Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, 48109, United States.
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, 48109, United States
J Cell Sci. 2019 Nov 21;132(22):jcs229286. doi: 10.1242/jcs.229286.
Epithelial cells form tissues that generate biological barriers in the body. Tight junctions (TJs) are responsible for maintaining a selectively permeable seal between epithelial cells, but little is known about how TJs dynamically remodel in response to physiological forces that challenge epithelial barrier function, such as cell shape changes (e.g. during cell division) or tissue stretching (e.g. during developmental morphogenesis). In this Review, we first introduce a framework to think about TJ remodeling across multiple scales: from molecular dynamics, to strand dynamics, to cell- and tissue-scale dynamics. We then relate knowledge gained from global perturbations of TJs to emerging information about local TJ remodeling events, where transient localized Rho activation and actomyosin-mediated contraction promote TJ remodeling to repair local leaks in barrier function. We conclude by identifying emerging areas in the field and propose ideas for future studies that address unanswered questions about the mechanisms that drive TJ remodeling.
上皮细胞形成组织,在体内产生生物屏障。紧密连接(TJ)负责维持上皮细胞之间具有选择性渗透性的密封,但对于 TJ 如何动态重塑以响应挑战上皮屏障功能的生理力知之甚少,例如细胞形状变化(例如在细胞分裂期间)或组织拉伸(例如在发育形态发生期间)。在这篇综述中,我们首先介绍了一个跨多个尺度思考 TJ 重塑的框架:从分子动力学到链动力学,再到细胞和组织尺度动力学。然后,我们将从全局扰动 TJ 中获得的知识与关于局部 TJ 重塑事件的新兴信息联系起来,其中瞬时局部 Rho 激活和肌动球蛋白介导的收缩促进 TJ 重塑,以修复屏障功能局部泄漏。最后,我们确定了该领域的新兴领域,并提出了未来研究的想法,以解决关于驱动 TJ 重塑的机制的未解答问题。