4.5 Article

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

Journal

EXPERIMENTAL GERONTOLOGY
Volume 51, Issue -, Pages 71-81

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exger.2013.12.016

Keywords

Connexin43; AMPK; mTOR; Mesangial cell senescence; Diabetic nephropathy

Funding

  1. National Basic Research Program of China (973 Program) [2013CB530800]
  2. National Natural Science Foundation of China [81070267, 81171645]
  3. 863 program [2012AA02A512]

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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.

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