肌球蛋白轻链激酶/ Rho 激酶对肠道黏膜屏障的调节。
The Regulation of Intestinal Mucosal Barrier by Myosin Light Chain Kinase/Rho Kinases.
机构信息
Department of Animal and Avian Sciences, College of Agriculture and Natural Resources, University of Maryland, College Park, MD 20742, USA.
Department of Clinical Sciences, Comparative Medicine Institute, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607, USA.
出版信息
Int J Mol Sci. 2020 May 18;21(10):3550. doi: 10.3390/ijms21103550.
The intestinal epithelial apical junctional complex, which includes tight and adherens junctions, contributes to the intestinal barrier function via their role in regulating paracellular permeability. Myosin light chain II (MLC-2), has been shown to be a critical regulatory protein in altering paracellular permeability during gastrointestinal disorders. Previous studies have demonstrated that phosphorylation of MLC-2 is a biochemical marker for perijunctional actomyosin ring contraction, which increases paracellular permeability by regulating the apical junctional complex. The phosphorylation of MLC-2 is dominantly regulated by myosin light chain kinase- (MLCK-) and Rho-associated coiled-coil containing protein kinase- (ROCK-) mediated pathways. In this review, we aim to summarize the current state of knowledge regarding the role of MLCK- and ROCK-mediated pathways in the regulation of the intestinal barrier during normal homeostasis and digestive diseases. Additionally, we will also suggest potential therapeutic targeting of MLCK- and ROCK-associated pathways in gastrointestinal disorders that compromise the intestinal barrier.
肠上皮顶端连接复合体,包括紧密连接和黏附连接,通过调节细胞旁通透性在肠道屏障功能中发挥作用。肌球蛋白轻链 II(MLC-2)已被证明是在胃肠道疾病期间改变细胞旁通透性的关键调节蛋白。先前的研究表明,MLC-2 的磷酸化是近连接肌动球蛋白环收缩的生化标志物,通过调节顶端连接复合体增加细胞旁通透性。MLC-2 的磷酸化主要受肌球蛋白轻链激酶-(MLCK-)和 Rho 相关卷曲螺旋蛋白激酶-(ROCK-)介导的途径调节。在这篇综述中,我们旨在总结目前关于 MLCK-和 ROCK 介导的途径在正常稳态和消化性疾病期间调节肠道屏障的作用的知识状态。此外,我们还将提出针对胃肠道疾病中破坏肠道屏障的 MLCK-和 ROCK 相关途径的潜在治疗靶向。