c-Cbl-deficient mice have reduced adiposity, higher energy expenditure, and improved peripheral insulin action

J Clin Invest. 2004 Nov;114(9):1326-33. doi: 10.1172/JCI21480.

Abstract

Casitas b-lineage lymphoma (c-Cbl) is an E3 ubiquitin ligase that has an important role in regulating the degradation of cell surface receptors. In the present study we have examined the role of c-Cbl in whole-body energy homeostasis. c-Cbl-/- mice exhibited a profound increase in whole-body energy expenditure as determined by increased core temperature and whole-body oxygen consumption. As a consequence, these mice displayed a decrease in adiposity, primarily due to a reduction in cell size despite an increase in food intake. These changes were accompanied by a significant increase in activity (2- to 3-fold). In addition, c-Cbl-/- mice displayed a marked improvement in whole-body insulin action, primarily due to changes in muscle metabolism. We observed increased protein levels of the insulin receptor (4-fold) and uncoupling protein-3 (2-fold) in skeletal muscle and a significant increase in the phosphorylation of AMP-activated protein kinase and acetyl-CoA carboxylase. These findings suggest that c-Cbl plays an integral role in whole-body fuel homeostasis by regulating whole-body energy expenditure and insulin action.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases
  • Acetyl-CoA Carboxylase / metabolism
  • Adipocytes / metabolism
  • Adipose Tissue / metabolism*
  • Animals
  • Body Composition
  • Body Temperature
  • Body Weight
  • Carrier Proteins / metabolism
  • Cell Membrane / metabolism
  • Energy Metabolism*
  • Female
  • Glucose / metabolism
  • In Situ Hybridization
  • Insulin / metabolism*
  • Ion Channels
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Electron
  • Mitochondria / metabolism
  • Mitochondrial Proteins
  • Multienzyme Complexes / metabolism
  • Muscle, Skeletal / metabolism
  • Muscles / metabolism
  • Oxygen Consumption
  • Phosphorylation
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-cbl
  • Receptor, Insulin / metabolism
  • Time Factors
  • Ubiquitin-Protein Ligases / genetics*
  • Ubiquitin-Protein Ligases / physiology*
  • Uncoupling Protein 3

Substances

  • Carrier Proteins
  • Insulin
  • Ion Channels
  • Mitochondrial Proteins
  • Multienzyme Complexes
  • Proto-Oncogene Proteins
  • Ucp3 protein, mouse
  • Uncoupling Protein 3
  • Proto-Oncogene Proteins c-cbl
  • Ubiquitin-Protein Ligases
  • Receptor, Insulin
  • Protein Serine-Threonine Kinases
  • AMP-Activated Protein Kinases
  • Cbl protein, mouse
  • Acetyl-CoA Carboxylase
  • Glucose