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α(E)-连环蛋白调节肾上皮细胞中骨形态发生蛋白-7的表达和迁移。

α(E)-catenin regulates BMP-7 expression and migration in renal epithelial cells.

作者信息

Nichols LaNita A, Slusarz Anna, Grunz-Borgmann Elizabeth A, Parrish Alan R

机构信息

Medical Pharmacology and Physiology, School of Medicine, University of Missouri, Columbia, Mo., USA.

出版信息

Am J Nephrol. 2014;39(5):409-17. doi: 10.1159/000362250. Epub 2014 May 6.

Abstract

BACKGROUND

The aging kidney has a decreased ability to repair following injury. We have shown a loss in expression of α-catenin in the aging rat kidney and hypothesize that decreased α-catenin expression in tubular epithelial cells results in diminished repair capacity.

METHODS

In an effort to elucidate alterations due to the loss of α-catenin, we generated NRK-52E cell lines with stable knockdown of α(E)-catenin.

RESULTS

α(E)-catenin knockdown resulted in decreased wound repair due to alterations in cell migration. Analysis of gene expression in the α(E)-catenin knockdown cells demonstrated almost a complete loss of bone morphogenetic protein-7 (BMP-7) expression that was associated with decreased phospho-Smad1/5/8 staining. However, addition of exogenous BMP-7 increased phospho-Smad1/5/8, suggesting that the BMP-7 pathway remained intact in C2 cells. Given the potential role of BMP-7 in repair, we investigated its role in wound repair. Inhibition of BMP-7 decreased repair in non-targeted control cells; conversely, exogenous BMP-7 restored repair in α(E)-catenin knockdown cells to control levels.

CONCLUSIONS

Taken together, the data suggests that the loss of α(E)-catenin expression and subsequent downregulation of BMP-7 is a mechanism underlying the altered migration of tubular epithelial cells that contributes to the inability of the aging kidney to repair following injury.

摘要

背景

衰老的肾脏在损伤后修复能力下降。我们已证实在衰老大鼠肾脏中α-连环蛋白的表达缺失,并推测肾小管上皮细胞中α-连环蛋白表达的降低导致修复能力减弱。

方法

为了阐明由于α-连环蛋白缺失引起的变化,我们构建了稳定敲低α(E)-连环蛋白的NRK-52E细胞系。

结果

α(E)-连环蛋白敲低导致伤口修复能力下降,这是由于细胞迁移的改变所致。对α(E)-连环蛋白敲低细胞中的基因表达分析表明,骨形态发生蛋白-7(BMP-7)的表达几乎完全丧失,这与磷酸化Smad1/5/8染色减少相关。然而,添加外源性BMP-7可增加磷酸化Smad1/5/8,这表明BMP-7信号通路在C2细胞中保持完整。鉴于BMP-7在修复中的潜在作用,我们研究了其在伤口修复中的作用。抑制BMP-7会降低非靶向对照细胞的修复能力;相反,外源性BMP-7可将α(E)-连环蛋白敲低细胞中的修复能力恢复到对照水平。

结论

综上所述,数据表明α(E)-连环蛋白表达的缺失以及随后BMP-7的下调是肾小管上皮细胞迁移改变的一种机制,这导致衰老的肾脏在损伤后无法修复。

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