Recombinant human bone morphogenetic protein-2 induces osteoblastic differentiation in W-20-17 stromal cells

Endocrinology. 1992 Mar;130(3):1318-24. doi: 10.1210/endo.130.3.1311236.

Abstract

To better understand the in vivo bone-inductive properties of recombinant human (rh) BMP-2, we examined the ability of the protein to alter the phenotype of a bone marrow stromal cell line. W-20-17. rhBMP-2 increased alkaline phosphatase activity in W-20-17 cells in a dose-responsive manner in the absence of an effect on proliferation. The induction of alkaline phosphatase activity was not apparent until 12 h after rhBMP-2 treatment had begun and was effectively eliminated by cotreatment with cycloheximide, suggesting a requirement for protein synthesis. Continued treatment of W-20-17 cells with rhBMP-2 for 8 days resulted in a significant increase, compared to control cultures, in the production of cellular cAMP in response to a PTH challenge. In addition, 4-day treatment with rhBMP-2 induced osteocalcin levels in W-20-17 cells. These results indicate that rhBMP-2 induces the expression of several markers associated with the osteoblast phenotype in W-20-17 cells and raises the possibility that BMP-2 may be involved in the differentiation of osteoblasts from progenitor cells resident in bone marrow.

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Animals
  • Blotting, Northern
  • Bone Morphogenetic Proteins
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Cyclic AMP / metabolism
  • Cycloheximide / pharmacology
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Enzyme Activation / drug effects
  • Humans
  • Mice
  • Osteoblasts / cytology*
  • Osteoblasts / drug effects
  • Osteoblasts / metabolism
  • Osteocalcin / metabolism
  • Parathyroid Hormone / pharmacology
  • Phenotype
  • Proteins / pharmacology*
  • Recombinant Proteins / pharmacology
  • Thymidine / metabolism
  • Tritium

Substances

  • Bone Morphogenetic Proteins
  • Parathyroid Hormone
  • Proteins
  • Recombinant Proteins
  • Tritium
  • Osteocalcin
  • DNA
  • Cycloheximide
  • Cyclic AMP
  • Alkaline Phosphatase
  • Thymidine