The Effect of Continuous Culture on the Growth and Structure of Tissue-Engineered Cartilage

被引:27
作者
Khan, Aasma A. [1 ,3 ]
Suits, Jocelyne M. T. [1 ,3 ]
Kandel, Rita A. [4 ]
Waldman, Stephen D. [1 ,2 ,3 ]
机构
[1] Queens Univ, Dept Chem Engn, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Dept Mech & Mat Engn, Kingston, ON K7L 3N6, Canada
[3] Kingston Gen Hosp, Human Mobil Res Ctr, Kingston, ON K7L 2V7, Canada
[4] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
chondrocytes; exracellular matrix; cartilage; tissue engineering; bioreactors; glucose metabolism; continuous culture; ARTICULAR-CARTILAGE; BIOREACTOR CULTIVATION; GLUCOSE-CONCENTRATION; CHONDROCYTES; PERFUSION; COLLAGEN; METABOLISM; GLYCOSAMINOGLYCAN; VIABILITY; EXPLANTS;
D O I
10.1002/btpr.108
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The use of bioreactors for cartilage tissue engineering has become increasingly important as traditional batch-fed culture is not optimal for in vitro tissue growth. Most tissue engineering bioreactors rely on convection as the primary means to provide mass transfer; however, convective transport can also impart potentially unwanted and/or uncontrollable mechanical stimuli to the cells resident in the construct. The reliance on diffusive transport may not necessarily be ineffectual as previous studies have observed improved cartilaginous tissue growth when the constructs were cultured in elevated volumes of media. In this study, to approximate an infinite reservoir of media, we investigated the effect of continuous culture on cartilaginous tissue growth in vitro. Isolated bovine articular chondrocytes were seeded in high density, 3D culture on Millicell (TM) filters. After two weeks of preculture, the constructs were cultivated with or without continuous media flow (5-10 mu L/min) for a period of one week. Tissue engineered cartilage constructs grown under continuous media flow significantly accumulated more collagen and proteoglycans (increased by 50-70%). These changes were similar in magnitude to the reported effect of through-thickness perfusion without the need for large volumetric flow rates (5-10 mu L/min as opposed to 240-800 mu L/min). Additionally, tissues grown in the reactor displayed some evidence of the stratified morphology of native cartilage as well as containing stores of intracellular glycogen. Future studies will investigate the effect of long-term continuous culture in terms of extracellular matrix accumulation and subsequent changes in mechanical function. (C) 2009 American Institute of Chemical Engineers Biotechnol. Prog., 25: 508-515, 2009
引用
收藏
页码:508 / 515
页数:8
相关论文
共 58 条
[1]   A COLORIMETRIC ASSAY FOR THE MEASUREMENT OF D-GLUCOSE CONSUMPTION BY CULTURED-CELLS [J].
BLAKE, DA ;
MCLEAN, NV .
ANALYTICAL BIOCHEMISTRY, 1989, 177 (01) :156-160
[2]   CHARACTERIZATION OF PROTEOGLYCAN ACCUMULATION DURING FORMATION OF CARTILAGENOUS TISSUE IN-VITRO [J].
BOYLE, J ;
LUAN, B ;
CRUZ, TF ;
KANDEL, RA .
OSTEOARTHRITIS AND CARTILAGE, 1995, 3 (02) :117-125
[3]  
Brandt KD., 1998, Composition and structure of articular cartilage. Osteoarthritis, P110
[4]   ENGINEERING OF CARTILAGE TISSUE USING BIORESORBABLE POLYMER FLEECES AND PERFUSION CULTURE [J].
BUJIA, J ;
SITTINGER, M ;
MINUTH, WW ;
HAMMER, C ;
BURMESTER, G ;
KASTENBAUER, E .
ACTA OTO-LARYNGOLOGICA, 1995, 115 (02) :307-310
[5]   CHONDROCYTES IN AGAROSE CULTURE SYNTHESIZE A MECHANICALLY FUNCTIONAL EXTRACELLULAR-MATRIX [J].
BUSCHMANN, MD ;
GLUZBAND, YA ;
GRODZINSKY, AJ ;
KIMURA, JH ;
HUNZIKER, EB .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1992, 10 (06) :745-758
[6]  
Chevrier A, 2005, J HISTOTECHNOL, V28, P165
[7]   Perfusion increases cell content and matrix synthesis in chondrocyte three-dimensional cultures [J].
Davisson, T ;
Sah, RL ;
Ratcliffe, A .
TISSUE ENGINEERING, 2002, 8 (05) :807-816
[8]   IMPROVED QUANTITATION AND DISCRIMINATION OF SULFATED GLYCOSAMINOGLYCANS BY USE OF DIMETHYLMETHYLENE BLUE [J].
FARNDALE, RW ;
BUTTLE, DJ ;
BARRETT, AJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 883 (02) :173-177
[9]   Tissue engineering of cartilage in space [J].
Freed, LE ;
Langer, R ;
Martin, I ;
Pellis, NR ;
VunjakNovakovic, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (25) :13885-13890
[10]   AN IMPROVED METHOD FOR DETERMINING PROTEOGLYCANS SYNTHESIZED BY CHONDROCYTES IN CULTURE [J].
GOLDBERG, RL ;
KOLIBAS, LM .
CONNECTIVE TISSUE RESEARCH, 1990, 24 (3-4) :265-275