Phosphotyrosine (P-Tyr) antibodies have been used to identify the phosphorylated forms of growth factor receptors and oncogene-coded tyrosine kinases. Western blot analysis of a gastric carcinoma cell line with P-Tyr antibodies revealed a tyrosine-phosphorylated protein of M, 145,000 (P145). In addi
Studies on the autocrine activation of a synovial cell line
β Scribed by M. E. Baratz; H. I. Georgescu; Dr. C. H. Evans
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 640 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0736-0266
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The lapine synovial cell line HIGβ82 secretes factors that activate cultures of articular chondrocytes. We showed that these βchrondrocyteβactivating factorsβ (CAF) also activate quiescent cultures of HIGβ82 cells in an autocrine fashion. After exposure to partially purified preparations of CAF, HIGβ82 cells increased their synthesis of prostaglandin E~2~ (PGE~2~) and the neutral proteinases collagenase, gelatinase, and stromelysin. CAF also induced their own synthesis. Both PGE~2~ synthesis and endogenous production of CAF started to increase between 1 and 3 h after treatment of cells with exogenous CAF, but the neutral proteolytic activity of the conditioned medium took βΌ 12 h to increase. Induction of neutral proteinases by CAF was inversely related to the degree of cell confluency. Whereas their induction by phorbol myristate acetate (PMA) was independent of this parameter. Both CAF and PMA provoked morphologic changes in subconfluent cultures of HIGβ82 cells. Although the intracellular concentration of free Ca^2+^ increased rapidly in response to CAF, the results of experiments with calcium channel blockers and ionophores failed to support a role for Ca^2+^ fluxes in induction of neutral proteinases. In similar types of experiments, no evidence could be found to implicate fluxes in cyclic AMP or cyclic GMP in the induction of collagenase, gelatinase, or stromelysin. Because PMA is such a strong inducer of these enzymes, protein kinase C may be involved in signal transduction, but further work is needed to determine whether this is so.
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