Tumor necrosis factor-alpha promotes in vitro calcification of vascular cells via the cAMP pathway

Circulation. 2000 Nov 21;102(21):2636-42. doi: 10.1161/01.cir.102.21.2636.

Abstract

Background: Vascular calcification is an ectopic calcification that commonly occurs in atherosclerosis. Because tumor necrosis factor-alpha (TNF-alpha), a pleiotropic cytokine found in atherosclerotic lesions, is also a regulator of bone formation, we investigated the role of TNF-alpha in in vitro vascular calcification.

Methods and results: A cloned subpopulation of bovine aortic smooth muscle cells previously shown capable of osteoblastic differentiation was treated with TNF-alpha, and osteoblastic differentiation and mineralization were assessed. Treatment of vascular cells with TNF-alpha for 3 days induced an osteoblast-like morphology. It also enhanced both activity and mRNA expression of alkaline phosphatase, an early marker of osteoblastic differentiation. Continuous treatment with TNF-alpha for 10 days enhanced matrix mineralization as measured by radiolabeled calcium incorporation in the matrix. Pretreatment of cells with a protein kinase A-specific inhibitor, KT5720, attenuated cell morphology, the alkaline phosphatase activity, and mineralization induced by TNF-alpha. Consistent with this, the intracellular cAMP level was elevated after TNF-alpha treatment. Electrophoretic mobility shift assay demonstrated that TNF-alpha enhanced DNA binding of osteoblast specific factor (Osf2), AP1, and CREB, transcription factors that are important for osteoblastic differentiation.

Conclusions: These results suggest that TNF-alpha enhances in vitro vascular calcification by promoting osteoblastic differentiation of vascular cells through the cAMP pathway.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alkaline Phosphatase / genetics
  • Alkaline Phosphatase / metabolism
  • Animals
  • Antigens, Differentiation / metabolism
  • Bone Matrix / drug effects
  • Bone Matrix / metabolism
  • Bone Matrix / pathology
  • Calcinosis / chemically induced*
  • Calcinosis / pathology
  • Cattle
  • Cell Adhesion Molecules / metabolism
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Core Binding Factor Alpha 1 Subunit
  • Cyclic AMP / metabolism*
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Intracellular Fluid / metabolism
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism*
  • Muscle, Smooth, Vascular / pathology
  • Neoplasm Proteins*
  • Osteoblasts / drug effects
  • Osteoblasts / enzymology
  • Osteoblasts / pathology
  • RNA, Messenger / metabolism
  • Second Messenger Systems / drug effects
  • Signal Transduction / drug effects*
  • Transcription Factor AP-1 / metabolism
  • Transcription Factors / metabolism
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Antigens, Differentiation
  • Cell Adhesion Molecules
  • Core Binding Factor Alpha 1 Subunit
  • Cyclic AMP Response Element-Binding Protein
  • Neoplasm Proteins
  • RNA, Messenger
  • Transcription Factor AP-1
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • Cyclic AMP
  • Alkaline Phosphatase