and vinculin as indicated by ultrastructural immunogold labeling. We hypothesize that an abnormality in cytoskeletal protein function may be responsible for the lack of these structures in the WF rat.

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