Visfatin, a novel adipokine, stimulates glucose uptake through the Ca2 +-dependent AMPK-p38 MAPK pathway in C2C12 skeletal muscle cells

J Mol Endocrinol. 2015 Jun;54(3):251-62. doi: 10.1530/JME-14-0274.

Abstract

Visfatin is a novel adipocytokine produced by visceral fat. In the present study, visfatin increased AMP-activated protein kinase (AMPK) phosphorylation in mouse C2C12 skeletal muscle cells. It also increased phosphorylation of the insulin receptor, whose knockdown blocked visfatin-induced AMPK phosphorylation and glucose uptake. Visfatin stimulated glucose uptake in differentiated skeletal muscle cells. However, inhibition of AMPKα2 with an inhibitor or with knockdown of AMPKα2 using siRNA blocked visfatin-induced glucose uptake, which indicates that visfatin stimulates glucose uptake through the AMPKα2 pathway. Visfatin increased the intracellular Ca(2) (+) concentration. STO-609, a calmodulin-dependent protein kinase kinase inhibitor, blocked visfatin-induced AMPK phosphorylation and glucose uptake. Visfatin-mediated activation of p38 MAPK was AMPKα2-dependent. Furthermore, both inhibition and knockdown of p38 MAPK blocked visfatin-induced glucose uptake. Visfatin increased glucose transporter type 4 (GLUT4) mRNA and protein levels. In addition, visfatin stimulated the translocation of GLUT4 to the plasma membrane, and this effect was suppressed by AMPKα2 inhibition. The present results indicate that visfatin plays an important role in glucose metabolism via the Ca(2) (+)-mediated AMPK-p38 MAPK pathway.

Keywords: AMPK; adipokine; calcium; diabetes; glucose transport.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism*
  • Acetyl-CoA Carboxylase / metabolism
  • Animals
  • Biological Transport
  • Calcium Signaling
  • Cell Line
  • Cytokines / physiology*
  • Enzyme Activation
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism
  • MAP Kinase Signaling System
  • Mice
  • Myoblasts, Skeletal / metabolism*
  • Nicotinamide Phosphoribosyltransferase / physiology*
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Protein Transport
  • Rats
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Cytokines
  • Glucose Transporter Type 4
  • Slc2a4 protein, mouse
  • Nicotinamide Phosphoribosyltransferase
  • nicotinamide phosphoribosyltransferase, mouse
  • Prkaa2 protein, mouse
  • p38 Mitogen-Activated Protein Kinases
  • AMP-Activated Protein Kinases
  • Acetyl-CoA Carboxylase
  • Glucose