Dynamic compression of cartilage constructs engineered from expanded human articular chondrocytes

被引:134
作者
Démarteau, O
Wendt, D
Braccini, A
Jakob, M
Schäfer, D
Heberer, M
Martin, I [1 ]
机构
[1] Univ Basel Hosp, Dept Surg, Basel, Switzerland
[2] Univ Basel Hosp, Res Dept, Basel, Switzerland
关键词
chondrogenesis; tissue engineering; porous scaffold; bioreactor; cartilage repairs; biomechanics; mechanobiology; physical stimulation;
D O I
10.1016/j.bbrc.2003.09.099
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent works have shown that mechanical loading can alter the metabolic activity of chondrocytes cultured in 3D scaffolds. In this study we determined whether the stage of development of engineered cartilaginous constructs (expanded adult human articular chondrocytes/Polyactive foams) regulates the effect of dynamic compression on glycosaminoglycan (GAG) metabolism. Construct maturation depended on the culture time (3-14 days) and the donor (4 individuals). When dynamic compression was subsequently applied for 3 days, changes in GAG synthesized, accumulated, and released were significantly positively correlated to the GAG content of the constructs prior to loading, and resulted in stimulation of GAG formation only in the most developed tissues. Conversely, none of these changes were correlated with the expression of collagen type II mRNA, indicating that the response of chondrocytes to dynamic compression does not depend directly upon the stage of cell differentiation, but rather on the extracellular matrix surrounding the cells. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:580 / 588
页数:9
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