Transient expression of M-CSF is important for osteoclast-like cell differentiation in a monocytic leukemia cell line

J Cell Biochem. 1997 Jan;64(1):67-76. doi: 10.1002/(sici)1097-4644(199701)64:1<67::aid-jcb10>3.0.co;2-h.

Abstract

Cells of U937, a human monocytic leukemia cell line, differentiate into macrophages by treatment with 12-o-tetradecanoylphorbol-13-acetate (TPA), whereas cells treated with 1 alpha, 25-dihydroxyvitamin D3 [1,25-(OH)2D3] continue to grow without undergoing differentiation. When U937 cells were successively treated with TPA and 1,25-(OH)2D3, tartrate-resistant acid phosphatase-positive multinucleated cells appeared at 5 days after the treatment. These osteoclast-like cells released a soluble form of 45Ca from 45Ca-labeled bone particles. These cells were not formed when the order of treatment with TPA and 1,25-(OH)2D3 was reversed. Use of either dexamethasone or interferon-gamma (IFN-gamma) was effective in inhibiting the formation of these osteoclast-like cells. The expression of c-src, c-fms, and macrophage colony stimulating factor (M-CSF) was induced by TPA treatment; however, TPA-induced M-CSF gene transcription was attenuated by the subsequent addition of 1,25-(OH)2D3. Furthermore, both dexamethasone and IFN-gamma impaired the attenuation of M-CSF expression, suggesting that the transient expression of M-CSF may be important for the formation of osteoclast-like cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acid Phosphatase / pharmacology
  • Animals
  • Calcitonin / pharmacology
  • Calcitriol / pharmacology
  • Carcinogens / pharmacology
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics
  • Cell Nucleus / drug effects
  • Dexamethasone / pharmacology
  • Diterpenes*
  • Drug Synergism
  • Gene Expression Regulation, Leukemic / drug effects*
  • Genes, fms
  • Genes, src
  • Humans
  • Interferon-gamma / pharmacology
  • Isoenzymes / pharmacology
  • Leukemia, Monocytic, Acute / drug therapy
  • Leukemia, Monocytic, Acute / genetics
  • Leukemia, Monocytic, Acute / pathology*
  • Macrophage Colony-Stimulating Factor / drug effects
  • Macrophage Colony-Stimulating Factor / genetics*
  • Mice
  • Osteoclasts / drug effects
  • Osteoclasts / pathology*
  • Phenotype
  • Tartrate-Resistant Acid Phosphatase
  • Terpenes / pharmacology
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Carcinogens
  • Diterpenes
  • Isoenzymes
  • Terpenes
  • mezerein
  • Dexamethasone
  • Macrophage Colony-Stimulating Factor
  • Interferon-gamma
  • Calcitonin
  • Acid Phosphatase
  • Tartrate-Resistant Acid Phosphatase
  • Calcitriol
  • Tetradecanoylphorbol Acetate