Byzova T V, Romanov Iu A, Blasik T N, Mazurov A V
Biokhimiia. 1995 Aug;60(8):1292-301.
Monoclonal antibody (MAb) CRC81 against P-selectin, a membrane cell adhesion protein of platelets and endothelial cells (EC), has been obtained and characterized. The antibody selectively interacted with the surface of activated platelets and EC due to the redistribution of P-selectin from intracellular organelles onto the surface by activation. MAb CRC81 could recognize not only human but also rabbit and dog P-selectins. MAb CRC81 was used to establish the heterogeneity of human aorta EC with regard to the P-selectin content. Some of the cells in culture did not contain this protein but were nevertheless positively stained for von Willebrand factor, a specific marker for EC which, similar to P-selectin, is localized in Weibel-Palade's bodies. The proportion of P-selectin negative EC increased dramatically in the course of cell passaging: in primary cultures of aortic EC their content was about 15%, while after the 6th passage it exceeded 90%.
已获得并鉴定出一种针对P-选择素的单克隆抗体(MAb)CRC81,P-选择素是血小板和内皮细胞(EC)的一种膜细胞粘附蛋白。由于激活作用使P-选择素从细胞内细胞器重新分布到表面,该抗体与活化血小板和内皮细胞表面发生选择性相互作用。MAb CRC81不仅可以识别人类的P-选择素,还能识别兔和犬的P-选择素。利用MAb CRC81确定了人主动脉内皮细胞在P-选择素含量方面的异质性。培养中的一些细胞不含这种蛋白,但对血管性血友病因子呈阳性染色,血管性血友病因子是内皮细胞的一种特异性标志物,与P-选择素类似,定位于魏尔-帕拉德小体中。在细胞传代过程中,P-选择素阴性内皮细胞的比例急剧增加:在主动脉内皮细胞的原代培养中,其含量约为15%,而在第6代传代后超过90%。