Effects of cartilage-derived morphogenetic protein-3 on the expression of chondrogenic and osteoblastic markers in the pluripotent mesenchymal C3H10T1/2 cell line

Growth Factors. 2010 Apr;28(2):117-28. doi: 10.3109/08977190903512586.

Abstract

CDMP-3/GDF-7/BMP-12 treatment of pluripotent mesenchymal C3H10T1/2 cells resulted in a dose- and time-dependent change in cell morphology and in the expression of alkaline phosphatase, mRNA expression of osteocalcin, and bone sialoprotein, as well as mineralized bone nodule formation. CDMP-3 also stimulated Alcian Blue staining indicative of extracellular matrix formation without affecting aggrecan expression. CDMP-3 downregulated mRNA expression of BMP-4 and BMP-8A. CDMP-3 stimulated mRNA expression of ALK-1, ALK-2(ActR-IA), ALK-3(BMPR-IA), and ALK-4 without affecting that of ALK-6(BMPR-IB), ALK-7, and BMPR-II. These findings suggest that, under the experimental conditions studied, CDMP-3 induces the pluripotent mesenchymal C3H10T1/2 cells to express both chondrocytic and osteoblastic markers. The results further reveal potential complex interplay between the different bone morphogenetic proteins and their receptors in these processes.

MeSH terms

  • Animals
  • Bone Morphogenetic Proteins / metabolism*
  • Bone Morphogenetic Proteins / pharmacology
  • Cartilage / cytology*
  • Cartilage / drug effects
  • Cartilage / metabolism
  • Cell Differentiation / drug effects*
  • Cell Line
  • Chondrogenesis / drug effects
  • Gene Expression Regulation / drug effects*
  • Gene Expression Regulation / physiology
  • Growth Differentiation Factors / metabolism*
  • Growth Differentiation Factors / pharmacology
  • Mesoderm / cytology
  • Mesoderm / physiology
  • Mice
  • Osteoblasts / cytology*

Substances

  • Bone Morphogenetic Proteins
  • GDF7 protein, human
  • Growth Differentiation Factors