Functional genomics of PPAR-gamma in human immunomodulatory cells

Mol Cell Biochem. 2006 Oct;290(1-2):211-5. doi: 10.1007/s11010-006-9169-8. Epub 2006 Apr 22.

Abstract

Keeping in view the fact that peroxisome-proliferators activated receptors-PPARs (alpha,gamma) play a crucial role in atherogenic inflammation, the present study was addressed to explore as to how selective and specific PPAR-gamma gene silencing within human mononuclear cells affects genes involved in lipid metabolism and innate immune process. Such a study revealed that with respect to control cells, the PPAR-gamma knock-out cells exhibited significant reduction in the expression of genes coding for PPAR- alpha, CD-36, LDL-R as well as significant increase in the expression of genes coding for IL-4, IL-8, IFN-gamma, CX3CR1, hTERT. However, the expression of genes coding for LXR-alpha and Receptor-C( k ) could not be detected in PPAR-gamma knock-out cells. Based on these results, we propose that PPAR-gamma gene has the inherent capacity to influence the lipid mediated inflammation process in atherosclerotic lesions.

MeSH terms

  • Cells, Cultured
  • Genomics*
  • Humans
  • Immunity, Innate / genetics*
  • Inflammation / genetics
  • Lipid Metabolism / genetics
  • PPAR gamma / blood
  • PPAR gamma / genetics*
  • PPAR gamma / physiology*
  • RNA, Messenger / metabolism*
  • RNA, Small Interfering
  • Transfection

Substances

  • PPAR gamma
  • RNA, Messenger
  • RNA, Small Interfering