Activated human T lymphocytes express cyclooxygenase-2 and produce proadipogenic prostaglandins that drive human orbital fibroblast differentiation to adipocytes

Am J Pathol. 2006 Oct;169(4):1183-93. doi: 10.2353/ajpath.2006.060434.

Abstract

The differentiation of preadipocyte fibroblasts to adipocytes is a crucial process to many disease states including obesity, cardiovascular, and autoimmune diseases. In Graves' disease, the orbit of the eye can become severely inflamed and infiltrated with T lymphocytes as part of the autoimmune process. The orbital fibroblasts convert to fat-like cells causing the eye to protrude, which is disfiguring and can lead to blindness. Recently, the transcription factor peroxisome proliferator activated receptor (PPAR)-gamma and its natural (15d-PGJ2) and synthetic (thiazolidinedione-type) PPAR-gamma agonists have been shown to be crucial to the in vitro differentiation of preadipocyte fibroblasts to adipocytes. We show herein several novel findings. First, that activated T lymphocytes from Graves' patients drive the differentiation of PPAR-gamma-expressing orbital fibroblasts to adipocytes. Second, this adipogenic differentiation is blocked by nonselective small molecule cyclooxygenase (Cox)-1/Cox-2 inhibitors and by Cox-2 selective inhibitors. Third, activated, but not naïve, human T cells highly express Cox-2 and synthesize prostaglandin D2 and related prostaglandins that are PPAR-gamma ligands. These provocative new findings provide evidence for how activated T lymphocytes, through production of PPAR-gamma ligands, profoundly influence human fibroblast differentiation to adipocytes. They also suggest the possibility that, in addition to the orbit, T lymphocytes influence the deposition of fat in other tissues.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology*
  • Adipogenesis*
  • Cell Differentiation*
  • Coculture Techniques
  • Cyclooxygenase 2 / metabolism*
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • Graves Disease / enzymology
  • Humans
  • Ligands
  • Lymphocyte Activation
  • Membrane Proteins / metabolism*
  • Orbit / cytology*
  • PPAR gamma / agonists
  • PPAR gamma / metabolism
  • Prostaglandin D2 / analogs & derivatives
  • Prostaglandin D2 / biosynthesis
  • Prostaglandin D2 / pharmacology
  • Prostaglandins / biosynthesis*
  • T-Lymphocytes / enzymology*
  • T-Lymphocytes / metabolism

Substances

  • 15-deoxyprostaglandin J2
  • Ligands
  • Membrane Proteins
  • PPAR gamma
  • Prostaglandins
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin D2