Fatty acid transport and transporters in muscle are critically regulated by Akt2

FEBS Lett. 2015 Sep 14;589(19 Pt B):2769-75. doi: 10.1016/j.febslet.2015.08.010. Epub 2015 Aug 18.

Abstract

Muscle contains various fatty acid transporters (CD36, FABPpm, FATP1, FATP4). Physiological stimuli (insulin, contraction) induce the translocation of all four transporters to the sarcolemma to enhance fatty acid uptake similarly to glucose uptake stimulation via glucose transporter-4 (GLUT4) translocation. Akt2 mediates insulin-induced, but not contraction-induced, GLUT4 translocation, but its role in muscle fatty acid transporter translocation is unknown. In muscle from Akt2-knockout mice, we observed that Akt2 is critically involved in both insulin-induced and contraction-induced fatty acid transport and translocation of fatty acid translocase/CD36 (CD36) and FATP1, but not of translocation of fatty acid-binding protein (FABPpm) and FATP4. Instead, Akt2 mediates intracellular retention of both latter transporters. Collectively, our observations reveal novel complexities in signaling mechanisms regulating the translocation of fatty acid transporters in muscle.

Keywords: Akt2; Contraction; Fatty acid translocase/CD36; Fatty acid transport; Glucose transporter-4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Fatty Acid Transport Proteins / metabolism*
  • Fatty Acid-Binding Proteins / metabolism*
  • Fatty Acids / metabolism*
  • Gene Expression Regulation, Enzymologic
  • Gene Knockout Techniques
  • Glucose / metabolism
  • Glucose Transporter Type 4 / metabolism
  • Insulin / metabolism
  • Mice
  • Muscles / cytology
  • Muscles / metabolism*
  • Phenotype
  • Phosphorylation
  • Protein Transport
  • Proto-Oncogene Proteins c-akt / deficiency
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Signal Transduction

Substances

  • Fatty Acid Transport Proteins
  • Fatty Acid-Binding Proteins
  • Fatty Acids
  • Glucose Transporter Type 4
  • Insulin
  • Akt2 protein, mouse
  • Proto-Oncogene Proteins c-akt
  • Glucose