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Prostaglandin F2 alpha-induced mitogenesis in MC3T3-E1 osteoblasts: role of protein kinase-C-mediated tyrosine phosphorylation.

Publication ,  Journal Article
Quarles, LD; Haupt, DM; Davidai, G; Middleton, JP
Published in: Endocrinology
April 1993

Prostaglandin F2 alpha (PGF2 alpha) stimulates DNA synthesis in osteoblasts through phospholipase-C-dependent increases in intracellular calcium and protein kinase-C (PKC) activity. We present evidence that stimulation of protein tyrosine phosphorylation by PKC is an additional component of the signaling pathways involved in PGF2 alpha-stimulated DNA synthesis in MC3T3-E1 osteoblast-like cells. Mitogenic doses of PGF2 alpha (42 nM) rapidly induced tyrosine phosphorylation of multiple substrates in these osteoblast-like cells. PGF2 alpha stimulated tyrosine phosphorylation of new proteins with apparent mol wt of 87, 80, 50, 47, 36, and 33 kilodaltons and up-regulated phosphorylation of preexisting tyrosine components with mol wt of 123, 112, 68, and 56 kilodaltons. Stimulation of PKC by 1.6 microM phorbol 12-myristate 13-acetate mimicked the pattern of PGF2 alpha-induced protein tyrosine phosphorylation, whereas PKC-deficient cells (induced by overnight pretreatment with 16 microM phorbol 12-myristate 13-acetate) were refractory to PGF2 alpha-stimulated protein tyrosine phosphorylation and DNA synthesis. The tyrosine kinase inhibitors tyrphostin and genistein blocked PGF2 alpha-stimulated DNA synthesis and protein tyrosine phosphorylation, and the tyrosine phosphatase inhibitor orthovanadate prolonged PGF2 alpha-stimulated tyrosine phosphorylation; these findings are consistent with activation of a putative tyrosine kinase. Calcium/calmodulin antagonists also inhibited PGF2 alpha-stimulated DNA synthesis, but the calcium-signaling pathway played no role in PGF2 alpha-induced tyrosine phosphorylation. Our findings suggest that cross-talk between receptor-mediated activation of PKC and protein tyrosine phosphorylation is an important distal signaling pathway necessary for PGF2 alpha-induced DNA synthesis in osteoblast-like cells.

Duke Scholars

Published In

Endocrinology

DOI

ISSN

0013-7227

Publication Date

April 1993

Volume

132

Issue

4

Start / End Page

1505 / 1513

Location

United States

Related Subject Headings

  • Tyrosine
  • Signal Transduction
  • Protein-Tyrosine Kinases
  • Protein Kinase C
  • Phosphorylation
  • Osteoblasts
  • Mitosis
  • Endocrinology & Metabolism
  • Dinoprost
  • DNA
 

Citation

APA
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MLA
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Quarles, L. D., Haupt, D. M., Davidai, G., & Middleton, J. P. (1993). Prostaglandin F2 alpha-induced mitogenesis in MC3T3-E1 osteoblasts: role of protein kinase-C-mediated tyrosine phosphorylation. Endocrinology, 132(4), 1505–1513. https://doi.org/10.1210/endo.132.4.8462449
Quarles, L. D., D. M. Haupt, G. Davidai, and J. P. Middleton. “Prostaglandin F2 alpha-induced mitogenesis in MC3T3-E1 osteoblasts: role of protein kinase-C-mediated tyrosine phosphorylation.Endocrinology 132, no. 4 (April 1993): 1505–13. https://doi.org/10.1210/endo.132.4.8462449.
Quarles LD, Haupt DM, Davidai G, Middleton JP. Prostaglandin F2 alpha-induced mitogenesis in MC3T3-E1 osteoblasts: role of protein kinase-C-mediated tyrosine phosphorylation. Endocrinology. 1993 Apr;132(4):1505–13.
Quarles, L. D., et al. “Prostaglandin F2 alpha-induced mitogenesis in MC3T3-E1 osteoblasts: role of protein kinase-C-mediated tyrosine phosphorylation.Endocrinology, vol. 132, no. 4, Apr. 1993, pp. 1505–13. Pubmed, doi:10.1210/endo.132.4.8462449.
Quarles LD, Haupt DM, Davidai G, Middleton JP. Prostaglandin F2 alpha-induced mitogenesis in MC3T3-E1 osteoblasts: role of protein kinase-C-mediated tyrosine phosphorylation. Endocrinology. 1993 Apr;132(4):1505–1513.
Journal cover image

Published In

Endocrinology

DOI

ISSN

0013-7227

Publication Date

April 1993

Volume

132

Issue

4

Start / End Page

1505 / 1513

Location

United States

Related Subject Headings

  • Tyrosine
  • Signal Transduction
  • Protein-Tyrosine Kinases
  • Protein Kinase C
  • Phosphorylation
  • Osteoblasts
  • Mitosis
  • Endocrinology & Metabolism
  • Dinoprost
  • DNA