Aged bovine chondrocytes display a diminished capacity to produce a collagen-rich, mechanically functional cartilage extracellular matrix

被引:83
|
作者
Tran-Khanh, N
Hoemann, CD
McKee, MD
Henderson, JE
Buschmann, MD
机构
[1] Ecole Polytech, Dept Chem & Biomed Engn, Inst Biomed Engn, Montreal, PQ H3C 3A7, Canada
[2] Ecole Polytech, Dept Chem Engn, Montreal, PQ H3C 3A7, Canada
[3] McGill Univ, Fac Dent, Montreal, PQ H3A 2B2, Canada
[4] McGill Univ, Dept Anat & Cell Biol, Montreal, PQ H3A 2B2, Canada
[5] McGill Univ, Fac Med, Ctr Bone & Periodontal Res, Montreal, PQ H3A 1A4, Canada
基金
加拿大健康研究院;
关键词
chondrocyte; ageing; collagen; biomechanics; tissue engineering; cartilage repair;
D O I
10.1016/j.orthres.2005.05.009
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Most fundamental studies in cartilage tissue engineering investigate the ability of chondrocytes from young animals to produce cartilaginous matrix under various conditions, while current clinical applications such as autologous chondrocyte implantation, use chondrocytes from donors that are decades past skeletal maturity. Previous investigations have suggested that several characteristics of primary chondrocytes are age-dependent but none have quantified cell proliferation, proteoglycan synthesis and accumulation, collagen synthesis and accumulation, compressive and tensile mechanical properties in order to examine the effects of donor age on all of these parameters. We enzymatically isolated primary bovine chondrocytes from fetal, young and aged animals and cultured these cells in agarose gels to assess the above-mentioned properties. We found that fetal and young (but still skeletally mature i.e. 18-month-old bovine) chondrocytes behaved similarly, while aged chondrocytes (5- to 7-year-old bovine) displayed diminished proliferation (similar to 2x less), a slightly reduced proteoglycan accumulation per cell (similar to 20%), and significantly less collagen accumulation per cell (similar to 55%) compared to the younger cells. Histological observations and mechanical properties supported these findings, where a particularly significant reduction in tensile stiffness produced by aged chondrocytes compared to younger cells was observed. Our findings suggest that donor age is an important factor in determining the outcome and potential success when tissue-engineered cartilage is produced from articular chondrocytes. More specifically, primary chondrocytes from aged donors may not possess sufficient capacity to produce the extracellular matrix that is required for a mechanically resilient tissue. (c) 2005 Orthopaedic Research Society. Published by Elsevier Ltd. All rights reserved.
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页码:1354 / 1362
页数:9
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