Proliferation of smooth muscle cells (SMC) in the arterial intima of man and experimental animals is important in the pathogenesis of atherosclerosis. Vascular SMC proliferation in vitro is stimulated by a number of agents, including the potent protein mitogen, platelet-derived growth factor (PDGF).
Human iliac artery endothelial cells express both genes encoding the chains of platelet-derived growth factor (PDGF) and synthesize PDGF-like mitogen
โ Scribed by N. M. Sitaras; E. Sariban; P. Pantazis; B. Zetter; H. N. Antoniades
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 552 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0021-9541
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โฆ Synopsis
In human umbilical vein and bovine aortic endothelial cells in culture c-sis gene expression and secretion of platelet-derived growth factor (PDGF) has been previously demonstrated. We now report the presence of PDGF-1 and PDGF-Z/sis mRNA transcripts in primary cultures of human iliac artery endothelial cells (HIA-EC). Concomitantly, these cells synthesize and secrete PDGFlike proteins identified by direct irnmunoprecipitation with specific PDGF antiserum. T h e PDCF proteins secreted by HIA-EC have molecular weights of 31 and 35 kd under nonreducing conditions. Upon reduction these proteins are converted to the monomeric 15-and 16-kd forms. Conditioned media derived from HIA-EC stimulated the incorporation of 3H-thymidine by 3T3 cells and competed with 1251-PDCF for its binding to 3T3 cell membrane receptors. The biologic activity was stable to heating at 100ยฐC for 10 min and sensitive to reducing agents, properties similar to those of authentic PDGF. Production of PDGF-like mitogen by the human arterial endothelial cells may play an important role in the paracrine modulation of arterial wall regeneration following vascular injury.
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