Systems-level analysis of insulin action in mouse strains provides insight into tissue- and pathway-specific interactions that drive insulin resistance

Research output: Contribution to journalJournal articleResearchpeer-review

  • Marin E Nelson
  • Søren Madsen
  • Kristen C Cooke
  • Fritzen, Andreas Mæchel
  • Ida H Thorius
  • Stewart W C Masson
  • Luke Carroll
  • Fiona C Weiss
  • Marcus M Seldin
  • Meg Potter
  • Samantha L Hocking
  • Daniel J Fazakerley
  • Amanda E Brandon
  • Senthil Thillainadesan
  • Alistair M Senior
  • Gregory J Cooney
  • Jacqueline Stöckli
  • David E James

Skeletal muscle and adipose tissue insulin resistance are major drivers of metabolic disease. To uncover pathways involved in insulin resistance, specifically in these tissues, we leveraged the metabolic diversity of different dietary exposures and discrete inbred mouse strains. This revealed that muscle insulin resistance was driven by gene-by-environment interactions and was strongly correlated with hyperinsulinemia and decreased levels of ten key glycolytic enzymes. Remarkably, there was no relationship between muscle and adipose tissue insulin action. Adipocyte size profoundly varied across strains and diets, and this was strongly correlated with adipose tissue insulin resistance. The A/J strain, in particular, exhibited marked adipocyte insulin resistance and hypertrophy despite robust muscle insulin responsiveness, challenging the role of adipocyte hypertrophy per se in systemic insulin resistance. These data demonstrate that muscle and adipose tissue insulin resistance can occur independently and underscore the need for tissue-specific interrogation to understand metabolic disease.

Original languageEnglish
JournalCell Metabolism
Volume34
Issue number2
Pages (from-to)227-239.e6
Number of pages20
ISSN1550-4131
DOIs
Publication statusPublished - 2022
Externally publishedYes

Bibliographical note

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