Activation of AMP-activated protein kinase rapidly suppresses multiple pro-inflammatory pathways in adipocytes including IL-1 receptor-associated kinase-4 phosphorylation

Mol Cell Endocrinol. 2017 Jan 15:440:44-56. doi: 10.1016/j.mce.2016.11.010. Epub 2016 Nov 11.

Abstract

Inflammation of adipose tissue in obesity is associated with increased IL-1β, IL-6 and TNF-α secretion and proposed to contribute to insulin resistance. AMP-activated protein kinase (AMPK) regulates nutrient metabolism and is reported to have anti-inflammatory actions in adipose tissue, yet the mechanisms underlying this remain poorly characterised. The effect of AMPK activation on cytokine-stimulated proinflammatory signalling was therefore assessed in cultured adipocytes. AMPK activation inhibited IL-1β-stimulated CXCL10 secretion, associated with reduced interleukin-1 receptor associated kinase-4 (IRAK4) phosphorylation and downregulated MKK4/JNK and IKK/IκB/NFκB signalling. AMPK activation inhibited TNF-α-stimulated IKK/IκB/NFκB signalling but had no effect on JNK phosphorylation. The JAK/STAT3 pathway was also suppressed by AMPK after IL-6 stimulation and during adipogenesis. Adipose tissue from AMPKα1-/- mice exhibited increased JNK and STAT3 phosphorylation, supporting suppression of these distinct proinflammatory pathways by AMPK in vivo. The inhibition of multiple pro-inflammatory signalling pathways by AMPK may underlie the reported beneficial effects of AMPK activation in adipose tissue.

Keywords: AMP-activated protein kinase; Adipocyte; Inflammation; Signalling.

MeSH terms

  • 3T3-L1 Cells
  • AMP-Activated Protein Kinases / metabolism*
  • Adipocytes / enzymology*
  • Adipocytes / pathology*
  • Adipogenesis / drug effects
  • Animals
  • Biphenyl Compounds
  • Chemokine CXCL10 / genetics
  • Chemokine CXCL10 / metabolism
  • Enzyme Activation / drug effects
  • Female
  • Humans
  • Inflammation / enzymology*
  • Inflammation / pathology*
  • Interleukin-1 Receptor-Associated Kinases / metabolism*
  • Interleukin-1beta / metabolism
  • Interleukin-6 / metabolism
  • Mice
  • NF-kappa B / metabolism
  • Phosphorylation / drug effects
  • Pyrones / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Interleukin-6 / metabolism
  • STAT3 Transcription Factor / metabolism
  • Thiophenes / pharmacology

Substances

  • Biphenyl Compounds
  • CXCL10 protein, human
  • Chemokine CXCL10
  • Interleukin-1beta
  • Interleukin-6
  • NF-kappa B
  • Pyrones
  • RNA, Messenger
  • Receptors, Interleukin-6
  • STAT3 Transcription Factor
  • Thiophenes
  • Interleukin-1 Receptor-Associated Kinases
  • AMP-Activated Protein Kinases
  • 4-hydroxy-3-(4-(2-hydroxyphenyl)phenyl)-6-oxo-7H-thieno(2,3-b)pyridine-5-carbonitrile