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Effect of extracellular matrix proteins on vascular smooth muscle cell phenotype
Authors:I. P. Hayward  K. R. Bridle  G. R. Campbell  P. A. Underwood  J. H. Campbell
Affiliation:1. Biochemistry Department, Iran University of Medical Sciences, Tehran, Iran;2. Medicine Biochemistry, Qom Branch, Islamic Azad University, Qom, Iran;3. Biochemistry Department, Tarbiat Modares University of Medical Sciences, Tehran, Iran;4. Shahid Rajaee Hospital, Iran University of Medical Sciences, Tehran, Iran;5. Microbial Biotechnology Research Center, Biochemistry Department, Iran University of Medical Sciences, Tehran, Iran;6. Student Research Committee, Iran University of Medical Sciences, Tehran, Iran
Abstract:The effect on phenotypic expression of rabbit vascular smooth muscle cells (SMC) of the interstitial matrix proteins collagen I and fibronectin, the basal lamina proteins collagen IV and laminin, and the serum adhesion protein vitronectin was examined in culture. Experiments were performed in foetal calf serum stripped of fibronectin and vitronectin to eliminate their confounding effects. All the proteins promoted adhesion to the plastic culture dish (in a concentration dependent manner) of SMC freshly isolated from the artery wall. These cells had a high volume density of myofilaments (Vvmyo) in their cytoplasm. Laminin was best at maintaining SMC with a high Vvmyo (Vvmyo = 49.8%) followed by collagen IV (41.7%). Cells plated on vitronectin showed the lowest Vvmyo (31.3%). The results support the concept that the SMC basal lamina has a role in maintaining cells in the high Vvmyo phenotype.
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