Characterization and phenotypic stability of human disc cells in vitro

被引:77
作者
Gruber, HE
Stasky, AA
Hanley, EN
机构
[1] Department of Orthopedic Surgery, Carolinas Medical Center, Charlotte, NC
关键词
collagen; disc; extracellular matrix; human annulus; proteoglycans; tissue culture;
D O I
10.1016/S0945-053X(97)90016-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Successful in vitro studies of disc cells require interaction of the cell with a compatible microenvironment which favors expression of the disc cell phenotype. The objective of this study was to characterize cells grown by standardized methods of isolation and passage, and culture cells from the human annulus in three-dimensional culture. Cells from the annulus of 11 individuals were cultured in alginate or agarose for ten days, and extracellular matrix components were evaluated with immunohistochemistry and quantitative analysis of the percent of colonies producing Type I or II collagen, 4-sulfated chondroitin sulfate or keratan sulfate. Results show production of these four extracellular matrix products through multiple passages and support the phenotypic stability of disc cells in three-dimensional culture.
引用
收藏
页码:285 / 288
页数:4
相关论文
共 8 条
  • [1] The human lumbar intervertebral disc - Evidence for changes in the biosynthesis and denaturation of the extracellular matrix with growth, maturation, ageing, and degeneration
    Antoniou, J
    Steffen, T
    Nelson, F
    Winterbottom, N
    Hollander, AP
    Poole, RA
    Aebi, M
    Alini, M
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (04) : 996 - 1003
  • [2] DIFFERENCES BETWEEN SUB-POPULATIONS OF CULTURED BOVINE ARTICULAR CHONDROCYTES .1. MORPHOLOGY AND CARTILAGE MATRIX PRODUCTION
    AYDELOTTE, MB
    KUETTNER, KE
    [J]. CONNECTIVE TISSUE RESEARCH, 1988, 18 (03) : 205 - 222
  • [3] DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS
    BENYA, PD
    SHAFFER, JD
    [J]. CELL, 1982, 30 (01) : 215 - 224
  • [4] CHELBERG MK, 1995, J ANAT, V186, P43
  • [5] HANLEY ENJ, 1992, DIAGNOSIS TREATMENT, P125
  • [6] HAUSELMANN HJ, 1994, J CELL SCI, V107, P17
  • [7] KOLETTAS E, 1995, J CELL SCI, V108, P1991
  • [8] SCHWOB JE, 1992, J NEUROSCI, V12, P3896