Baumgartner Werner, Drenckhahn Detlev
Insitute of Anatomy and Cell Biology, Julius-Maximilians University of Würzburg, Koellikerstrasse 6, 97070 Würzburg, Germany.
Eur Biophys J. 2002 Dec;31(7):532-8. doi: 10.1007/s00249-002-0248-9. Epub 2002 Oct 2.
Ca(2+)-dependent adhesion molecules, cadherins, are critically involved in the barrier formation of epithelial layers. Adhesive strength depends on both the plasmalemmal concentration and adhesive affinity (affinity for trans interaction) of cadherins. In the present study we used recombinant vascular endothelial cadherin, VE-cadherin, as a reference to quantify the surface concentration of VE-cadherin in mouse microvascular endothelial cells by linear interpolation and regression analysis of immunosignals obtained with cell lysates dotted on nitrocellulose membranes. The affinity of trans interaction was determined by a novel mobility shift assay, in which soluble dimeric VE-cadherin ectodomains pass through a VE-cadherin affinity column. By these approaches we determined the trypsin-sensitive surface concentration of VE-cadherin to be 5 x 10(3) dimers/microm(2) cell surface and the dissociation constant K(D) to be about 0.8 x 10(-4) M. The low affinity of trans interaction in combination with high plasmalemmal concentration of VE-cadherins fulfils theoretical predictions for regulation of adhesion by a transmembrane cooperative linkage mechanism, in which the degree of lateral mobility (translational entropy) of cadherins in the plasma membrane determines the number of adhesive bonds and, hence, the strength of intercellular adhesion.
钙离子依赖的黏附分子,即钙黏蛋白,在形成上皮层屏障的过程中起着关键作用。黏附强度取决于钙黏蛋白的质膜浓度和黏附亲和力(对反式相互作用的亲和力)。在本研究中,我们使用重组血管内皮钙黏蛋白(VE-钙黏蛋白)作为参照,通过对点样于硝酸纤维素膜上的细胞裂解物所获得的免疫信号进行线性插值和回归分析,来定量小鼠微血管内皮细胞中VE-钙黏蛋白的表面浓度。反式相互作用的亲和力通过一种新型迁移率变动分析来测定,在该分析中,可溶性二聚体VE-钙黏蛋白胞外结构域通过一个VE-钙黏蛋白亲和柱。通过这些方法,我们确定VE-钙黏蛋白对胰蛋白酶敏感的表面浓度为5×10³二聚体/μm²细胞表面,解离常数K(D)约为0.8×10⁻⁴M。反式相互作用的低亲和力与VE-钙黏蛋白较高的质膜浓度相结合,符合通过跨膜协同连接机制调节黏附的理论预测,在该机制中,钙黏蛋白在质膜中的侧向迁移程度(平移熵)决定了黏附键的数量,进而决定了细胞间黏附的强度。