Hepatic protein tyrosine phosphatase receptor gamma links obesity-induced inflammation to insulin resistance

Nat Commun. 2017 Nov 28;8(1):1820. doi: 10.1038/s41467-017-02074-2.

Abstract

Obesity-induced inflammation engenders insulin resistance and type 2 diabetes mellitus (T2DM) but the inflammatory effectors linking obesity to insulin resistance are incompletely understood. Here, we show that hepatic expression of Protein Tyrosine Phosphatase Receptor Gamma (PTPR-γ) is stimulated by inflammation in obese/T2DM mice and positively correlates with indices of inflammation and insulin resistance in humans. NF-κB binds to the promoter of Ptprg and is required for inflammation-induced PTPR-γ expression. PTPR-γ loss-of-function lowers glycemia and insulinemia by enhancing insulin-stimulated suppression of endogenous glucose production. These phenotypes are rescued by re-expression of Ptprg only in liver of mice lacking Ptprg globally. Hepatic PTPR-γ overexpression that mimics levels found in obesity is sufficient to cause severe hepatic and systemic insulin resistance. We propose hepatic PTPR-γ as a link between obesity-induced inflammation and insulin resistance and as potential target for treatment of T2DM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Blood Glucose
  • Cell Line
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / metabolism*
  • Female
  • Gene Expression
  • Gene Expression Profiling
  • Hep G2 Cells
  • Humans
  • Inflammation / metabolism
  • Insulin / blood
  • Insulin Resistance / physiology*
  • Interleukin-6 / metabolism
  • Lipid Metabolism
  • Lipopolysaccharides / adverse effects
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • Middle Aged
  • Models, Animal
  • NF-kappa B / metabolism
  • Obesity / blood
  • Obesity / complications
  • Obesity / metabolism*
  • Protein Tyrosine Phosphatases / metabolism
  • RNA, Messenger / biosynthesis
  • Receptor-Like Protein Tyrosine Phosphatases / genetics
  • Receptor-Like Protein Tyrosine Phosphatases / metabolism*
  • Sirtuin 1 / metabolism

Substances

  • Blood Glucose
  • Insulin
  • Interleukin-6
  • Lipopolysaccharides
  • NF-kappa B
  • RNA, Messenger
  • Protein Tyrosine Phosphatases
  • Receptor-Like Protein Tyrosine Phosphatases
  • Sirt1 protein, mouse
  • Sirtuin 1