COMPARISON OF HUMAN TENASCIN EXPRESSION IN NORMAL, SIMIAN-VIRUS-40-TRANSFORMED AND TUMOR-DERIVED CELL-LINES

被引:36
作者
CARNEMOLLA, B [1 ]
BORSI, L [1 ]
BANNIKOV, G [1 ]
TROYANOVSKY, S [1 ]
ZARDI, L [1 ]
机构
[1] IST NAZL RIC CANC, CELL BIOL LAB, VIALE BENEDETTO XV 10, I-16132 GENOA, ITALY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1992年 / 205卷 / 02期
关键词
D O I
10.1111/j.1432-1033.1992.tb16813.x
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
Tenascin is a polymorphic high-molecular-mass extracellular-matrix glycoprotein composed of six similar subunits. Using two-domain-specific anti-tenascin monoclonal antibodies, we have studied the expression and distribution of tenascin in four cultured normal human fibroblasts, two simian-virus-40-(SV40)-transformed and three tumor-derived (melanoma, rhabdomyosarcoma and fibrosarcoma) cell lines. We found that (a) cultured normal human fibroblasts accumulate considerable amounts of tenascin and retain 60-90% in the extracellular matrix, while they release the remainder into the tissue-culture medium; (b) of the two SV40-transformed counterparts we have tested, the AG-280 cell line accumulates no detectable amounts of tenascin and the WI-38-VA cell line accumulates about 10-times less tenascin than its normal counterpart and releases about 90% of it into the culture medium; (c) some tumor-derived cell lines accumulate considerable amounts of tenascin, but in theses cases, more than 90% is released into the culture media; (d) in normal human fibroblasts, two major tenascin isoforms, generated by alternative splicing of the mRNA precursor, are detectable (280 kDa and 190 kDa, respectively) and the lower-molecular-mass tenascin isoform is accumulated preferentially in the extracellular matrix; (e) in SV40-transformed or tumor-derived cell lines, only the higher-molecular-mass isoform is detectable and it is more sialylated than the tenascin produced by the normal human fibroblast cell lines.
引用
收藏
页码:561 / 567
页数:7
相关论文
共 57 条
  • [1] THE DISTRIBUTION OF IMMUNOREACTIVE TENASCIN IN THE EPITHELIAL-MESENCHYMAL JUNCTIONAL AREAS OF BENIGN AND MALIGNANT SQUAMOUS EPITHELIA
    ANBAZHAGAN, R
    SAKAKURA, T
    GUSTERSON, BA
    [J]. VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1990, 59 (01) : 59 - 63
  • [2] ARBOGAST BW, 1977, J BIOL CHEM, V252, P8863
  • [3] TENASCIN DURING GUT DEVELOPMENT - APPEARANCE IN THE MESENCHYME, SHIFT IN MOLECULAR-FORMS, AND DEPENDENCE ON EPITHELIAL MESENCHYMAL INTERACTIONS
    AUFDERHEIDE, E
    EKBLOM, P
    [J]. JOURNAL OF CELL BIOLOGY, 1988, 107 (06) : 2341 - 2349
  • [4] EPITHELIAL MESENCHYMAL INTERACTIONS IN THE DEVELOPING KIDNEY LEAD TO EXPRESSION OF TENASCIN IN THE MESENCHYME
    AUFDERHEIDE, E
    CHIQUETEHRISMANN, R
    EKBLOM, P
    [J]. JOURNAL OF CELL BIOLOGY, 1987, 105 (01) : 599 - 608
  • [5] MONOCLONAL-ANTIBODIES IN THE ANALYSIS OF FIBRONECTIN ISOFORMS GENERATED BY ALTERNATIVE SPLICING OF MESSENGER-RNA PRECURSORS IN NORMAL AND TRANSFORMED HUMAN-CELLS
    BORSI, L
    CARNEMOLLA, B
    CASTELLANI, P
    ROSELLINI, C
    VECCHIO, D
    ALLEMANNI, G
    CHANG, SE
    TAYLORPAPADIMITRIOU, J
    PANDE, H
    ZARDI, L
    [J]. JOURNAL OF CELL BIOLOGY, 1987, 104 (03) : 595 - 600
  • [6] BOURDON MA, 1983, CANCER RES, V43, P2796
  • [7] A TUMOR-ASSOCIATED FIBRONECTIN ISOFORM GENERATED BY ALTERNATIVE SPLICING OF MESSENGER-RNA PRECURSORS
    CARNEMOLLA, B
    BALZA, E
    SIRI, A
    ZARDI, L
    NICOTRA, MR
    BIGOTTI, A
    NATALI, PG
    [J]. JOURNAL OF CELL BIOLOGY, 1989, 108 (03) : 1139 - 1148
  • [8] TRANSFORMED HUMAN-CELLS RELEASE DIFFERENT FIBRONECTIN VARIANTS THAN DO NORMAL-CELLS
    CASTELLANI, P
    SIRI, A
    ROSELLINI, C
    INFUSINI, E
    BORSI, L
    ZARDI, L
    [J]. JOURNAL OF CELL BIOLOGY, 1986, 103 (05) : 1671 - 1677
  • [9] THE HUMAN PLACENTA - A MODEL FOR TENASCIN EXPRESSION
    CASTELLUCCI, M
    CLASSENLINKE, I
    MUHLHAUSER, J
    KAUFMANN, P
    ZARDI, L
    CHIQUETEHRISMANN, R
    [J]. HISTOCHEMISTRY, 1991, 95 (05) : 449 - 458
  • [10] CHICK MYOTENDINOUS ANTIGEN .2. A NOVEL EXTRACELLULAR GLYCOPROTEIN COMPLEX CONSISTING OF LARGE DISULFIDE-LINKED SUBUNITS
    CHIQUET, M
    FAMBROUGH, DM
    [J]. JOURNAL OF CELL BIOLOGY, 1984, 98 (06) : 1937 - 1946