The effects of glycosaminoglycan content on the compressive modulus of cartilage engineered in type II collagen scaffolds

被引:60
作者
Pfeiffer, E. [1 ,2 ]
Vickers, S. M. [1 ,2 ]
Frank, E. [3 ]
Grodzinsky, A. J. [3 ]
Spector, M. [1 ,2 ,4 ]
机构
[1] VA Boston Healthcare Syst, Tissue Engn, Boston, MA 02130 USA
[2] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Orthopaed Surg, Boston, MA 02115 USA
关键词
Cartilage; Tissue engineering; Mechanical properties; Modulus; Glycosaminoglycan; Scaffold; Collagen;
D O I
10.1016/j.joca.2008.02.014
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: The current study determined the unconfined compressive modulus of tissue-engineered constructs with varying sulfated glycosaminoglycan (GAG) density produced by goat articular chondrocytes in type II collagen scaffolds prepared with a range of cross-link densities and various times in culture, The purpose of this work is to establish a basis for future studies employing constructs of selected maturity (e.g., 25%. 50%. or 75% normal GAG content) for cartilage repair in vivo. Methods: Porous scaffolds (8 mm diameter by 2 mm thick) were fabricated from porcine type II collagen by freeze-drying, followed by dehydrothermal treatment and carbodiimide cross-linking. In a pilot study, passage 3 adult caprine articular chondrocytes isolated from one goat were grown in scaffolds with six cross-link densities for 2, 3, 4, and 6 weeks (n = 3). The goal was to select scaffold cross-link densities and times in culture that would produce constructs with approximately 25%, 50% and 75% the GAG density of native articular cartilage. Based on the results of the pilot study, chondrocytes from three goats were grown in scaffolds with two cross-link densities for three time periods: 3, 5, and 9 weeks (n = 6: one of the cross-link groups was run in quadruplicate). The equilibrium modulus from unconfined compression testing of these samples was correlated with GAG content. Results: There was a notable increase in GAG density with decreasing cross-link density. Histological analysis verified a chondrogenic phenotype and revealed various amounts of GAG and type II collagen-containing cartilage. The correlation between modulus and GAG density had a linear coefficient of determination of 0.60. One group with a mean GAG density of 22 mu g/mm(3), which was 140% the GAG density of normal caprine articular cartilage, averaged a compressive modulus of 31.5 kPa, which was 10% of caprine articular cartilage tested in this study. Conclusions: The GAG density and modulus of tissue-engineered constructs can be controlled by the degree of cross-linking of type II collagen scaffolds and time in culture. (C) 2008 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1237 / 1244
页数:8
相关论文
共 44 条
[1]
POSITION-RELATED CAPACITY FOR DIFFERENTIATION OF LIMB MESENCHYME IN CELL-CULTURE [J].
AHRENS, PB ;
SOLURSH, M ;
REITER, RS ;
SINGLEY, CT .
DEVELOPMENTAL BIOLOGY, 1979, 69 (02) :436-450
[2]
STAGE-RELATED CAPACITY FOR LIMB CHONDROGENESIS IN CELL-CULTURE [J].
AHRENS, PB ;
SOLURSH, M ;
REITER, RS .
DEVELOPMENTAL BIOLOGY, 1977, 60 (01) :69-82
[3]
INDEPENDENT REGULATION OF COLLAGEN TYPES BY CHONDROCYTES DURING THE LOSS OF DIFFERENTIATED FUNCTION IN CULTURE [J].
BENYA, PD ;
PADILLA, SR ;
NIMNI, ME .
CELL, 1978, 15 (04) :1313-1321
[4]
DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[5]
Differential effects of growth factors on tissue-engineered cartilage [J].
Blunk, T ;
Sieminski, AL ;
Gooch, KJ ;
Courter, DL ;
Hollander, AP ;
Nahir, M ;
Langer, R ;
Vunjak-Novakovic, G ;
Freed, JE .
TISSUE ENGINEERING, 2002, 8 (01) :73-84
[6]
Healing of canine articular cartilage defects treated with microfracture, a type-II collagen matrix, or cultured autologous chondrocytes [J].
Breinan, HA ;
Martin, SD ;
Hsu, HP ;
Spector, M .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2000, 18 (05) :781-789
[7]
ALTERATIONS IN CHONDROCYTE CYTOSKELETAL ARCHITECTURE DURING PHENOTYPIC MODULATION BY RETINOIC ACID AND DIHYDROCYTOCHALASIN-B INDUCED REEXPRESSION [J].
BROWN, PD ;
BENYA, PD .
JOURNAL OF CELL BIOLOGY, 1988, 106 (01) :171-179
[8]
Chiyokura Y., 1996, J ORTHOP SCI, V1, P59
[9]
Cross-linking of dermal sheep collagen using a water-soluble carbodiimide [J].
Damink, LHHO ;
Dijkstra, PJ ;
vanLuyn, MJA ;
vanWachem, PB ;
Nieuwenhuis, P ;
Feijen, J .
BIOMATERIALS, 1996, 17 (08) :765-773
[10]
Analysis of N-cadherin function in limb mesenchymal chondrogenesis in vitro [J].
Delise, AM ;
Tuan, RS .
DEVELOPMENTAL DYNAMICS, 2002, 225 (02) :195-204