González-Mariscal Lorenza, Tapia Rocio, Chamorro David
Center for Research and Advanced Studies (Cinvestav), Department of Physiology, Biophysics and Neuroscience, Ave. Instituto Politécnico Nacional 2508, México D. F. 07360, México.
Biochim Biophys Acta. 2008 Mar;1778(3):729-56. doi: 10.1016/j.bbamem.2007.08.018. Epub 2007 Sep 4.
Tight junctions (TJs) regulate the passage of ions and molecules through the paracellular pathway in epithelial and endothelial cells. TJs are highly dynamic structures whose degree of sealing varies according to external stimuli, physiological and pathological conditions. In this review we analyze how the crosstalk of protein kinase C, protein kinase A, myosin light chain kinase, mitogen-activated protein kinases, phosphoinositide 3-kinase and Rho signaling pathways is involved in TJ regulation triggered by diverse stimuli. We also report how the phosphorylation of the main TJ components, claudins, occludin and ZO proteins, impacts epithelial and endothelial cell function.
紧密连接(TJs)调节离子和分子通过上皮细胞和内皮细胞的细胞旁途径的运输。紧密连接是高度动态的结构,其密封程度根据外部刺激、生理和病理状况而变化。在本综述中,我们分析了蛋白激酶C、蛋白激酶A、肌球蛋白轻链激酶、丝裂原活化蛋白激酶、磷酸肌醇3激酶和Rho信号通路的相互作用如何参与由多种刺激引发的紧密连接调节。我们还报告了紧密连接主要成分(闭合蛋白、封闭蛋白和ZO蛋白)的磷酸化如何影响上皮细胞和内皮细胞的功能。