Hersel Ulrich, Dahmen Claudia, Kessler Horst
Institut für Organische Chemie und Biochemie, Technische Universität München, Lichtenbergstr. 4, D-85747, Garching, Germany.
Biomaterials. 2003 Nov;24(24):4385-415. doi: 10.1016/s0142-9612(03)00343-0.
Since RGD peptides (R: arginine; G: glycine; D: aspartic acid) have been found to promote cell adhesion in 1984 (Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule, Nature 309 (1984) 30), numerous materials have been RGD functionalized for academic studies or medical applications. This review gives an overview of RGD modified polymers, that have been used for cell adhesion, and provides information about technical aspects of RGD immobilization on polymers. The impacts of RGD peptide surface density, spatial arrangement as well as integrin affinity and selectivity on cell responses like adhesion and migration are discussed.
自1984年发现RGD肽(R:精氨酸;G:甘氨酸;D:天冬氨酸)可促进细胞黏附以来(纤连蛋白的细胞附着活性可由该分子的小合成片段复制,《自然》309卷(1984年)第30页),许多材料已被进行RGD功能化处理,用于学术研究或医学应用。本综述概述了已用于细胞黏附的RGD修饰聚合物,并提供了RGD固定在聚合物上的技术方面的信息。讨论了RGD肽表面密度、空间排列以及整合素亲和力和选择性对细胞黏附、迁移等细胞反应的影响。