Effect of insoluble extracellular matrix molecules on Fas expression in epithelial cells

被引:1
作者
Fine, A [1 ]
Miranda, K
Farmer, SR
Anderson, NL
机构
[1] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Boston Vet Adm Hosp, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
关键词
D O I
10.1002/(SICI)1097-4652(199803)174:3<285::AID-JCP2>3.0.CO;2-K
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fas, which functions to initiate a signal causing apoptosis, is expressed in epithelia, thus, suggesting a role in controlling cell number during states of cell and matrix turnover. In view of this, we hypothesized that cell-matrix interactions may be an important determinant of Fas expression in epithelial cells. To investigate this, we examined the effect of insoluble extracellular matrix molecules on Fas expression in murine lung epithelial (MLE) cells, a transformed mouse lung epithelial cell line. We report that ?) insoluble extracellular matrices increased Fas mRNA in a time and concentration-dependent manner; 2) induced increases in Fas mRNA were associated with concomitantly increased Fas protein; and 3) nonspecific adherence to a polylysine substrate did not induce Fas mRNA. Consistent with these findings, Fas-induced apoptosis was significantly enhanced in cultures plated on type IV collagen. Employing rat hepatocytes, we confirmed that the insoluble extracellular matrix also increases Fas expression in primary epithelial cells. By amplifying Fas-mediated apoptosis, these data suggest a mechanism whereby the extracellular matrix regulates the fate of specific epithelial cell populations. (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:285 / 292
页数:8
相关论文
共 40 条
  • [1] TARGETED MUTATION IN THE FAS GENE CAUSES HYPERPLASIA IN PERIPHERAL LYMPHOID ORGANS AND LIVER
    ADACHI, M
    SUEMATSU, S
    KONDO, T
    OGASAWARA, J
    TANAKA, T
    YOSHIDA, N
    NAGATA, S
    [J]. NATURE GENETICS, 1995, 11 (03) : 294 - 300
  • [2] BARTON WM, 1995, AM J RESP CRIT CARE, V151, pA164
  • [3] STRUCTURE OF THE HUMAN APO-1 GENE
    BEHRMANN, I
    WALCZAK, H
    KRAMMER, PH
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (12) : 3057 - 3062
  • [4] SUPPRESSION OF ICE AND APOPTOSIS IN MAMMARY EPITHELIAL-CELLS BY EXTRACELLULAR-MATRIX
    BOUDREAU, N
    SYMPSON, CJ
    WERB, Z
    BISSELL, MJ
    [J]. SCIENCE, 1995, 267 (5199) : 891 - 893
  • [5] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [6] CLARK RAF, 1990, INVEST DERMATOL, V6, pS128
  • [7] COLUMBANO A, 1985, LAB INVEST, V52, P670
  • [8] JAK-STAT PATHWAYS AND TRANSCRIPTIONAL ACTIVATION IN RESPONSE TO IFNS AND OTHER EXTRACELLULAR SIGNALING PROTEINS
    DARNELL, JE
    KERR, IM
    STARK, GR
    [J]. SCIENCE, 1994, 264 (5164) : 1415 - 1421
  • [9] DESPREZ PY, 1995, MOL CELL BIOL, V15, P3398
  • [10] DHAWAN J, 1991, J BIOL CHEM, V266, P8470