A biomimetic extracellular matrix for cartilage tissue engineering centered on photocurable gelatin, hyaluronic acid and chondroitin sulfate

被引:357
作者
Levett, Peter A. [1 ,2 ]
Melchels, Ferry P. W. [1 ,2 ]
Schrobback, Karsten [1 ]
Hutmacher, Dietmar W. [1 ]
Malda, Jos [1 ,2 ]
Klein, Travis J. [1 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Kelvin Grove, Qld 4059, Australia
[2] Univ Med Ctr Utrecht, Dept Orthopaed, NL-3508 GA Utrecht, Netherlands
基金
澳大利亚研究理事会;
关键词
Cartilage tissue engineering; Hydrogels; Photopolymerization; Gelatin; Hyaluronic acid; AUTOLOGOUS CHONDROCYTE IMPLANTATION; MESENCHYMAL STEM-CELLS; ARTICULAR-CARTILAGE; PEG HYDROGELS; CHONDROGENIC DIFFERENTIATION; ZONAL CHONDROCYTES; COLLAGEN; REPAIR; EXPRESSION; MMP-13;
D O I
10.1016/j.actbio.2013.10.005
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The development of hydrogels tailored for cartilage tissue engineering has been a research and clinical goal for over a decade. Directing cells towards a chondrogenic phenotype and promoting new matrix formation are significant challenges that must be overcome for the successful application of hydrogels in cartilage tissue therapies. Gelatin-methacrylamide (Gel-MA) hydrogels have shown promise for the repair of some tissues, but have not been extensively investigated for cartilage tissue engineering. We encapsulated human chondrocytes in Gel-MA-based hydrogels, and show that with the incorporation of small quantities of photocrosslinkable hyaluronic acid methacrylate (HA-MA), and to a lesser extent chondroitin sulfate methacrylate (CS-MA), chondrogenesis and mechanical properties can be enhanced. The addition of HA-MA to Gel-MA constructs resulted in more rounded cell morphologies, enhanced chondrogenesis as assessed by gene expression and immunofluorescence, and increased quantity and distribution of the newly synthesized extracellular matrix (ECM) throughout the construct. Consequently, while the compressive moduli of control Gel-MA constructs increased by 26 kPa after 8 weeks culture, constructs with HA-MA and CS-MA increased by 114 kPa. The enhanced chondrogenic differentiation, distribution of ECM, and improved mechanical properties make these materials potential candidates for cartilage tissue engineering applications. (C) 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:214 / 223
页数:10
相关论文
共 55 条
[1]
Akmal M, 2005, J BONE JOINT SURG BR, V87B, P1143, DOI 10.1302/0301-620X.87B8
[2]
Gene expression and cell differentiation in matrix-associated chondrocyte transplantation grafts: a comparative study [J].
Albrecht, C. ;
Tichy, B. ;
Nuernberger, S. ;
Hosiner, S. ;
Zak, L. ;
Aldrian, S. ;
Marlovits, S. .
OSTEOARTHRITIS AND CARTILAGE, 2011, 19 (10) :1219-1227
[3]
Allemann M, 2001, J BIOMED MATER RES, V55, P13
[4]
Benton JA, 2009, TISSUE ENG PT A, V15, P3221, DOI [10.1089/ten.tea.2008.0545, 10.1089/ten.TEA.2008.0545]
[5]
DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[6]
Billinghurst RC, 1997, J CLIN INVEST, P99
[7]
TREATMENT OF DEEP CARTILAGE DEFECTS IN THE KNEE WITH AUTOLOGOUS CHONDROCYTE TRANSPLANTATION [J].
BRITTBERG, M ;
LINDAHL, A ;
NILSSON, A ;
OHLSSON, C ;
ISAKSSON, O ;
PETERSON, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) :889-895
[8]
Cell Carriers as the Next Generation of Cell Therapy for Cartilage Repair A Review of the Matrix-Induced Autologous Chondrocyte Implantation Procedure [J].
Brittberg, Mats .
AMERICAN JOURNAL OF SPORTS MEDICINE, 2010, 38 (06) :1259-1271
[9]
Chondrocyte phenotypes on different extracellular matrix monolayers [J].
Brodkin, KR ;
García, AJ ;
Levenston, ME .
BIOMATERIALS, 2004, 25 (28) :5929-5938
[10]
Synthesis and characterization of photopolymerized multifunctional hydrogels: Water-soluble poly(vinyl alcohol) and chondroitin sulfate macromers for chondrocyte encapsulation [J].
Bryant, SJ ;
Davis-Arehart, KA ;
Luo, N ;
Shoemaker, RK ;
Arthur, JA ;
Anseth, KS .
MACROMOLECULES, 2004, 37 (18) :6726-6733