基因敲除
肾
体内
纤维化
细胞生长
肾脏发育
内分泌学
内科学
急性肾损伤
生物
医学
病理
癌症研究
细胞培养
基因
生物技术
胚胎干细胞
遗传学
生物化学
作者
Roland Schmitt,Arnaud Marlier,Lloyd G. Cantley
出处
期刊:Journal of The American Society of Nephrology
日期:2008-12-01
卷期号:19 (12): 2375-2383
被引量:86
标识
DOI:10.1681/asn.2008010035
摘要
Recovery after acute kidney injury is impaired in the elderly, but mechanistic information regarding why this occurs is limited. In this study, aged mouse kidneys displayed a reduced epithelial proliferative reserve in vivo and in vitro. Microarray analysis identified increased expression of zinc-alpha (2)-glycoprotein (Zag) in aged proximal tubular cells. The addition of recombinant Zag to primary renal epithelial cell cultures decreased proliferation, whereas knockdown of Zag increased proliferation. In vivo, systemic small interference RNA suppressed expression of Zag in the mouse proximal tubule; this increased the rate of epithelial cell proliferation after renal ischemia/reperfusion in aged mice but also increased parenchymal fibrosis. These results demonstrate that increased Zag expression in the aged kidney acts to suppress the proliferative response to injury and introduce Zag as a modifier of the aging phenotype.
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