Short collagen fibers provide control of contraction and permeability in fibroblast-seeded collagen gels

被引:31
作者
Gentleman, E [1 ]
Nauman, EA [1 ]
Dee, KC [1 ]
Livesay, GA [1 ]
机构
[1] Tulane Univ, Dept Biomed Engn, New Orleans, LA 70118 USA
来源
TISSUE ENGINEERING | 2004年 / 10卷 / 3-4期
关键词
D O I
10.1089/107632704323061780
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Tissue engineering may allow for the reconstruction of breast, facial, skin, and other soft tissue defects in the human body. Cell-seeded collagen gels are a logical choice for creating soft tissues because they are biodegradable, mimic the natural tissue, and provide a three-dimensional environment for the cells. The main drawback associated with this approach, however, is the subsequent contraction of the gel by the constituent cells, which severely reduces permeability, initiates apoptosis, and precludes control of the resulting shape and size of the construct. In this study, type I collagen gels were seeded with fibroblasts and cast either with or without the addition of short collagen fibers. Gel contraction was monitored and permeability was assessed after 7 and 14 days in culture. The addition of short collagen fibers both significantly limited contraction and increased permeability of fibroblast-seeded collagen gels. The addition of short collagen fibers had no detrimental effect on cell proliferation, and there were a high number of viable fibroblasts in gels with fibers and gels without fibers. Gels containing short collagen fibers demonstrated permeabilities that were 100 to 1000 times greater than controls and also closely maintained their casting dimensions (never less than 96% of original). By limiting contraction and maintaining permeability, the incorporation of short collagen fibers should enable the creation of larger constructs by allowing for greater nutrient diffusion, and permit the creation of more complicated shapes during gel casting.
引用
收藏
页码:421 / 427
页数:7
相关论文
共 43 条
  • [31] OHSAWA S, 1982, CELL BIOL INT REP, V6, P767, DOI 10.1016/0309-1651(82)90169-2
  • [32] Patrick C.W., 1998, FRONTIERS TISSUE ENG, P369
  • [33] Piggott M., 2002, Load bearing fibre composites, V2nd
  • [34] CHEMOTACTIC ATTRACTION OF HUMAN FIBROBLASTS TO TYPE-I, TYPE-2, AND TYPE-3 COLLAGENS AND COLLAGEN-DERIVED PEPTIDES
    POSTLETHWAITE, AE
    SEYER, JM
    KANG, AH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (02) : 871 - 875
  • [35] ROMPRE P, 1990, IN VITRO CELL DEV B, V26, P983
  • [36] Torres DS, 2000, BIOMATERIALS, V21, P1607
  • [37] Comparative analysis of different collagen-based biomaterials as scaffolds for long-term culture of human fibroblasts
    Vaissiere, G
    Chevallay, B
    Herbage, D
    Damour, O
    [J]. MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING, 2000, 38 (02) : 205 - 210
  • [38] PERIPHERAL ANCHORAGE OF DERMAL EQUIVALENTS
    VALLE, CAL
    AUGER, FA
    ROMPRE, P
    BOUVARD, V
    GERMAIN, L
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 1992, 127 (04) : 365 - 371
  • [39] Wang H L, 2000, Compend Contin Educ Dent, V21, P399
  • [40] WASSERMAN AJ, 1989, SCANNING MICROSCOPY, V3, P1183