Chitosan-alginate as scaffolding material for cartilage tissue engineering

被引:174
作者
Li, ZS [1 ]
Zhang, MQ [1 ]
机构
[1] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
关键词
tissue engineering; chitosan; alginate; chondrocyte; scaffold;
D O I
10.1002/jbm.a.30449
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Tissue compatibility of chitosan-alginate scaffolds was studied in vitro in terms of cell morphology, proliferation, and functionality using HTB-94 cells. The scaffold has an interconnected 3D porous structure, and was fabricated by thermally induced phase separation followed by freeze drying. Cell proliferation on the chitosan-alginate scaffold was found to be faster than on a pure chitosan scaffold. After cell culture for 2 weeks in vitro, the cells on the chitosan scaffold gradually assumed a fibroblast-like morphology while the cells on the chitosan-alginate scaffold retained their spherical morphology throughout the period of study. SDS-PAGE electrophoresis and Western blot assays for proteins extracted from cells grown on scaffolds indicated that production of cartilage-specific collagen type II, a marker for chondrocytic phenotype, increased from week 2 to week 3 on the chitosan-alginate scaffold but decreased on the chitosan scaffold. This study suggested that chitosan-alginate scaffolds promote cell proliferation, enhance phenotype expression of HTB-94 chondrocytes, and may potentially serve as an improved alternative to chitosan scaffolds for cartilage tissue engineering. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:485 / 493
页数:9
相关论文
共 49 条
[1]
Aigner J, 1998, J BIOMED MATER RES, V42, P172, DOI 10.1002/(SICI)1097-4636(199811)42:2<172::AID-JBM2>3.0.CO
[2]
2-M
[3]
DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[4]
MODULATION AND REEXPRESSION OF THE CHONDROCYTE PHENOTYPE - MEDIATION BY CELL-SHAPE AND MICROFILAMENT MODIFICATION [J].
BENYA, PD .
PATHOLOGY AND IMMUNOPATHOLOGY RESEARCH, 1988, 7 (1-2) :51-54
[5]
Polymer/alginate amalgam for cartilage-tissue engineering [J].
Caterson, EJ ;
Li, WJ ;
Nesti, LJ ;
Albert, T ;
Danielson, K ;
Tuan, RS .
REPARATIVE MEDICINE: GROWING TISSUES AND ORGANS, 2002, 961 :134-138
[6]
Caterson EJ, 2001, J BIOMED MATER RES, V57, P394, DOI 10.1002/1097-4636(20011205)57:3<394::AID-JBM1182>3.0.CO
[7]
2-9
[8]
Optimization of chondrocyte expansion in culture -: Effect of TGFβ-2, bFGF and L-ascorbic acid on bovine articular chondrocytes [J].
de Haart, M ;
Marijnissen, WJCM ;
van Osch, GJVM ;
Verhaar, JAN .
ACTA ORTHOPAEDICA SCANDINAVICA, 1999, 70 (01) :55-61
[9]
NEOCARTILAGE FORMATION INVITRO AND INVIVO USING CELLS CULTURED ON SYNTHETIC BIODEGRADABLE POLYMERS [J].
FREED, LE ;
MARQUIS, JC ;
NOHRIA, A ;
EMMANUAL, J ;
MIKOS, AG ;
LANGER, R .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (01) :11-23
[10]
Engineered cartilage, bone, joints, and menisci - Potential for temporomandibular joint reconstruction [J].
Glowacki, J .
CELLS TISSUES ORGANS, 2001, 169 (03) :302-308