Regulation of transforming growth factor-beta-dependent cyclooxygenase-2 expression in fibroblasts

J Biol Chem. 2009 Dec 18;284(51):35861-71. doi: 10.1074/jbc.M109.014639.

Abstract

Abnormal transforming growth factor-beta (TGF-beta) signaling is a critical contributor to the pathogenesis of various human diseases ranging from tissue fibrosis to tumor formation. Excessive TGF-beta signaling stimulates fibrotic responses. Recent research has focused in the main on the antiproliferative effects of TGF-beta in fibroblasts, and it is presently understood that TGF-beta-stimulated cyclooxygenase-2 (COX-2) induction in fibroblasts is essential for antifibroproliferative effects of TGF-beta. Both TGF-beta and COX-2 have been implicated in tumor growth, invasion, and metastasis, and therefore tumor-associated fibroblasts are a recent topic of interest. Here we report the identification of positive and negative regulatory factors of COX-2 expression induced by TGF-beta as determined using proteomic approaches. We show that TGF-beta coordinately up-regulates three factors, heterogeneous nuclear ribonucleoprotein A/B (HNRPAB), nucleotide diphosphate kinase A (NDPK A), and nucleotide diphosphate kinase A (NDPK B). Functional pathway analysis showed that HNRPAB augments mRNA and protein levels of COX-2 and subsequent prostaglandin E(2) (PGE(2)) production by suppressing degradation of COX-2 mRNA. In contrast, NDPK A and NDPK B attenuated mRNA and protein levels of COX-2 by affecting TGF-beta-Smad2/3/4 signaling at the receptor level. Collectively, we report on a new regulatory pathway of TGF-beta in controlling expression of COX-2 in fibroblasts, which advances our understanding of pathophysiological mechanisms of TGF-beta.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cyclooxygenase 2 / biosynthesis*
  • Dinoprostone / biosynthesis
  • Fibroblasts / cytology
  • Fibroblasts / enzymology*
  • Gene Expression Regulation, Enzymologic / drug effects
  • Gene Expression Regulation, Enzymologic / physiology*
  • Heterogeneous-Nuclear Ribonucleoprotein Group A-B / metabolism
  • Humans
  • Mice
  • NM23 Nucleoside Diphosphate Kinases / metabolism
  • RNA, Messenger / biosynthesis
  • Repressor Proteins / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Smad Proteins / metabolism
  • Transforming Growth Factor beta1 / metabolism*
  • Transforming Growth Factor beta1 / pharmacology
  • Up-Regulation / drug effects
  • Up-Regulation / physiology

Substances

  • Heterogeneous-Nuclear Ribonucleoprotein Group A-B
  • NM23 Nucleoside Diphosphate Kinases
  • RNA, Messenger
  • Repressor Proteins
  • Smad Proteins
  • Transforming Growth Factor beta1
  • Hnrnpab protein, mouse
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Nme1 protein, mouse
  • Dinoprostone