(Circulation. 1999;100:855-860.)
© 1999 American Heart Association, Inc.
Basic Science Reports |
From Institut für Kardiovaskuläre Physiologie, Klinikum der JWG-Universität (N.K., A.B., R.B., V.B.S.-K.), Frankfurt am Main and Fachbereich Hämostaseologie, Stiftung Deutsche Klinik für Diagnostik GmbH (S.B., C.M.K.), Wiesbaden, Germany.
Correspondence to V.B. Schini-Kerth, PhD, Institut für Kardiovaskuläre Physiologie, Klinikum der JWG-Universität, Theodor-Stern-Kai-7, D-60590 Frankfurt am Main, Germany. E-mail Schini-Kerth{at}em.uni-frankfurt.de
BackgroundVascular endothelial growth factor (VEGF), an endothelial mitogen and chemoattractant, has been implicated in the recovery of the endothelium after balloon injury. The increased expression of VEGF in vascular smooth muscle cells (SMC) at sites of injury suggests that this cell type may be a major cellular source of VEGF. This study examined whether aggregating platelets stimulate VEGF expression in cultured SMC.
Methods and ResultsVEGF expression in SMC was assessed by Northern blot analysis and by reverse transcription followed by polymerase chain reaction and the release of VEGF by Western blot analysis and immunoassay. Platelet-derived products (PDP) released by aggregating human platelets time-dependently and concentration-dependently enhanced VEGF mRNA levels, mainly that coding for the soluble splice variant VEGF165/164, and stimulated the release of VEGF protein. These effects were potentiated by transient acidification of PDP, which release bioactive transforming growth factor (TGF)-ß1, and mimicked by platelet-derived growth factor (PDGF)AB and TGF-ß1 in a synergistic manner. Both a TGF-ßneutralizing antibody and a PDGF-neutralizing antibody significantly attenuated the effect of acidified PDP on VEGF production.
ConclusionsAggregating human platelets induce VEGF mRNA expression in cultured SMC and the subsequent release of VEGF protein. This effect can be attributed to a supra-additive action of PDGFAB and TGF-ß1 and may represent a novel mechanism by which platelets contribute to the recovery of the endothelial lining at sites of balloon-injured arteries.
Key Words: platelet-derived factors angiogenesis muscle, smooth arteriosclerosis
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