1. Academic Validation
  2. Adipocyte lipolysis-stimulated interleukin-6 production requires sphingosine kinase 1 activity

Adipocyte lipolysis-stimulated interleukin-6 production requires sphingosine kinase 1 activity

  • J Biol Chem. 2014 Nov 14;289(46):32178-32185. doi: 10.1074/jbc.M114.601096.
Wenliang Zhang 1 Emilio P Mottillo 2 Jiawei Zhao 1 Allison Gartung 1 Garrett C VanHecke 3 Jen-Fu Lee 1 Krishna R Maddipati 1 Haiyan Xu 4 Young-Hoon Ahn 3 Richard L Proia 5 James G Granneman 6 Menq-Jer Lee 7
Affiliations

Affiliations

  • 1 Departments of Pathology, Wayne State University, Detroit, Michigan 48202; Departments of Bioactive Lipid Research Program, Wayne State University, Detroit, Michigan 48202.
  • 2 Departments of Pathology, Wayne State University, Detroit, Michigan 48202; Center for Integrative Metabolic and Endocrine Research, Wayne State University, Detroit, Michigan 48202.
  • 3 Department of Chemistry, Wayne State University, Detroit, Michigan 48202.
  • 4 Department of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island 02912, and.
  • 5 Genetics of Development and Disease Branch, NIDDK, National Institutes of Health, Bethesda, Maryland 20814.
  • 6 Departments of Pathology, Wayne State University, Detroit, Michigan 48202; Center for Integrative Metabolic and Endocrine Research, Wayne State University, Detroit, Michigan 48202; Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48202. Electronic address: [email protected].
  • 7 Departments of Pathology, Wayne State University, Detroit, Michigan 48202; Departments of Bioactive Lipid Research Program, Wayne State University, Detroit, Michigan 48202; Karmanos Cancer Institute, and Wayne State University, Detroit, Michigan 48202; Cardiovascular Research Institute, Wayne State University, Detroit, Michigan 48202,. Electronic address: [email protected].
Abstract

Adipocyte lipolysis can increase the production of inflammatory cytokines such as interleukin-6 (IL-6) that promote Insulin resistance. However, the mechanisms that link lipolysis with inflammation remain elusive. Acute activation of β3-adrenergic receptors (ADRB3) triggers lipolysis and up-regulates production of IL-6 in adipocytes, and both of these effects are blocked by pharmacological inhibition of hormone-sensitive Lipase. We report that stimulation of ADRB3 induces expression of sphingosine kinase 1 (SphK1) and increases sphingosine 1-phosphate production in adipocytes in a manner that also depends on hormone-sensitive Lipase activity. Mechanistically, we found that adipose lipolysis-induced SphK1 up-regulation is mediated by the c-Jun N-terminal kinase (JNK)/activating protein-1 signaling pathway. Inhibition of SphK1 by sphingosine kinase inhibitor 2 diminished the ADRB3-induced IL-6 production both in vitro and in vivo. Induction of IL-6 by ADRB3 activation was suppressed by siRNA knockdown of Sphk1 in cultured adipocytes and was severely attenuated in Sphk1 null mice. Conversely, ectopic expression of SphK1 increased IL-6 expression in adipocytes. Collectively, these data demonstrate that SphK1 is a critical mediator in lipolysis-triggered inflammation in adipocytes.

Keywords

AP1 Transcription Factor (AP-1); Adipose Tissue; Beta 3 Adrenergic Receptor; Hormone-sensitive Lipase; Inflammation; Interleukin 6 (IL-6); Lipolysis; Sphingosine Kinase; c-Jun N-terminal Kinase (JNK).

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