González-Mariscal Lorenza, Raya-Sandino Arturo, González-González Laura, Hernández-Guzmán Christian
a Department of Physiology , Biophysics and Neuroscience, Center for Research and Advanced Studies (Cinvestav) , Mexico City , Mexico.
Tissue Barriers. 2018 Jan 2;6(1):e1414015. doi: 10.1080/21688370.2017.1414015. Epub 2018 Feb 8.
Tight junctions (TJs) are sites of cell-cell adhesion, constituted by a cytoplasmic plaque of molecules linked to integral proteins that form a network of strands around epithelial and endothelial cells at the uppermost portion of the lateral membrane. TJs maintain plasma membrane polarity and form channels and barriers that regulate the transit of ions and molecules through the paracellular pathway. This structure that regulates traffic between the external milieu and the organism is affected in numerous pathological conditions and constitutes an important target for therapeutic intervention. Here, we describe how a wide array of G protein-coupled receptors that are activated by diverse stimuli including light, ions, hormones, peptides, lipids, nucleotides and proteases, signal through heterotrimeric G proteins, arrestins and kinases to regulate TJs present in the blood-brain barrier, the blood-retinal barrier, renal tubular cells, keratinocytes, lung and colon, and the slit diaphragm of the glomerulus.
紧密连接(TJs)是细胞间黏附的位点,由与整合蛋白相连的分子组成的胞质斑块构成,这些整合蛋白在侧膜最上部围绕上皮细胞和内皮细胞形成一个链状网络。紧密连接维持质膜极性,并形成通道和屏障,调节离子和分子通过细胞旁途径的转运。这种调节外部环境与机体之间物质交换的结构在许多病理状态下会受到影响,并且是治疗干预的重要靶点。在此,我们描述了一系列由多种刺激激活的G蛋白偶联受体,这些刺激包括光、离子、激素、肽、脂质、核苷酸和蛋白酶,它们如何通过异源三聚体G蛋白、抑制蛋白和激酶进行信号传导,以调节血脑屏障、血视网膜屏障、肾小管细胞、角质形成细胞、肺和结肠以及肾小球裂孔隔膜中的紧密连接。