Cytokine-rich autologous serum system for cartilaginous tissue engineering

被引:20
作者
Isogai, Noritaka [1 ]
Nakagawa, Yumiko [1 ]
Suzuki, Koji
Yamada, Ryo
Asamura, Shinichi [1 ]
Hayakawa, Sumio [2 ]
Munakata, Hiroshi [2 ]
机构
[1] Kinki Univ, Sch Med, Dept Plast & Reconstruct Surg, Osaka 589, Japan
[2] Kinki Univ, Sch Med, Dept Biochem, Osaka 589, Japan
关键词
cartilage; cytokine; autologous serum;
D O I
10.1097/SAP.0b013e31814b2cb5
中图分类号
R61 [外科手术学];
学科分类号
摘要
Animal serum used for tissue engineering approaches has unacceptable risk for contamination with infectious agents. In this study, a cytokine-rich autologous serum (CRAS) system was developed. Canine auricular chondrocytes were cultured in medium supplemented with either fetal bovine serum (FBS) or autologous canine serum, alone or supplemented with basic fibroblast growth factor (b-FGF). Cell proliferative capacity was higher in the CRAS cultures than in those cultured in FBS, with greater expression of aggrecan and type II collagen in the b-FGF-supplemented CRAS group. The chondrocytes were seeded onto an ear-shaped biodegradable polymer (poly-L-lactide:E-caprolactone, 50:50) and cultured in a Bioflow reactor for 1 week, using the 3 different culture media indicated above, and subsequently implanted into nude mice. The best outcome (cartilage gene expression and morphologic properties) was seen with tissue-engineered constructs precultured in the b-FGF-supplemented CRAS media. These findings indicate a clinically realizable approach for tissue engineering of cartilaginous structures.
引用
收藏
页码:703 / 709
页数:7
相关论文
共 31 条
[1]
Transforming growth factor-beta: The breaking open of a black box [J].
Alevizopoulos, A ;
Mermod, N .
BIOESSAYS, 1997, 19 (07) :581-591
[2]
The effect of fibroblast growth factor and transforming growth factor-β on porcine chondrocytes and tissue-engineered autologous elastic cartilage [J].
Arévalo-Silva, CA ;
Cao, YL ;
Weng, YL ;
Vacanti, M ;
Rodríguez, A ;
Vacanti, CA ;
Eavey, RD .
TISSUE ENGINEERING, 2001, 7 (01) :81-88
[3]
Bottenstein J, 1979, Methods Enzymol, V58, P94
[4]
Transplantation of chondrocytes utilizing a polymer-cell construct to produce tissue-engineered cartilage in the shape of a human ear [J].
Cao, YL ;
Vacanti, JP ;
Paige, KT ;
Upton, J ;
Vacanti, CA .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1997, 100 (02) :297-302
[5]
Effects of growth factors on cell proliferation and matrix synthesis of low-density, primary bovine chondrocytes cultured in collagen I gels [J].
Chaipinyo, K ;
Oakes, BW ;
van Damme, MPI .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (05) :1070-1078
[6]
ABNORMAL BONE-GROWTH AND SELECTIVE TRANSLATIONAL REGULATION IN BASIC FIBROBLAST GROWTH-FACTOR (FGF-2) TRANSGENIC MICE [J].
COFFIN, JD ;
FLORKIEWICZ, RZ ;
NEUMANN, J ;
MORTHOPKINS, T ;
DORN, GW ;
LIGHTFOOT, P ;
GERMAN, R ;
HOWLES, PN ;
KIER, A ;
OTOOLE, BA ;
SASSE, J ;
GONZALEZ, AM ;
BAIRD, A ;
DOETSCHMAN, T .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (12) :1861-1873
[7]
Transforming growth factor-beta [J].
Cox, DA ;
Maurer, T .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1997, 83 (01) :25-30
[8]
BASIC FIBROBLAST GROWTH-FACTOR (FGF) PROMOTES CARTILAGE REPAIR INVIVO [J].
CUEVAS, P ;
BURGOS, J ;
BAIRD, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 156 (02) :611-618
[9]
STRUCTURAL CHARACTERIZATION AND BIOLOGICAL FUNCTIONS OF FIBROBLAST GROWTH-FACTOR [J].
GOSPODAROWICZ, D ;
FERRARA, N ;
SCHWEIGERER, L ;
NEUFELD, G .
ENDOCRINE REVIEWS, 1987, 8 (02) :95-114
[10]
LOCALIZATION OF A FIBROBLAST GROWTH-FACTOR AND ITS EFFECT ALONE AND WITH HYDROCORTISONE ON 3T3 CELL-GROWTH [J].
GOSPODAROWICZ, D .
NATURE, 1974, 249 (5453) :123-127