Institute of Veterinary Physiology, Freie Universität Berlin, Berlin, Germany; and.
Institute of Pathology and Neuropathology, University of Tuebingen, Tuebingen, Germany.
FASEB J. 2019 Apr;33(4):5312-5319. doi: 10.1096/fj.201801451RR. Epub 2019 Jan 15.
Claudins (cldns) represent the largest family of transmembrane tight junction (TJ) proteins, determining organ-specific epithelial barrier properties. Because methods for the analysis of multiple cldn interaction are limited, we have established the heterologous Xenopus laevis oocyte expression system for TJ protein assembly and interaction analysis. Oocytes were injected with cRNA encoding human cldn-1, -2, or -3 or with a combination of these and were incubated in pairs for interaction analysis. Immunoblotting and immunohistochemistry were performed, and membrane contact areas were analyzed morphometrically and by freeze fracture electron microscopy. Cldns were specifically detected in membranes of expressing oocytes, and coincubation of oocytes resulted in adhesive contact areas that increased with incubation time. Adjacent membrane areas revealed specific cldn signals, including "kissing-point"-like structures representing homophilic trans-interactions of cldns. Contact areas of oocytes expressing a combination markedly exceeded those expressing single cldns, indicating effects on adhesion. Ultrastructural analysis revealed a self-assembly of TJ strands and a cldn-specific strand morphology.-Vitzthum, C., Stein, L., Brunner, N., Knittel, R., Fallier-Becker, P., Amasheh, S. Xenopus oocytes as a heterologous expression system for analysis of tight junction proteins.
紧密连接蛋白(Claudins,cldns)是跨膜紧密连接(Tight Junction,TJ)蛋白家族中最大的成员,决定了器官特异性上皮屏障的特性。由于分析多个 cldn 相互作用的方法有限,我们建立了异源非洲爪蟾卵母细胞表达系统,用于 TJ 蛋白组装和相互作用分析。卵母细胞被注射编码人 cldn-1、-2 或 -3 的 cRNA 或这些蛋白的组合,并进行共孵育以进行相互作用分析。进行免疫印迹和免疫组织化学分析,并通过形态计量学和冷冻断裂电子显微镜分析膜接触区。cldn 特异性地在表达卵母细胞的膜中被检测到,并且共孵育导致接触面积随着孵育时间的增加而增加。相邻的膜区域显示出特定的 cldn 信号,包括代表 cldn 同源相互作用的“亲吻点”样结构。表达组合的 cldn 的卵母细胞的接触区明显超过表达单个 cldn 的卵母细胞的接触区,表明对粘附有影响。超微结构分析显示 TJ 链的自组装和 cldn 特异性链形态。-Vitzthum, C., Stein, L., Brunner, N., Knittel, R., Fallier-Becker, P., Amasheh, S. 非洲爪蟾卵母细胞作为分析紧密连接蛋白的异源表达系统。