SDF-1 Is an Autocrine Insulin-Desensitizing Factor in Adipocytes

Diabetes. 2018 Jun;67(6):1068-1078. doi: 10.2337/db17-0706. Epub 2018 Mar 26.

Abstract

Insulin desensitization occurs not only under the obese diabetic condition but also in the fasting state. However, little is known about the common secretory factor(s) that are regulated under these two insulin-desensitized conditions. Here, using database analysis and in vitro and in vivo experiments, we identified stromal derived factor-1 (SDF-1) as an insulin-desensitizing factor in adipocytes, overexpressed in both fasting and obese adipose tissues. Exogenously added SDF-1 induced extracellular signal-regulated kinase signal, which phosphorylated and degraded IRS-1 protein in adipocytes, decreasing insulin-mediated signaling and glucose uptake. In contrast, knockdown of endogenous SDF-1 or inhibition of its receptor in adipocytes markedly increased IRS-1 protein levels and enhanced insulin sensitivity, indicating the autocrine action of SDF-1. In agreement with these findings, adipocyte-specific ablation of SDF-1 enhanced insulin sensitivity in adipose tissues and in the whole body. These results point to a novel regulatory mechanism of insulin sensitivity mediated by adipose autocrine SDF-1 action and provide a new insight into the process of insulin desensitization in adipocytes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes, Brown / metabolism
  • Adipocytes, Brown / pathology
  • Adipocytes, White / metabolism*
  • Adipocytes, White / pathology
  • Animals
  • Cells, Cultured
  • Chemokine CXCL12 / antagonists & inhibitors
  • Chemokine CXCL12 / genetics
  • Chemokine CXCL12 / metabolism*
  • Diet, High-Fat / adverse effects
  • Female
  • Gene Expression Regulation*
  • Humans
  • Insulin Receptor Substrate Proteins / genetics
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance*
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Mice
  • Mice, Knockout
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Obesity / etiology
  • Obesity / metabolism*
  • Obesity / pathology
  • Organ Specificity
  • RNA Interference

Substances

  • CXCL12 protein, human
  • Chemokine CXCL12
  • Cxcl12 protein, mouse
  • IRS1 protein, human
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse