Zucker W H, Mason R G
Am J Pathol. 1976 Jan;82(1):129-42.
Whole blood anticoagulated with EDTA was stirred with high concentrations of a microcrystalline bovine dermal collagen preparation in order to study the interactions of blood cells with collagen at the ultrastructural level. Blood from normal subjects and from patients congenitally deficient in Factors VIII or XII or with thrombasthenia or von Willebrands disease was used. In scanning and transmission electron microscopic studies with blood from normal subjects and patients, platelets were seen to adhere to collagen, develop cell surface undulations, form pseudopods, and undergo morphologic changes suggestive of the release reaction. Although thrombasthenic platelets adhered to collagen, pseudopods formed by these cells were remarkably angulated and nodular. Relatively few von Willebrands platelets adhered to collagen, but those platelets that did adhere underwent the usual sequence of morphologic changes.
用乙二胺四乙酸(EDTA)抗凝的全血与高浓度的微晶牛真皮胶原制剂搅拌,以在超微结构水平研究血细胞与胶原的相互作用。使用了来自正常受试者以及先天性缺乏因子VIII或XII、或患有血小板无力症或血管性血友病患者的血液。在对正常受试者和患者血液进行扫描和透射电子显微镜研究中,可见血小板粘附于胶原,细胞表面出现起伏,形成伪足,并发生提示释放反应的形态学变化。尽管血小板无力症患者的血小板粘附于胶原,但这些细胞形成的伪足明显呈角状且有结节。血管性血友病患者的血小板相对较少粘附于胶原,但那些确实粘附的血小板会经历通常的形态学变化序列。