Cyclooxygenase-2 overexpression inhibits platelet-derived growth factor-induced mesangial cell proliferation through induction of the tumor suppressor gene p53 and the cyclin-dependent kinase inhibitors p21waf-1/cip-1 and p27kip-1

J Biol Chem. 2002 Mar 22;277(12):9763-71. doi: 10.1074/jbc.M106307200. Epub 2001 Dec 26.

Abstract

Cyclooxygenase-2 (COX-2) is an inducible enzyme and serves as a source of paracrine prostaglandin E2 (PGE2) formation in many tissues. In glomerular immune injury COX-2 formation is up-regulated in association with increased mesangial cell growth. To examine whether COX-2 exerts growth modulating effects on glomerular cells, we established two separate COX-2-overexpressing mesangial cell lines (COX-2+) and assessed their proliferative response to the potent mesangial cell growth-promoting factor, platelet-derived growth factor (PDGF). PDGF increased proliferation in mock-transfected cells. In contrast, PDGF did not induce proliferation in COX-2+ cells. Our results also showed that the tumor suppressor protein p53 and the cyclin-dependent kinase inhibitors p21(cip-1) and p27(kip-1) were up-regulated in COX-2+ cells de novo as well as under PDGF-stimulated conditions. To study whether COX-2 products are required for these effects, COX-2+ cells were treated with indomethacin (1 microg/ml) or NS-398 (3 microm). Unexpectedly, both COX inhibitors had no significant effect on cell proliferation, not on the protein levels of p53, p21(cip-1), or p27(kip-1). To evaluate the role of p21(cip-1) and p27(kip-1), COX-2 was overexpressed in mesangial cells derived from p21(cip-1) (p21-/- COX-2+) and p27(kip-1) (p27-/- COX-2+) null mice. In contrast to the wild type COX-2+ cells, p21-/- COX-2+ and p27-/- COX-2+ cells proliferated in response to PDGF. These data suggest that COX-2 inhibits mesangial cell proliferation by a novel mechanism that is independent of prostaglandin synthesis, but involves p53, p21(cip-1), and p27(kip-1).

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Cell Division
  • Cell Line
  • Cell Separation
  • Cells, Cultured
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclins / genetics
  • Cyclins / metabolism*
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / pharmacology
  • Desmin / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Genes, p53 / genetics
  • Glomerular Mesangium / cytology
  • Glomerular Mesangium / enzymology*
  • Indomethacin / pharmacology
  • Isoenzymes / biosynthesis*
  • Male
  • Nitrobenzenes / pharmacology
  • Plasmids / metabolism
  • Platelet-Derived Growth Factor / metabolism*
  • Prostaglandin-Endoperoxide Synthases / biosynthesis*
  • Prostaglandins / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Sulfonamides / pharmacology
  • Time Factors
  • Transcriptional Activation
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism*
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Cdkn1a protein, rat
  • Cdkn1b protein, rat
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Desmin
  • Isoenzymes
  • Nitrobenzenes
  • Platelet-Derived Growth Factor
  • Prostaglandins
  • Sulfonamides
  • Tumor Suppressor Protein p53
  • Tumor Suppressor Proteins
  • N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Indomethacin