Tight junction biology and kidney dysfunction

被引:141
作者
Lee, DBN
Huang, E
Ward, HJ
机构
[1] VA Med Ctr, Dept Med 111, Sepulveda, CA 91343 USA
[2] Univ Calif Los Angeles, Ctr Med, Div Nephrol, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Ctr Med, Vet Affairs Greater Los Angeles Healthcare Syst, VISN 22, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, King Drew Med Ctr, Los Angeles, CA 90059 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90059 USA
关键词
kidney disease; zonula occludens;
D O I
10.1152/ajprenal.00052.2005
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Tight junction biology and kidney dysfunction. Am J Physiol Renal Physiol 290: F20-F34, 2006; doi:10.1152/ajprenal.00052.2005.- The epithelial tight junction (TJ) has three major functions. As a "gate," it serves as a regulatory barrier separating and maintaining biological fluid compartments of different composition. As a " fence," it generates and maintains the apicobasal polarity of cells that form the confluent epithelium. Finally, the TJ proteins form a trafficking and signaling platform that regulates cell growth, proliferation, differentiation, and dedifferentiation. Six examples are selected that illustrate the emerging link between TJ dysfunction and kidney disease. First, the glomerular slit diaphragm (GSD) is evolved, in part, from the TJ and, on maturation, exhibits all three functions of the TJ. GSD dysfunction leads to proteinuria and, in some instances, podocyte dedifferentiation and proliferation. Second, accumulating evidence supports epithelial-mesenchymal transformation (EMT) as a major player in renal fibrosis, the final common pathway that leads to end-stage renal failure. EMT is characterized by a loss of cell-cell contact and apicobasal polarity, which are hallmarks of TJ dysfunction. Third, in autosomal dominant polycystic kidney disease, mutations of the polycystins may disrupt their known interactions with the apical junction complex, of which the TJ is a major component. This can lead to disturbances in epithelial polarity regulation with consequent abnormal tubulogenesis and cyst formation. Fourth, evidence for epithelial barrier and polarity dysregulation in the pathogenesis of ischemic acute renal failure will be summarized. Fifth, the association between mutations of paracellin-1, the first TJ channel identified, and clinical disorders of magnesium and calcium wasting and bovine renal fibrosis will be used to highlight an integral TJ protein that can serve multiple TJ functions. Finally, the role of WNK4 protein kinase in shunting chloride across the TJ of the distal nephron will be addressed.
引用
收藏
页码:F20 / F34
页数:15
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