Journal
JOURNAL OF CELLULAR PHYSIOLOGY
Volume 217, Issue 1, Pages 48-59Publisher
WILEY-LISS
DOI: 10.1002/jcp.21471
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Funding
- PRIN 2005, Italy
- Fondazione Carima, Italy
- NIH [AG021189]
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The present investigation extends our previous studies on PGF2 alpha-mediated signalling in osteoblast metabolism. In particular, the role of PGF2 alpha as modulator of heparan sulphate proteoglycans (HSPGs), fibroblast growth factor 2 (FGF-2) and fibroblast growth factor receptors (FGFRs) was evaluated. We hereby reported the novel observation that PGF2 alpha was able to promote the formation of HSPGs/ FGF-2/FGFRs complexes. Moreover, our data suggested that PGF2a could induce new synthesis of heparan sulphate (HS) chains on osteoblasts by a mechanism involving a modulation of MAPK signalling and that HS is required for the regulation of FGF-2 induced by PGF2 alpha. Indeed, a proteolytic cleavage of HSPGs with heparinase III (Hep III) prior to PGF2 alpha administration down-regulated the basal expression of phospho-p44/42, likely inhibiting FGFRs tyrosine kinase activity. Interestingly, MAPK signalling influenced syntheses and subcellular localization of FGF-2, its specific receptor and HS. In addition, the proteolytic cleavage by Hep III and the MAPK kinase inhibition by PD-98059 also revealed that PGF2 alpha induced cell proliferation is dependent on HSPGs and FGF-2 specific receptor, respectively. Of further relevance of this study, we demonstrated, by using a specific siRNA for FGFR 1, that PGF2a modulates Runx2 expression by FGFR I and HS.
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