Division of Cell Biology, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Japan.
Ann N Y Acad Sci. 2012 Jun;1257:54-8. doi: 10.1111/j.1749-6632.2012.06486.x.
Tricellular tight junctions (tTJs) are specialized structural variants of tight junctions that restrict the free diffusion of solutes at the extracellular space of tricellular contacts. Their presence at cell corners, situated in the angles between three adjacent epithelial cells, was identified early by electron microscopy, but despite their potential importance, tTJs have been generally ignored in epithelial cell biology. Tricellulin was the first molecular component of tTJs shown to be involved in their formation and in epithelial barrier function. However, the precise molecular organization and function of tTJs are still largely unknown. Recently, we identified the lipolysis-stimulated lipoprotein receptor (LSR) as a tTJ-associated membrane protein. LSR recruits tricellulin to tTJs, suggesting that the LSR-tricellulin system plays a key role in tTJ formation. In this paper, we summarize the identification and characterization of LSR as a molecular component of tTJs.
三细胞紧密连接(tTJs)是紧密连接的特化结构变体,限制了细胞外空间中溶质的自由扩散。它们位于三个相邻上皮细胞的角部,即细胞连接处,这一位置早在电子显微镜下就被识别出来,但尽管它们具有潜在的重要性,tTJs 在上皮细胞生物学中通常被忽视。桥粒芯糖蛋白被认为是第一个参与 tTJs 形成和上皮屏障功能的 tTJs 分子组成部分。然而,tTJs 的精确分子组成和功能仍在很大程度上未知。最近,我们鉴定出脂肪酶刺激的脂蛋白受体(LSR)是一种与 tTJ 相关的膜蛋白。LSR 将桥粒芯糖蛋白募集到 tTJs 上,这表明 LSR-桥粒芯糖蛋白系统在 tTJ 形成中发挥关键作用。在本文中,我们总结了 LSR 作为 tTJs 分子组成部分的鉴定和特征。