AMPK-mediated downregulation of connexin43 and premature senescence of mesangial cells under high-glucose conditions

被引:36
作者
Guo, Ya-Nan [1 ]
Wang, Jing-Chao [1 ,2 ]
Cai, Guang-Yan [1 ]
Hu, Xiao [1 ]
Cui, Shao-Yuan [1 ]
Lv, Yang [1 ]
Yin, Zhong [1 ]
Fu, Bo [1 ]
Hong, Quan [1 ]
Chen, Xiang-Mei [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, State Key Lab Kidney Dis, Dept Nephrol, Beijing 100853, Peoples R China
[2] Hebei Med Univ, Hosp 3, Shijiazhuang, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Connexin43; AMPK; mTOR; Mesangial cell senescence; Diabetic nephropathy; ENDOTHELIAL-CELLS; DIABETIC-NEPHROPATHY; RENAL HYPERTROPHY; GAP-JUNCTIONS; RAPAMYCIN; KINASE; COMMUNICATION; EXPRESSION; METFORMIN; ADHESION;
D O I
10.1016/j.exger.2013.12.016
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Diabetic nephropathy is associated with premature senescence. Our previous study showed that glomerular mesangial cells (GMCs) appeared to take on senescent phenotypes under high-glucose conditions in conjunction with the downregulation of connexin43 (Cx43). In this study, we investigated whether AMPK-mediated Cx43 expression and premature senescence in diabetic nephropathy are associated with mTOR activation. From in vivo and in vitro studies, we found decreased expression of Cx43 and p-AMPK but increased expression of p21 both in the glomeruli of diabetic nephropathy and in primary GMCs cultured in high glucose. Activating AMPK or inhibiting mTOR prevented the downregulation of Cx43 and reversed GMC senescence. Dominant-negative AMPK expression both reduced Cx43 expression and induced GMC senescence. Furthermore, AMPK regulated Cx43 expression and GMC senescence mainly through the inhibition of mTOR, although other pathways cannot be ruled out. This study demonstrated that AMPK signaling pathways play an important role in the regulation of the Cx43 expression that accompanies GMC senescence under high-glucose conditions. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:71 / 81
页数:11
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