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Vascular smooth muscle cell differentiation-2010

Vascular smooth muscle cell differentiation–2010
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摘要 Vascular smooth muscle cells have attracted considerable interest as a model for a flexible program of gene expression.This cell type arises throughout the embryo body plan via poorly understood signaling cascades that direct the expression of transcription factors and microRNAs which,in turn,orchestrate the activation of contractile genes collectively defining this cell lineage.The discovery of myocardin and its close association with serum response factor has represented a major break-through for the molecular understanding of vascular smooth muscle cell differentiation.Retinoids have been shown to improve the outcome of vessel wall remodeling following injury and have provided further insights into the molecular circuitry that defines the vascular smooth muscle cell phenotype.This review summarizes the progress to date in each of these areas of vascular smooth muscle cell biology. Vascular smooth muscle cells have attracted considerable interest as a model for a flexible program of gene expression.This cell type arises throughout the embryo body plan via poorly understood signaling cascades that direct the expression of transcription factors and microRNAs which,in turn,orchestrate the activation of contractile genes collectively defining this cell lineage.The discovery of myocardin and its close association with serum response factor has represented a major break-through for the molecular understanding of vascular smooth muscle cell differentiation.Retinoids have been shown to improve the outcome of vessel wall remodeling following injury and have provided further insights into the molecular circuitry that defines the vascular smooth muscle cell phenotype.This review summarizes the progress to date in each of these areas of vascular smooth muscle cell biology.
出处 《The Journal of Biomedical Research》 CAS 2010年第3期169-180,共12页 生物医学研究杂志(英文版)
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  • 1Yang ZY , Simari RD, Perkins ND , et al. Role of the p21Cyclin-dependent kinase inhibitor in limiting intimal cell proliferation in response to arterial injury. Proc Natl Acad Sci USA, 1996,93 (15) : 7905-7910
  • 2Guo K, Andres V, Walsh K, et al. Nitric Oxide-induced downregulation of cdk2 activity and CyclinA gene transcription in vascular smooth muscle cells. Circulation, 1998; 97(20):2066-2072
  • 3Sylvester AM, Chen D, Krasinsky K, et al. Role of c-fos and E2F in the induction of cyclinA transcription and vascular smooth muscle cell proliferation. J Clin Invest, 1998;101(5):940-948
  • 4Yoshizumi M , Hsieh CM , Zhou F , et al. The ATF site med iates downregulation of the cyclinA gene during contact inhibition in vascular endothelial cells. Mol Cell Biol, 1995;15(6) :3266-3272
  • 5Boyle JO. Retinoid mechanisms and cyclins. Curr Oncol Rep,2001;3(4):301-305
  • 6Takatsuka J, Takahashi N, DelucalM. Retinoic acid metabolism and inhibition of cell proliferation:an unexpected liaison. Cancer Res, 1996;56(4):675-678
  • 7Miano JM, Topouzis S, Majesky MW, et al. Retinoid receptor expression and all trans-retinoic acid mediated growth inhibition in vascular smooth muscle cells. Circulation, 1996;93(4):1886-1895
  • 8司徒振强 吴军正.细胞培养[M].西安:世界图书出版公司西安公司,1996.68-79.

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