Renal Tubule Repair: Is Wnt/-Catenin a Friend or Foe?

被引:27
|
作者
Gewin, Leslie S. [1 ,2 ]
机构
[1] Vanderbilt Univ, Div Nephrol, Dept Med, Med Ctr, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Cell & Dev Biol, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
kidney injury; renal fibrosis; epithelial injury; TO-MESENCHYMAL TRANSITION; EPITHELIAL-CELLS REPAIR; BETA-CATENIN; METANEPHRIC MESENCHYME; NEPHRON PROGENITORS; SIGNALING PATHWAY; OXIDATIVE STRESS; MAMMALIAN KIDNEY; STEM-CELLS; INJURY;
D O I
10.3390/genes9020058
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Wnt/beta-catenin signaling is extremely important for proper kidney development. This pathway is also upregulated in injured renal tubular epithelia, both in acute kidney injury and chronic kidney disease. The renal tubular epithelium is an important target of kidney injury, and its response (repair versus persistent injury) is critical for determining whether tubulointerstitial fibrosis, the hallmark of chronic kidney disease, develops. This review discusses how Wnt/-catenin signaling in the injured tubular epithelia promotes either repair or fibrosis after kidney injury. There is data suggesting that epithelial Wnt/-catenin signaling is beneficial in acute kidney injury and important in tubular progenitors responsible for epithelial repair. The role of Wnt/-catenin signaling in chronically injured epithelia is less clear. There is convincing data that Wnt/-catenin signaling in interstitial fibroblasts and pericytes contributes to the extracellular matrix accumulation that defines fibrosis. However, some recent studies question whether Wnt/-catenin signaling in chronically injured epithelia actually promotes fibrosis or repair.
引用
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页数:12
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