Autologous chondrocyte implantation (ACI) for aged patients:: development of the proper cell expansion conditions for possible therapeutic applications

被引:74
作者
Giannoni, P
Pagano, A
Maggi, E
Arbicò, R
Randazzo, N
Grandizio, M
Cancedda, R
Dozin, B
机构
[1] Natl Inst Canc Res, Lab Regenerat Med, SC Med Rigenerat, I-16132 Genoa, Italy
[2] Biorigen SRL, I-16122 Genoa, Italy
[3] Ospe S Antonio, UO Ortoped, Genoa, Italy
[4] Univ Genoa, Dipartimento Oncol Biol & Genet, I-16132 Genoa, Italy
关键词
cartilage repair; autologous chondrocyte implantation; chondrocyte; tissue engineering;
D O I
10.1016/j.joca.2005.02.015
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
Objective: Proliferation and chondrogenic commitment of cultured articular chondrocytes are impaired when cells derive from aged donors. In those subjects the feasibility of cell-based therapies for articular surface repair is reduced. Moreover, the use of serum as medium supplement elicits non-physiological responses in cultured chondrocytes. This study was therefore undertaken to identify the expansion culture conditions needed to sustain growth and chondrogenic commitment of chondrocytes harvested from aged human subjects. Design: Articular cartilage was obtained from aged (69-75 years) and from young adult subjects (27-35 years). Chondrocytes were isolated and cultured in serum-free (SF) or in serum-supplemented [fetal calf serum (FCS)] conditions. Chondrocytes were expanded in monolayer for five duplications and processed for RNA extraction and reverse transcriptase-polymerase chain reaction (RT-PCR) analysis. The differentiation potential was assessed by micromass pellet cultures before and after expansion in either culture medium, or after a prolonged exposure to serum followed by a period in SF condition. Results: Only SF-cultured chondrocytes reached five duplications within 25-35 days, maintaining the expression of some chondrogenic markers and without altering the levels of active matrix metalloproteinase 3 (MMP-3). Only the pellets derived from SF-expanded cultures positively stained for cartilage matrix deposition. On the contrary, exposure to serum diminished the proliferation capacities, abolished the differentiation potential in the same cells and elicited transcription of the MMP-3 gene. Shifting culture conditions from FCS to SF resumed growth rates but proper extracellular matrix deposition was only partially restored. Conclusions: The SF conditions have proven valuable to prime cell proliferation and to sustain proper commitment in chondrocytes from aged patients. This culturing approach may represent a therapeutic chance extendable to a range of patients normally excluded from clinical protocols based on autologous chondrocyte implantation (ACI). (C) 2005 OsteoArthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
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页码:589 / 600
页数:12
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