Combining chondrocytes and smooth muscle cells to engineer hybrid soft tissue constructs

被引:63
作者
Brown, AN
Kim, BS
Alsberg, E
Mooney, DJ [1 ]
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biol & Mat Sci, Ann Arbor, MI 48109 USA
来源
TISSUE ENGINEERING | 2000年 / 6卷 / 04期
关键词
D O I
10.1089/107632700418029
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Engineering new tissues using cell transplantation may provide a valuable tool for reconstructive surgery applications. Chondrocyte transplantation in particular has been successfully used to engineer new tissue masses due to the low metabolic requirements of these cells. However, the engineered cartilaginous tissue is too rigid for many soft tissue applications. We propose that hybrid tissue engineered from chondrocytes and smooth muscle cells could reflect mechanical properties intermediate between these two cell types. In this study, rat aortic smooth muscle cells and pig auricular chondrocytes were co-cultured on polyglycolic acid fiber-based matrices to address this hypothesis. Mixed cell suspensions were seeded by agitating the polymer matrices and a cell suspension with an orbital shaker. After seeding, cell-polymer constructs were cultured in stirred bioreactors for 8 weeks. The cell density and extracellular matrix (collagen, elastin, and glycosaminoglycan) content of the engineered tissues were determined biochemically. After 8 weeks in culture, the hybrid tissue had a high cell density (5.8 X 10(8) cells/cm(3)), and elastin (519 mu g/g wet tissue sample), collagen (272 mu g/g wet tissue sample), and glycosaminoglycan (GAG; 10 mu g/g wet tissue sample) content. Mechanical testing indicated the compressive modulus of the hybrid tissues after 8 weeks to be 40.8 +/- 4.1 kPa and the equilibrium compressive modulus to be 8.4 +/- 0.8 kPa. Thus, these hybrid tissues exhibited intermediate stiffness; they were less stiff than native cartilage but stiffer than native smooth muscle tissue. This tissue engineering approach may be useful to engineer tissues for a variety of reconstructive surgery applications.
引用
收藏
页码:297 / 305
页数:9
相关论文
共 30 条
  • [11] HASCALL VC, 1982, METHOD ENZYMOL, V82, P769
  • [12] Kim BS, 1998, J BIOMED MATER RES, V41, P322, DOI 10.1002/(SICI)1097-4636(199808)41:2<322::AID-JBM18>3.0.CO
  • [13] 2-M
  • [14] Kim BS, 1998, BIOTECHNOL BIOENG, V57, P46
  • [15] Development of biocompatible synthetic extracellular matrices for tissue engineering
    Kim, BS
    Mooney, DJ
    [J]. TRENDS IN BIOTECHNOLOGY, 1998, 16 (05) : 224 - 230
  • [16] FLUOROMETRIC ASSAY OF DNA IN CARTILAGE EXPLANTS USING HOECHST-33258
    KIM, YJ
    SAH, RLY
    DOONG, JYH
    GRODZINSKY, AJ
    [J]. ANALYTICAL BIOCHEMISTRY, 1988, 174 (01) : 168 - 176
  • [17] The neointima formed in endothelial cell sodded ePTFE vascular grafts results from both cellular-hyperplasia and extracellular-hypertrophy
    Kleinert, LB
    Hoying, JB
    Williams, SK
    [J]. CELL TRANSPLANTATION, 1996, 5 (04) : 475 - 482
  • [18] TISSUE ENGINEERING
    LANGER, R
    VACANTI, JP
    [J]. SCIENCE, 1993, 260 (5110) : 920 - 926
  • [19] DEVELOPMENT OF BIOMECHANICAL PROPERTIES AND MORPHOGENESIS OF IN-VITRO TISSUE ENGINEERED CARTILAGE
    MA, PX
    SCHLOO, B
    MOONEY, D
    LANGER, R
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (12): : 1587 - 1595
  • [20] ANALYSIS OF COLLAGEN TYPES SYNTHESIZED BY RABBIT EAR CARTILAGE CHONDROCYTES INVIVO AND INVITRO
    MADSEN, K
    VONDERMARK, K
    VANMENXEL, M
    FRIBERG, U
    [J]. BIOCHEMICAL JOURNAL, 1984, 221 (01) : 189 - 196