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RGD肽对内皮细胞在聚酯材料表面粘附、增殖的影响
引用本文:武忠,石应康,赁可.RGD肽对内皮细胞在聚酯材料表面粘附、增殖的影响[J].北京生物医学工程,2003,22(4):278-280.
作者姓名:武忠  石应康  赁可
作者单位:1. 南京大学医学院附属鼓楼医院胸心外科,210008
2. 四川大学华西医院胸心外科,610041
基金项目:国家自然科学基金;29874022;
摘    要:RGD是许多粘附蛋白结构中的高度保守序列,与细胞在生物材料表面的粘附、增殖密切相关。本研究在聚酯薄膜表面分别预衬纤维粘连蛋白和共价接枝RGD三肽,然后在不同聚酯材料上种植体外培养的人脐静脉内皮细胞,结果显示RGD可明显促进细胞在材料表面的粘附和增殖,与纤维粘连蛋白相比,RGD促进细胞粘附的作用更为明显,而在细胞增殖方面,二者的作用无显著性差异。本研究为改进生物材料的表面设计,促进心血管移植物的内皮化提供了一个切实可行的思路。

关 键 词:RGD肽  内皮细胞  聚酯材料  细胞粘附  细胞增殖  生物材料  心血管移植物
文章编号:1002-3208(2003)04-0278-03
修稿时间:2003年1月6日

Effect of RGD Peptides on Endothelial Cell Adhesion and Proliferation on Polyethylene Terephthalate Surfaces
WU Zhong ,SHI Yingkang ,LIN Ke.Effect of RGD Peptides on Endothelial Cell Adhesion and Proliferation on Polyethylene Terephthalate Surfaces[J].Beijing Biomedical Engineering,2003,22(4):278-280.
Authors:WU Zhong  SHI Yingkang  LIN Ke
Institution:WU Zhong 1,SHI Yingkang 2,LIN Ke. 1 Department of Thoracic and Cardiovascular Surgery,Drum Tower Hospital Affiliated to Medical College of Nanjing University,Nanjing 210008,2 Department of Thoracic and Cardiovascular Surgery,West China Hospital of Sichuan University,Chengdu 610041.
Abstract:Many kinds of adhesive proteins contain Arg Gly Asp (RGD) sequence, which is closely related to cell adhesion and proliferation on biomaterial surfaces. In this study,cultured human umbilical vein endothelial cells (HUVEC) were seeded on polyethylene terephthalate (PET) surfaces, which were precoated with fibronectin, or covalently grafted with synthetic bioactive RGD peptides respectively. The results showed that synthetic RGD peptides could remarkably improve cell attachment and proliferation on PET surfaces. Compared with fibronectin, RGD showed more significant cell adhesion activity, while there was no obvious difference of proliferation activity between fibronectin and RGD peptide. This study provides a feasible idea of biomaterial surface modification, and may improve clinical results of endothelialized biomaterials.
Keywords:Arg  Gly  Asp(RGD)    Polyethylene terephthalate (PET)    Endothelial cell    Adhesion    Proliferation
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