Expansion of bovine chondrocytes on microcarriers enhances redifferentiation

被引:109
作者
Malda, J
Van Blitterswijk, CA
Grojec, M
Martens, DE
Tramper, J
Riesle, J
机构
[1] IsoTis NV, Cartilage Tissue Engn Grp, NL-6720 AB Bilthoven, Netherlands
[2] Univ Twente, Inst Biomed Technol, NL-7500 AE Enschede, Netherlands
[3] Univ Wageningen & Res Ctr, Food & Bioproc Engn Grp, Wageningen, Netherlands
来源
TISSUE ENGINEERING | 2003年 / 9卷 / 05期
关键词
D O I
10.1089/107632703322495583
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Functional cartilage implants for orthopedic surgery or in vitro tissue evaluation can be created from expanded chondrocytes and biodegradable scaffolds. Expansion of chondrocytes in two-dimensional culture systems results in their dedifferentiation. The hallmark of this process is the switch of collagen synthesis from type II to type I. The aim of this study was to evaluate the postexpansion chondrogenic potential of microcarrier-expanded bovine articular chondrocytes in pellet cultures. A selection of microcarriers was screened for initial attachment of chondrocytes. On the basis of those results and additional selection criteria related to clinical application, Cytodex-1 microcarriers were selected for further investigation. Comparable doubling times were obtained in T-flask and microcarrier cultures. During propagation on Cytodex-1 microcarriers, cells acquired a spherical-like morphology and the presence of collagen type II was detected. Both observations are indicative of a differentiated chondrocyte. Pellet cultures of microcarrier-expanded cells showed cartilage-like morphology and staining for proteoglycans and collagen type II after 14 days. In contrast, pellets of T-flask-expanded cells had a fibrous appearance and showed abundant staining only for collagen type I. Therefore, culture of chondrocytes on microcarriers may offer useful and cost-effective cell expansion opportunities in the field of cartilage tissue engineering.
引用
收藏
页码:939 / 948
页数:10
相关论文
共 33 条
[1]
Baker TL, 1997, IN VITRO CELL DEV-AN, V33, P358
[2]
DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[3]
Bouchet BY, 2000, J BIOMED MATER RES, V52, P716, DOI 10.1002/1097-4636(20001215)52:4<716::AID-JBM17>3.3.CO
[4]
2-K
[5]
EFFECT OF GROWTH-FACTORS ON CELL-PROLIFERATION BY HUMAN NASAL SEPTAL CHONDROCYTES CULTURED IN MONOLAYER [J].
BUJIA, J ;
SITTINGER, M ;
WILMES, E ;
HAMMER, C .
ACTA OTO-LARYNGOLOGICA, 1994, 114 (05) :539-543
[6]
ARTICULAR-CARTILAGE REPAIR USING ALLOGENEIC PERICHONDROCYTE-SEEDED BIODEGRADABLE POROUS POLYLACTIC ACID (PLA) - A TISSUE-ENGINEERING STUDY [J].
CHU, CR ;
COUTTS, RD ;
YOSHIOKA, M ;
HARWOOD, FL ;
MONOSOV, AZ ;
AMIEL, D .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (09) :1147-1154
[7]
HYDRODYNAMIC EFFECTS ON ANIMAL-CELLS GROWN IN MICROCARRIER CULTURES [J].
CROUGHAN, MS ;
HAMEL, JF ;
WANG, DIC .
BIOTECHNOLOGY AND BIOENGINEERING, 1987, 29 (01) :130-141
[8]
Cellular interactions and signaling in cartilage development [J].
DeLise, AM ;
Fischer, L ;
Tuan, RS .
OSTEOARTHRITIS AND CARTILAGE, 2000, 8 (05) :309-334
[9]
TRANSPLANTATION OF MICROCARRIER-ATTACHED HEPATOCYTES INTO 90-PERCENT PARTIALLY HEPATECTOMIZED RATS [J].
DEMETRIOU, AA ;
REISNER, A ;
SANCHEZ, J ;
LEVENSON, SM ;
MOSCIONI, AD ;
CHOWDHURY, JR .
HEPATOLOGY, 1988, 8 (05) :1006-1009
[10]
Doran PM., 2000, BIOPROCESS ENG PRINC