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PDGF stimulates DNA synthesis in human vascular smooth muscle cells via a novel wortmannin-insensitive phosphatidylinositol 3-kinase
Authors:Lymn Joanne S  Gallagher Karen L  Clunn Gerard F  Fexby Sofi E  Patel Mahendra K  Hughes Alun D
Affiliation:Clinical Pharmacology, Imperial College Faculty of Medicine, National Heart and Lung Institute, St Mary's Campus, Paddington, London W2 1NY, UK. j.lymn@imperial.ac.uk
Abstract:
The class 1(A) phosphatidylinositol 3-kinase enzymes consist of a number of heterodimeric complexes of regulatory and catalytic subunits and have been implicated in a number of cellular responses. While platelet-derived growth factor (PDGF)-induced chemotaxis of human vascular smooth muscle cells (HVSMC) is inhibited by both wortmannin and LY294002, DNA synthesis is only inhibited by LY294002. Serum-induced DNA synthesis however is inhibited by LY294002, wortmannin and rapamycin. Similarly PDGF-induced protein kinase B (PKB) activation is inhibited by LY294002 but not by wortmannin or rapamycin. In conclusion PDGF-induced DNA synthesis appears to occur through a phosphatidylinositol 3-kinase (PI3-K)-dependent, but wortmannin-insensitive, PKB/Akt pathway.
Keywords:Platelet-derived growth factor   Vascular smooth muscle   DNA synthesis   Phosphatidylinositol 3-kinase
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