Leĭtin V L, Misse'lvits F, Liubimova E V, Domogatskiĭ S P
Kardiologiia. 1989 Sep;29(9):74-7.
Scanning electron microscopy was used to examine the interaction of platelets with types I, III, IV, and V human collagens (CI, CIII, CIV, and CV substrates) immobilized on the surface of cultural plates. Basic differences were found in the activity of collagen substrates against platelets. On the CV substrate, virtually all the adhesive platelets were in a non-spreading++ state, i.e. at the stage of initial attachment to the spread. The CIV substrate showed initial attachment, spreading, and attachment of platelets from the suspension to the spread platelets. In addition to the processes occurring at the CIV substrate, the CI and CIII substrates produced multilayer platelet aggregates on the strata of spreading platelets (thromboid aggregates). The surfaces covered with various types of collagens are an adequate model for quantitative step-by-step study of the formation of parietal thrombocytic thrombi and of mechanisms of this process control.
利用扫描电子显微镜检查血小板与固定在培养板表面的I型、III型、IV型和V型人胶原蛋白(CI、CIII、CIV和CV底物)之间的相互作用。发现胶原蛋白底物对血小板的活性存在基本差异。在CV底物上,几乎所有黏附的血小板都处于非铺展状态,即在最初附着到铺展阶段。CIV底物显示血小板从悬浮液到铺展血小板的初始附着、铺展和附着。除了在CIV底物上发生的过程外,CI和CIII底物在铺展血小板层上产生多层血小板聚集体(血栓样聚集体)。覆盖有各种类型胶原蛋白的表面是对壁血小板血栓形成过程及其控制机制进行定量逐步研究的合适模型。