Literature DB >> 9650223

The role of the extracellular matrix in arterial remodelling.

W D Coats1, D P Faxon.   

Abstract

The extracellular matrix is now recognized as a biologically active and dynamic composition of structural, adhesive, and counteradhesive fibrous proteins embedded in a hydrated ground substance of glycosaminoglycans and proteoglycans. The ability of resident cells to detect small differences in the specific combination, concentration and distribution of matrix components suggests that perturbation of the homeostatic matrix can lead to remodelling following angioplasty. Recent studies reviewed herein have focused on how alterations of the relative composition of matrix components ultimately leads to changes in cell growth, behaviour and differentiation, all of which can significantly contribute to remodelling of the vascular wall following injury. These cell-matrix interactions may provide novel therapeutic targets in the prevention of unfavourable remodelling that leads to restenosis.

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Year:  1997        PMID: 9650223

Source DB:  PubMed          Journal:  Semin Interv Cardiol        ISSN: 1084-2764


  4 in total

Review 1.  The mechanisms of coronary restenosis: insights from experimental models.

Authors:  G A Ferns; T Y Avades
Journal:  Int J Exp Pathol       Date:  2000-04       Impact factor: 1.925

2.  Atorvastatin calcium inhibits phenotypic modulation of PDGF-BB-induced VSMCs via down-regulation the Akt signaling pathway.

Authors:  Shuang Chen; Baoqin Liu; Dehui Kong; Si Li; Chao Li; Huaqin Wang; Yingxian Sun
Journal:  PLoS One       Date:  2015-04-15       Impact factor: 3.240

3.  Resveratrol inhibits phenotype modulation by platelet derived growth factor-bb in rat aortic smooth muscle cells.

Authors:  Mi Hee Lee; Byeong-Ju Kwon; Hyok Jin Seo; Kyeong Eun Yoo; Min Sung Kim; Min-Ah Koo; Jong-Chul Park
Journal:  Oxid Med Cell Longev       Date:  2014-03-10       Impact factor: 6.543

4.  Mitogenesis of vascular smooth muscle cell stimulated by platelet-derived growth factor-bb is inhibited by blocking of intracellular signaling by epigallocatechin-3-O-gallate.

Authors:  Mi Hee Lee; Byeong-Ju Kwon; Min-Ah Koo; Kyung Eun You; Jong-Chul Park
Journal:  Oxid Med Cell Longev       Date:  2013-11-06       Impact factor: 6.543

  4 in total

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