Osteoarthritis-derived chondrocytes are a potential source of multipotent progenitor cells for cartilage tissue engineering

被引:15
作者
Oda, Tomoyuki [1 ]
Sakai, Tadahiro [1 ]
Hiraiwa, Hideki [1 ]
Hamada, Takashi [1 ]
Ono, Yohei [1 ]
Nakashima, Motoshige [1 ]
Ishizuka, Shinya [1 ]
Matsukawa, Tetsuya [1 ]
Yamashita, Satoshi [1 ]
Tsuchiya, Saho [1 ]
Ishiguro, Naoki [1 ]
机构
[1] Nagoya Univ, Dept Orthopaed Surg, Sch Med, Showa Ku, 65 Tsurumai Cho, Nagoya, Aichi 4668550, Japan
基金
日本学术振兴会;
关键词
Autologous chondrocyte implantation; Cartilage tissue engineering; Chondrocytes; Multipotency; Osteoarthritis; HUMAN ARTICULAR CHONDROCYTES; MESENCHYMAL STEM-CELLS; BONE-MARROW; IN-VITRO; CHONDROGENIC DIFFERENTIATION; SURFACE-MARKERS; CULTURE; MATRIX; TRANSPLANTATION; EXPRESSION;
D O I
10.1016/j.bbrc.2016.09.085
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
The natural healing capacity of damaged articular cartilage is poor, rendering joint surface injuries a prime target for regenerative medicine. While autologous chondrocyte or mesenchymal stem cell (MSC) implantation can be applied to repair cartilage defects in young patients, no appropriate long-lasting treatment alternative is available for elderly patients with osteoarthritis (OA). Multipotent progenitor cells are reported to present in adult human articular cartilage, with a preponderance in OA cartilage. These facts led us to hypothesize the possible use of osteoarthritis-derived chondrocytes as a cell source for cartilage tissue engineering. We therefore analyzed chondrocyte- and stem cell-related markers, cell growth rate, and multipotency in OA chondrocytes (OACs) and bone marrow-derived MSCs, along with normal articular chondrocytes (ACS) as a control. OACs demonstrated similar phenotype and proliferation rate to MSCs. Furthermore, OACs exhibited multilineage differentiation ability with a greater chondrogenic differentiation ability than MSCs, which was equivalent to ACs. We conclude that chondrogenic capacity is not significantly affected by OA, and OACs could be a potential source of multipotent progenitor cells for cartilage tissue engineering. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:469 / 475
页数:7
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