Muller W A, Weigl S A, Deng X, Phillips D M
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, New York.
J Exp Med. 1993 Aug 1;178(2):449-60. doi: 10.1084/jem.178.2.449.
Platelet/endothelial cell adhesion molecule 1 (PECAM-1; CD31) is crucial to the process of leukocyte transmigration through intercellular junctions of vascular endothelial cells. A monoclonal antibody to PECAM, or recombinant soluble PECAM, blocks transendothelial migration of monocytes by 70-90%. Pretreating either the monocytes or the endothelial junctions with antibody blocks transmigration. If the endothelium is first activated by cytokines, anti-PECAM antibody or soluble recombinant PECAM again block transmigration of both monocytes and neutrophils. Anti-PECAM does not block chemotaxis of either cell type. Light and electron microscopy reveal that leukocytes blocked in transmigration remain tightly bound to the apical surface of the endothelial cell, precisely over the intercellular junction. Thus, the process of leukocyte emigration can be dissected into three successive stages: rolling, mediated by the selectin class of adhesion molecules; tight adhesion, mediated by the leukocyte integrins and their endothelial cell counter-receptors; and now transmigration, which, based on these studies, requires PECAM-1.
血小板/内皮细胞黏附分子1(PECAM-1;CD31)对于白细胞通过血管内皮细胞间连接进行迁移的过程至关重要。一种针对PECAM的单克隆抗体或重组可溶性PECAM可使单核细胞的跨内皮迁移减少70%至90%。用抗体预处理单核细胞或内皮连接均可阻断迁移。如果内皮细胞首先被细胞因子激活,抗PECAM抗体或可溶性重组PECAM会再次阻断单核细胞和中性粒细胞的迁移。抗PECAM并不阻断这两种细胞类型的趋化作用。光学显微镜和电子显微镜显示,迁移受阻的白细胞仍紧密结合在内皮细胞的顶端表面,恰好位于细胞间连接处上方。因此,白细胞渗出过程可分为三个连续阶段:由选择素类黏附分子介导的滚动;由白细胞整合素及其内皮细胞反受体介导的紧密黏附;以及基于这些研究表明需要PECAM-1的跨内皮迁移。