RGD-peptides for tissue engineering of articular cartilage

被引:120
作者
Jeschke, B [1 ]
Meyer, J
Jonczyk, A
Kessler, H
Adamietz, P
Meenen, NM
Kantlehner, M
Goepfert, C
Nies, B
机构
[1] Merck Biomat GmbH, R&D, D-64271 Darmstadt, Germany
[2] Merck KGaA, Preclin Res, D-64271 Darmstadt, Germany
[3] Tech Univ Munich, Inst Organ Chem & Biochem, D-85747 Garching, Germany
[4] Univ Krankenhaus Eppendorf, IMBM, D-20246 Hamburg, Germany
[5] Univ Krankenhaus Eppendorf, Chirurg Klin & Poliklin, D-20246 Hamburg, Germany
关键词
surface modification; RGD-peptide; FACS; adhesion; chondrocyte; cartilage;
D O I
10.1016/S0142-9612(02)00052-2
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
One keypoint in the development of a biohybrid implant for articular cartilage defects is the specific binding of cartilage cells to a supporting structure. Mimicking the physiological adhesion process of chondrocytes to the extracellular matrix is expected to improve cell adhesion of in Vitro cultured chondrocytes. Our approach involves coating of synthetic scaffolds with tailor-made, cyclic RGD-peptides, which bind to specific integrin receptors on the cell surface. In this Study we investigated the expression pattern of integrins on the cell surface of chondrocytes and their capability to specifically bind to RGD-peptide coated materials in the Course of monolayer cultivation. Human chondrocytes expressed integrins during a cultivation period of 20 weeks. Receptors proved to be functionally active Lis human and pig chondrocytes attached to RGD-coated surfaces. A competition assay with soluble RGD-peptide revealed binding specificity to the RGD-entity. Chondrocyte morpholoy changed with increasing amounts of cyclic RGD-peptides on the surface. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3455 / 3463
页数:9
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