4.7 Review

Tight Junctions as Targets and Effectors of Mucosal Immune Homeostasis

出版社

ELSEVIER INC
DOI: 10.1016/j.jcmgh.2020.04.001

关键词

Intestinal Permeability; Barrier; Myosin Light Chain Kinase; Enteric Infection; Inflammatory Bowel Disease; Graft-Versus-Host Disease; Pore Pathway; Leak Pathway; Claudin

资金

  1. NIH [R01DK61931, R01DK68271, R24DK099803]
  2. Harvard Digestive Disease Center [P30DK034854]
  3. Department of Defense [CDMRP PR181271]
  4. National Natural Science Foundation of China [81800464]

向作者/读者索取更多资源

Defective epithelial barrier function is present in maladies including epidermal burn injury, environmental lung damage, renal tubular disease, and a range of immune-mediated and infectious intestinal disorders. When the epithelial surface is intact, the paracellular pathway be-tween cells is sealed by the tight junction. However, permeability of tight junctions varies widely across tissues and can be markedly impacted by disease. For example, tight junctions within the skin and urinary bladder are largely impermeant and their permeability is not regulated. In contrast, tight junctions of the proximal renal tubule and intestine are selectively permeable to water and solutes on the basis of their biophysical characteristics and, in the gut, can be regulated by the immune system with remarkable specificity. Conversely, modulation of tight junction barrier conductance, especially within the gastrointestinal tract, can impact immune homeostasis and diverse pathologies. Thus, tight junctions are both effectors and targets of immune regulation. Using the gastrointestinal tract as an example, this review explores current understanding of this complex interplay between tight junctions and immunity.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据