Fawcett J, Buckley C, Holness C L, Bird I N, Spragg J H, Saunders J, Harris A, Simmons D L
Cell Adhesion Laboratory, Imperial Cancer Research Fund, John Radcliffe Hospital, Headington, Oxford, United Kingdom.
J Cell Biol. 1995 Mar;128(6):1229-41. doi: 10.1083/jcb.128.6.1229.
CD31 is a member of the immunoglobulin superfamily consisting of six Ig-related domains. It is constitutively expressed by platelets, monocytes, and some lymphocytes, but at tenfold higher levels on vascular endothelial cells. CD31 has both homotypic and heterotypic adhesive properties. We have mapped the homotypic binding sites using a deletion series of CD31-Fc chimeras and a panel of anti-CD31 monoclonal antibodies. An extensive surface of CD31 is involved in homotypic binding with domains 2 and 3 and domains 5 and 6 playing key roles. A model consistent with the experimental data is that CD31 on one cell binds to CD31 on an apposing cell in an antiparallel interdigitating mode requiring full alignment of the six domains of each molecule. In addition to establishing intercellular homotypic contacts. CD31 binding leads to augmented adhesion via beta 1 integrins. The positive cooperation between CD31 and beta 1 integrins can occur in heterologous primate cells (COS cells). The interaction is specific to both CD31 and beta 1 integrins. Neither intercellular adhesion molecule-1 (ICAM-1)/leukocyte function-associated antigen-1 (LCAM-1) nor neural cell adhesion molecule (NCAM)/NCAM adhesion leads to recruitment of beta 1 integrin adhesion pathways. Establishment of CD31 contacts have effects on the growth and morphology of endothelial cells. CD31(D1-D6)Fc inhibits the growth of endothelial cells in culture. In addition, papain fragments of anti-CD31 antibodies (Fab fragments) disrupt interendothelial contact formation and monolayer integrity when intercellular contacts are being formed. The same reagents are without effect once these contacts have been established, suggesting that CD31-CD31 interactions are critically important only in the initial phases of intercellular adhesion.
CD31是免疫球蛋白超家族的成员,由六个免疫球蛋白相关结构域组成。它在血小板、单核细胞和一些淋巴细胞中组成性表达,但在血管内皮细胞上的表达水平要高十倍。CD31具有同型和异型黏附特性。我们使用一系列CD31-Fc嵌合体缺失突变体和一组抗CD31单克隆抗体绘制了同型结合位点图谱。CD31的一个广泛表面参与同型结合,其中结构域2和3以及结构域5和6起关键作用。与实验数据一致的模型是,一个细胞上的CD31以反平行相互交错模式与相邻细胞上的CD31结合,这需要每个分子的六个结构域完全对齐。除了建立细胞间同型接触外,CD31结合还通过β1整合素增强黏附。CD31与β1整合素之间的正向协同作用可发生在异源灵长类细胞(COS细胞)中。这种相互作用对CD31和β1整合素均具有特异性。细胞间黏附分子-1(ICAM-1)/白细胞功能相关抗原-1(LCAM-1)或神经细胞黏附分子(NCAM)/NCAM黏附均不会导致β1整合素黏附途径的募集。CD31接触的建立对内皮细胞的生长和形态有影响。CD31(D1-D6)Fc抑制培养的内皮细胞生长。此外,在细胞间接触形成时,抗CD31抗体的木瓜蛋白酶片段(Fab片段)会破坏内皮细胞间接触的形成和单层完整性。一旦这些接触建立,相同的试剂则没有作用,这表明CD31-CD31相互作用仅在细胞间黏附的初始阶段至关重要。