Engineered cartilage generated by nasal chondrocytes is responsive to physical forces resembling joint loading

被引:90
作者
Candrian, C. [1 ]
Vonwil, D. [1 ]
Barbero, A. [1 ]
Bonacina, E. [1 ,2 ]
Miot, S. [1 ]
Farhadi, J. [1 ]
Wirz, D. [3 ]
Dickinson, S. [4 ]
Hollander, A. [4 ]
Jakob, M. [1 ]
Li, Z. [5 ]
Alini, M. [5 ]
Heberer, M. [1 ]
Martin, I. [1 ]
机构
[1] Univ Basel Hosp, Inst Surg Res, CH-4031 Basel, Switzerland
[2] Politecn Milan, I-20133 Milan, Italy
[3] Univ Basel, Basel, Switzerland
[4] Univ Bristol, Southmead Hosp, Bristol, Avon, England
[5] AO Res Inst, Davos, Switzerland
来源
ARTHRITIS AND RHEUMATISM | 2008年 / 58卷 / 01期
关键词
D O I
10.1002/art.23155
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To determine whether engineered cartilage generated by nasal chondrocytes (ECN) is responsive to different regimens of loading associated with joint kinematics and previously shown to be stimulatory of engineered cartilage generated by articular chondrocytes (ECA). Methods. Human nasal and articular chondrocytes, harvested from 5 individuals, were expanded and cultured for 2 weeks into porous polymeric scaffolds. The resulting ECN and ECA were then maintained under static conditions or exposed to the following loading regimens: regimen 1, single application of cyclic deformation for 30 minutes; regimen 2, intermittent application of cyclic deformation for a total of 10 days, followed by static culture for 2 weeks; regimen 3, application of surface motion for a total of 10 days. Results. Prior to loading, ECN constructs contained significantly higher amounts of glycosaminoglycan (GAG) and type II collagen compared with ECA constructs. ECN responded to regimen 1 by increasing collagen and proteoglycan synthesis, to regimen 2 by increasing the accumulation of GAG and type II collagen as well as the dynamic modulus, and to regimen 3 by increasing the expression of superficial zone protein, at the messenger RNA level and the protein level, as well as the release of hyaluronan. ECA constructs were overall less responsive to all loading regimens, likely due to the lower extracellular matrix content. Conclusion. Human ECN is responsive to physical forces resembling joint loading and can up-regulate molecules typically involved in joint lubrication. These findings should prompt future in vivo studies exploring the possibility of using nasal chondrocytes as a cell source for articular cartilage repair.
引用
收藏
页码:197 / 208
页数:12
相关论文
共 47 条
[31]   Different response of articular chondrocyte subpopulations to surface motion [J].
Li, Z. ;
Yao, S. ;
Alini, M. ;
Grad, S. .
OSTEOARTHRITIS AND CARTILAGE, 2007, 15 (09) :1034-1041
[32]   Stem-cell-driven regeneration of synovial joints [J].
Mao, JJ .
BIOLOGY OF THE CELL, 2005, 97 (05) :289-301
[33]   Cartilage tissue engineering by expanded goat articular chondrocytes [J].
Miot, S ;
de Freitas, PS ;
Wirz, D ;
Daniels, AU ;
Sims, TJ ;
Hollander, AP ;
Mainil-Varlet, P ;
Heberer, M ;
Martin, I .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2006, 24 (05) :1078-1085
[34]   Effects of in vitro preculture on in vivo development of human engineered cartilage in an ectopic model [J].
Moretti, M ;
Wendt, D ;
Dickinson, SC ;
Sims, TJ ;
Hollander, AP ;
Kelly, DJ ;
Prendergast, PJ ;
Heberer, M ;
Martin, I .
TISSUE ENGINEERING, 2005, 11 (9-10) :1421-1428
[35]   Stem cell-based composite tissue constructs for regenerative medicine [J].
Rahaman, MN ;
Mao, JJ .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 91 (03) :261-284
[36]   Age dependence of biochemical and biomechanical properties of tissue-engineered human septal cartilage [J].
Rotter, N ;
Bonassar, LJ ;
Tobias, G ;
Lebl, M ;
Roy, AK ;
Vacanti, CA .
BIOMATERIALS, 2002, 23 (15) :3087-3094
[37]   BIOSYNTHETIC RESPONSE OF CARTILAGE EXPLANTS TO DYNAMIC COMPRESSION [J].
SAH, RLY ;
KIM, YJ ;
DOONG, JYH ;
GRODZINSKY, AJ ;
PLAAS, AHK ;
SANDY, JD .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1989, 7 (05) :619-636
[38]   Repair of large articular osteochondral defects using hybrid scaffolds and bone marrow-derived mesenchymal stem cells in a rabbit model [J].
Shao, Xinxin ;
Goh, James C. H. ;
Hutmacher, Dietmar W. ;
Lee, Eng Hin ;
Ge Zigang .
TISSUE ENGINEERING, 2006, 12 (06) :1539-1551
[39]   The cellular origin of cartilage-like tissue after periosteal transplantation of full-thickness articular cartilage defects - An experimental study using transgenic rats expressing green fluorescent protein [J].
Shinomiya, R ;
Ochi, M ;
Adachi, N ;
Hachisuka, H ;
Natsu, K ;
Yasunaga, Y .
ACTA ORTHOPAEDICA, 2005, 76 (06) :920-926
[40]   Outcomes of septoplasty [J].
Siegel, NS ;
Gliklich, RE ;
Taghizadeh, F ;
Chang, YC .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2000, 122 (02) :228-232