The effects of inflammatory cytokines on steroidogenic acute regulatory protein expression in macrophages

Inflamm Res. 2007 Dec;56(12):495-501. doi: 10.1007/s00011-007-6133-3.

Abstract

Objective: To investigate the expression of steroidogenic acute regulatory protein (StAR) in macrophages and the effects of inflammatory cytokines on StAR expression.

Methods: The macrophages isolated from ApoE knockout mice and C57BL/6J mice and RAW264.7 cells (a cell line from mouse macrophage. ATCC Number: TIB-71) were cultured in DMEM containing 10% fetal bovine serum. RAW264.7 cells were treated with different inflammatory cytokines (TNF-alpha, IFN-gamma and TGF-beta1) and 8-Br-cAMP, a cAMP analog. RT-PCR and Western blot analysis were applied to evaluate the effects of inflammatory cytokines on StAR expression.

Results: RT-PCR and Western blot analysis demonstrated the expression of StAR in the macrophages isolated from ApoE knockout mice, C57BL/6J mice and RAW264.7 cells. Proinflammatory cytokines TNF-alpha and IFN-gamma significantly decreased StAR mRNA and protein levels in RAW264.7 cells. The inhibition was dose- and time-dependent. In contrast, anti-inflammatory cytokine TGF-beta1 increased StAR mRNA and protein levels. At 1:15 molecular ratio, TGF-beta1 blocked the down-regulation of StAR expression mediated by TNF-alpha. cAMP also induced StAR expression in RAW264.7 cells. When the cells were co-treated with 8-Br-cAMP and TNF-alpha, 8-Br-cAMP failed to induce StAR expression.

Conclusion: Our results provide interesting evidence that inflammatory cytokines regulate StAR expression in macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Bromo Cyclic Adenosine Monophosphate / pharmacology
  • Animals
  • Apolipoproteins E / genetics
  • Cell Line
  • Cyclic AMP / metabolism
  • Cytokines / pharmacology*
  • Cytokines / physiology
  • Gene Expression Regulation
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phosphoproteins / biosynthesis*
  • Phosphoproteins / genetics
  • RNA, Messenger / biosynthesis
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Apolipoproteins E
  • Cytokines
  • Phosphoproteins
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • steroidogenic acute regulatory protein
  • 8-Bromo Cyclic Adenosine Monophosphate
  • Cyclic AMP