Hession C, Moy P, Tizard R, Chisholm P, Williams C, Wysk M, Burkly L, Miyake K, Kincade P, Lobb R
Biogen, Inc., 14 Cambridge Center, MA 02142.
Biochem Biophys Res Commun. 1992 Feb 28;183(1):163-9. doi: 10.1016/0006-291x(92)91623-x.
Vascular cell adhesion molecule-1 (VCAM1) is a member of the immunoglobulin (Ig) superfamily which interacts with the integrin very late antigen 4 (VLA4). We have cloned the cDNAs for both murine and rat VCAM1 from endotoxin-treated lung libraries. Both sequences encode proteins with seven extracellular Ig-like domains, which show 75.9% and 76.9% identity, respectively, with human VCAM1. Both murine and human cell lines show VLA4-dependent binding to COS cells transiently expressing murine and rat VCAM1. Two mAbs, M-K/1 and M-K/2, which recognize an antigen on murine bone marrow stromal cell lines, bind to murine VCAM1 expressed in COS cells and block VCAM1-dependent adhesion, confirming that these mAbs recognize murine VCAM1.
血管细胞黏附分子-1(VCAM1)是免疫球蛋白(Ig)超家族的成员,它与整合素极晚期抗原4(VLA4)相互作用。我们从内毒素处理的肺文库中克隆了小鼠和大鼠VCAM1的cDNA。这两个序列编码的蛋白质都有七个细胞外免疫球蛋白样结构域,分别与人VCAM1有75.9%和76.9%的同源性。小鼠和人细胞系都显示出VLA4依赖性地与瞬时表达小鼠和大鼠VCAM1的COS细胞结合。两种单克隆抗体M-K/1和M-K/2可识别小鼠骨髓基质细胞系上的一种抗原,它们与COS细胞中表达的小鼠VCAM1结合并阻断VCAM1依赖性黏附,证实这些单克隆抗体识别小鼠VCAM1。