Effect of multiple unconfined compression on cellular dense collagen scaffolds for bone tissue engineering

被引:67
作者
Bitar, Malak
Salih, Vehid
Brown, Robert A.
Nazhat, Showan N.
机构
[1] UCL, Eastman Dent Inst, Div Biomat & Tissue Engn, London WC1X 8LD, England
[2] UCL, Tissue Repair & Engn, Stanmore HA7 4LP, Middx, England
[3] McGill Univ, Dept Min Met & Mat Engn, Montreal, PQ H3A 2B2, Canada
关键词
D O I
10.1007/s10856-006-0685-1
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Plastic compression of hydrated collagen gels rapidly produces biomimetic scaffolds of improved mechanical properties. These scaffolds can potentially be utilised as cell seeded systems for bone tissue engineering. This work investigated the influence of multiple unconfined compression on the biocompatibility and mechanical properties of such systems. Single and double compressed dense collagen matrices were produced and characterised for protein dry weight, morphology and mechanical strength. Compression related maintenance of the seeded HOS TE85 cell line viability in relation to the extent of compression was evaluated up to 10 days in culture using the TUNEL assay. Fluorescence Live/Dead assay was conducted to examine overall cell survival and morphology. Cell induced structural changes in the dense collagenous scaffolds were assessed by routine histology. The mechanical properties of the cellular scaffolds were also evaluated as a function of time in culture. It is clear that a single plastic compression step produced dense collagenous scaffolds capable of maintaining considerable cell viability and function as signs of matrix remodeling, and maintenance of mechanical properties were evident. Such scaffolds should therefore be further developed as systems for bone tissue regeneration.
引用
收藏
页码:237 / 244
页数:8
相关论文
共 29 条
  • [1] Use of multiple unconfined compression for control of collagen gel scaffold density and mechanical properties
    Abou Neel, Ensanya A.
    Cheema, Umber
    Knowles, Jonathan C.
    Brown, Robert A.
    Nazhat, Showan N.
    [J]. SOFT MATTER, 2006, 2 (11) : 986 - 992
  • [2] INSITU END-LABELING DETECTS DNA STRAND BREAKS IN APOPTOSIS AND OTHER PHYSIOLOGICAL AND PATHOLOGICAL STATES
    ANSARI, B
    COATES, PJ
    GREENSTEIN, BD
    HALL, PA
    [J]. JOURNAL OF PATHOLOGY, 1993, 170 (01) : 1 - 8
  • [3] PRODUCTION OF A TISSUE-LIKE STRUCTURE BY CONTRACTION OF COLLAGEN LATTICES BY HUMAN-FIBROBLASTS OF DIFFERENT PROLIFERATIVE POTENTIAL INVITRO
    BELL, E
    IVARSSON, B
    MERRILL, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (03) : 1274 - 1278
  • [4] CLEAVAGE OF DNA TO LARGE KILOBASE PAIR FRAGMENTS OCCURS IN SOME FORMS OF NECROSIS AS WELL AS APOPTOSIS
    BICKNELL, GR
    COHEN, GM
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 207 (01) : 40 - 47
  • [5] Born again bone: Tissue engineering for bone repair
    Braddock, M
    Houston, P
    Campbell, C
    Ashcroft, P
    [J]. NEWS IN PHYSIOLOGICAL SCIENCES, 2001, 16 : 208 - 213
  • [6] Ultrarapid engineering of biomimetic materials and tissues: Fabrication of nano- and microstructures by plastic compression
    Brown, RA
    Wiseman, M
    Chuo, CB
    Cheema, U
    Nazhat, SN
    [J]. ADVANCED FUNCTIONAL MATERIALS, 2005, 15 (11) : 1762 - 1770
  • [7] Tissue engineering and cell therapy of cartilage and bone
    Cancedda, R
    Dozin, B
    Giannoni, P
    Quarto, R
    [J]. MATRIX BIOLOGY, 2003, 22 (01) : 81 - 91
  • [8] A cautionary note on the use of the TUNEL stain to determine apoptosis
    CharriautMarlangue, C
    BenAri, Y
    [J]. NEUROREPORT, 1995, 7 (01) : 61 - 64
  • [9] Identification of necrotic cell death by the TUNEL assay in the hypoxic-ischemic neonatal rat brain
    deTorres, C
    Munell, F
    Ferrer, I
    Reventos, J
    Macaya, A
    [J]. NEUROSCIENCE LETTERS, 1997, 230 (01) : 1 - 4
  • [10] Nanometer analysis of cell spreading on matrix-coated surfaces reveals two distinct cell states and STEPs
    Dubin-Thaler, BJ
    Giannone, G
    Döbereiner, HG
    Sheetz, MP
    [J]. BIOPHYSICAL JOURNAL, 2004, 86 (03) : 1794 - 1806