Over-expression of AQP7 contributes to improve insulin resistance in adipocytes

Exp Cell Res. 2012 Nov 1;318(18):2377-84. doi: 10.1016/j.yexcr.2012.07.016. Epub 2012 Aug 2.

Abstract

Objective: Aquaglyceroporin 7 (AQP7) is required for efflux of glycerol from adipocytes. In this study, we aimed to analyze expression profiles of AQP7 in the different differentiation phases of adipocytes and to investigate the role of AQP7 in the insulin resistance of adipocytes.

Methods: 3T3-L1 pre-adipocyte cells were induced to be fully differentiated adipocytes and then insulin resistance was induced by Dexamethasone (DXM) or TNF-α. Adenovirus vector with over-expression AQP7 (Ad-AQP7) was constructed and transfected into adipocytes. The expression level of AQP7 and phosphorylated PKB (p-PKB) were measured. The glycerol released from adipocytes and glucose consuming rate were tested too.

Results: AQP7 expression was gradually up-regulated along with the differentiation processing of 3T3-L1 preadipocytes, which was consistent with the expression level of p-PKB. Dexamethasone down-regulated the expression of AQP7, p-PKB and the glycerol content in adipocytes. Over-expression of AQP7 by transfecting Ad-AQP7 to insulin resistant adipocytes restored the phosphorylation of PKB and attenuated the glycerol secretion and glucose consuming rate of adipocytes.

Conclusions: AQP7 is down-regulated in adipocytes with insulin resistance. The over-expression of AQP7 contributes to improve insulin resistance in adipocytes, which is potentially correlated with the increased phosphorylation of PKB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Phosphoinositide-Dependent Protein Kinases
  • 3T3-L1 Cells
  • Adipocytes / cytology*
  • Adipocytes / metabolism
  • Animals
  • Aquaporins / genetics*
  • Aquaporins / metabolism
  • Cell Differentiation
  • Dexamethasone / pharmacology
  • Down-Regulation
  • Insulin Resistance / genetics*
  • Mice
  • Phosphorylation
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • RNA, Messenger / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Aqp7 protein, mouse
  • Aquaporins
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Dexamethasone
  • 3-Phosphoinositide-Dependent Protein Kinases
  • Protein Serine-Threonine Kinases