Revisiting the roles of glucose transporters in skeletal muscle physiology: is GLUT10 a novel player?

Biochem Biophys Res Commun. 2024 Feb 12:696:149494. doi: 10.1016/j.bbrc.2024.149494. Epub 2024 Jan 8.

Abstract

Skeletal muscle is the largest metabolic tissue responsible for systemic glucose handling. Glucose uptake into skeletal tissue is highly dynamic and delicately regulated, in part through the controlled expression and subcellular trafficking of multiple types of glucose transporters. Although the roles of GLUT4 in skeletal muscle metabolism are well established, the physiological significance of other, seemingly redundant, glucose transporters remain incompletely understood. Nonetheless, recent studies have shed light on the roles of several glucose transporters, such as GLUT1 and GLUT10, in skeletal muscle. Mice experiments suggest that GLUT10 could be a novel player in skeletal muscle metabolism in the context of mechanical overload, which is in line with the meta-analytical results of gene expression changes after resistance exercise in humans. Herein we discuss the knowns, unknowns, and implications of these recent findings.

Keywords: GLUT10; Glucose transporter; Glucose uptake; Resistance exercise; Skeletal muscle.

Publication types

  • Review

MeSH terms

  • Animals
  • Biological Transport
  • Glucose / metabolism
  • Glucose Transport Proteins, Facilitative* / genetics
  • Glucose Transport Proteins, Facilitative* / metabolism
  • Glucose Transporter Type 1 / genetics
  • Glucose Transporter Type 1 / metabolism
  • Glucose Transporter Type 4 / genetics
  • Glucose Transporter Type 4 / metabolism
  • Humans
  • Insulin / metabolism
  • Mice
  • Monosaccharide Transport Proteins* / genetics
  • Muscle, Skeletal / metabolism

Substances

  • Glucose Transport Proteins, Facilitative
  • Monosaccharide Transport Proteins
  • Glucose
  • Glucose Transporter Type 4
  • Insulin
  • Glucose Transporter Type 1