Major biological obstacles for persistent cell-based regeneration of articular cartilage

被引:248
作者
Steinert, Andre F. [1 ]
Ghivizzani, Steven C.
Rethwilm, Axel
Tuan, Rocky S.
Evans, Christopher H.
Noeth, Ulrich
机构
[1] Univ Wurzburg, Orthopaed Ctr Musculoskeletal Res, Konig Ludwig Haus, Wurzburg, Germany
[2] Univ Florida, Dept Orthopaed & Rehabil, Gainesville, FL USA
[3] Univ Wurzburg, Inst Virol & Immunbiol, D-8700 Wurzburg, Germany
[4] NIAMSD, Cartilage Biol & Orthopaed Branch, Dept Hlth & Human Serv, NIH, Bethesda, MD USA
[5] Harvard Univ, Sch Med, Ctr Mol Orthopaed, Boston, MA USA
关键词
D O I
10.1186/ar2195
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hyaline articular cartilage, the load-bearing tissue of the joint, has very limited repair and regeneration capacities. The lack of efficient treatment modalities for large chondral defects has motivated attempts to engineer cartilage constructs in vitro by combining cells, scaffold materials and environmental factors, including growth factors, signaling molecules, and physical influences. Despite promising experimental approaches, however, none of the current cartilage repair strategies has generated long lasting hyaline cartilage replacement tissue that meets the functional demands placed upon this tissue in vivo. The reasons for this are diverse and can ultimately result in matrix degradation, differentiation or integration insufficiencies, or loss of the transplanted cells and tissues. This article aims to systematically review the different causes that lead to these impairments, including the lack of appropriate differentiation factors, hypertrophy, senescence, apoptosis, necrosis, inflammation, and mechanical stress. The current conceptual basis of the major biological obstacles for persistent cell-based regeneration of articular cartilage is discussed, as well as future trends to overcome these limitations.
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页数:15
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共 212 条
[61]   Direct adenovirus-mediated gene transfer of interleukin 1 and tumor necrosis factor α soluble receptors to rabbit knees with experimental arthritis has local and distal anti-arthritic effects [J].
Ghivizzani, SC ;
Lechman, ER ;
Kang, R ;
Tio, C ;
Kolls, J ;
Evans, CH ;
Robbins, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (08) :4613-4618
[62]   Autologous chondrocyte implantation (ACI) for aged patients:: development of the proper cell expansion conditions for possible therapeutic applications [J].
Giannoni, P ;
Pagano, A ;
Maggi, E ;
Arbicò, R ;
Randazzo, N ;
Grandizio, M ;
Cancedda, R ;
Dozin, B .
OSTEOARTHRITIS AND CARTILAGE, 2005, 13 (07) :589-600
[63]   Articular chondrocyte culturing for cell-based cartilage repair: Needs and perspectives [J].
Giannoni, Paolo ;
Cancedda, Ranieri .
CELLS TISSUES ORGANS, 2006, 184 (01) :1-15
[64]   Apoptotic chondrocyte death in cell-matrix biocomposites used in autologous chondrocyte transplantation [J].
Gille, J ;
Ehlers, EM ;
Okroi, M ;
Russlies, M ;
Behrens, P .
ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER, 2002, 184 (04) :325-332
[65]   The control of chondrogenesis [J].
Goldring, MB ;
Tsuchimochi, K ;
Ijiri, K .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2006, 97 (01) :33-44
[66]   Lentiviral-mediated gene delivery to synovium: Potent intra-articular expression with amplification by inflammation [J].
Gouze, E ;
Pawliuk, R ;
Gouze, JN ;
Pilapil, C ;
Fleet, C ;
Palmer, GD ;
Evans, CH ;
Leboulch, P ;
Ghivizzani, SC .
MOLECULAR THERAPY, 2003, 7 (04) :460-466
[67]   In vivo gene delivery to synovium by lentiviral vectors [J].
Gouze, E ;
Pawliuk, R ;
Pilapil, C ;
Gouze, JN ;
Fleet, C ;
Palmer, GD ;
Evans, CH ;
Leboulch, P ;
Ghivizzani, SC .
MOLECULAR THERAPY, 2002, 5 (04) :397-404
[68]   A comparative study of the inhibitory effects of interleukin-1 receptor antagonist following administration as a recombinant protein or by gene transfer [J].
Gouze, JN ;
Gouze, E ;
Palmer, GD ;
Liew, VS ;
Pascher, A ;
Betz, OB ;
Thornhill, TS ;
Evans, CH ;
Grodzinsky, AJ ;
Ghivizzani, SC .
ARTHRITIS RESEARCH & THERAPY, 2003, 5 (05) :R301-R309
[69]   Stem cells as platforms for delivery of genes to enhance cartilage repair [J].
Grande, DA ;
Mason, J ;
Light, E ;
Dines, D .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A :111-116
[70]   Biomechanical assessment of tissue retrieved after in vivo cartilage defect repair: tensile modulus of repair tissue and integration with host cartilage [J].
Gratz, KR ;
Wong, VW ;
Chen, AC ;
Fortier, LA ;
Nixon, AJ ;
Sah, RL .
JOURNAL OF BIOMECHANICS, 2006, 39 (01) :138-146