White J G, Clawson C C
Ultrastruct Pathol. 1980 Oct-Dec;1(4):533-58. doi: 10.3109/01913128009140561.
Advances in biochemistry, physiology, immunology, and cytochemistry, combined with a variety of new approaches for the evaluation of fine structure, have yielded new insights into the structural physiology and pathology of blood platelets. Subpopulations of platelet granules have been clearly defined; they include the catalase containing organelles referred to as peroxisomes; lysosomes enclosing hydrolytic enzymes; and the alpha-granules in which platelet factor 4, mitogenic factor, beta thromboglobulin, thrombin sensitive protein, fibrinogen, and coagulation factor V are localized. Features of platelet membrane systems have been particularly well-delineated, and recent evidence suggests that membrane complexes serve as the sarcoplasmic reticulum of platelets and the site of prostaglandin synthesis. Improved understanding of platelet biostructure resulting from these observations has made it possible to develop specific relationships between defects in structure and pathological behavior of the cells in vitro and in vivo.
生物化学、生理学、免疫学和细胞化学的进展,结合各种用于评估精细结构的新方法,为血小板的结构生理学和病理学带来了新的见解。血小板颗粒的亚群已被明确界定;它们包括含有过氧化氢酶的细胞器,即过氧化物酶体;包绕水解酶的溶酶体;以及α颗粒,血小板因子4、促有丝分裂因子、β-血小板球蛋白、凝血酶敏感蛋白、纤维蛋白原和凝血因子V定位于其中。血小板膜系统的特征已得到特别清晰的描述,最近的证据表明膜复合物充当血小板的肌浆网和前列腺素合成的场所。这些观察结果使人们对血小板生物结构有了更好的理解,从而有可能在体外和体内建立细胞结构缺陷与病理行为之间的特定关系。