The expression of tenascin-C with the AD1 variable repeat in embryonic tissues, cell lines and tumors in various vertebrate species

被引:38
作者
Derr, LB
ChiquetEhrismann, R
GandourEdwards, R
Spence, J
Tucker, RP
机构
[1] UNIV CALIF DAVIS,DEPT CELL BIOL & HUMAN ANAT,DAVIS,CA 95616
[2] BOWMAN GRAY SCH MED,DEPT ANAT & NEUROBIOL,WINSTON SALEM,NC 27510
[3] BOWMAN GRAY SCH MED,DEPT DERMATOL,WINSTON SALEM,NC 27510
[4] FRIEDRICH MIESCHER INST,CH-4002 BASEL,SWITZERLAND
[5] UNIV CALIF DAVIS,DEPT MED PATHOL,DAVIS,CA 95616
关键词
D O I
10.1046/j.1432-0436.1997.6220071.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tenascin-C is a modular glycoprotein composed of domains of amino acid repeats. All forms of tenascin-C have eight constant fibronectin type III repeats, but additional fibronectin type LU repeats can be spliced into a variable domain found between the fifth and sixth constant repeats. Four extra repeats, named A, B, C and D, have been examined previously. Here, we have used in situ hybridization to determine the tissue origins of the navel AD1 and AD2 repeats. In the embryonic-day-10 chicken embryo, transcripts encoding the AD2 repeat are limited to the tips of lung bronchioles and the base of feather buds. In contrast the AD1 hybridization signal was widespread. Quantitative in situ hybridization reveals AD1-containing transcripts represent up to 85% of the total tenascin-C mRNA in some tissues (developing bone), and are undetectable in others (e.g. radial glia). Avian and human tumor cell lines were examined for the expression of the ADI repeat using the reverse transcriptase polymerase chain-reaction (RT-PCR). Transcripts encoding six different tenascin-C splice variants incorporating the ADI repeat were found in the fibrosarcoma cell line, QT6. Many human tumor cells, including malignant melanoma and ductal breast carcinoma, were positive for AD1 tenascin-C expression. In addition, we found evidence of AD1 tenascin-C expression in samples of excised human tumors. Our results show that a novel variant may be a major part of the tenascin-C of the embryonic extracellular matrix, and may also be found in the stroma surrounding some human tumors.
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页码:71 / 82
页数:12
相关论文
共 39 条
[1]  
AUKHIL I, 1993, J BIOL CHEM, V268, P2542
[2]   EXPRESSION OF DIFFERENT TENASCIN ISOFORMS IN NORMAL, HYPERPLASTIC AND NEOPLASTIC HUMAN BREAST TISSUES [J].
BORSI, L ;
CARNEMOLLA, B ;
NICOLO, G ;
SPINA, B ;
TANARA, G ;
ZARDI, L .
INTERNATIONAL JOURNAL OF CANCER, 1992, 52 (05) :688-692
[3]   COMPARISON OF HUMAN TENASCIN EXPRESSION IN NORMAL, SIMIAN-VIRUS-40-TRANSFORMED AND TUMOR-DERIVED CELL-LINES [J].
CARNEMOLLA, B ;
BORSI, L ;
BANNIKOV, G ;
TROYANOVSKY, S ;
ZARDI, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 205 (02) :561-567
[4]   CHICK MYOTENDINOUS ANTIGEN .1. A MONOCLONAL-ANTIBODY AS A MARKER FOR TENDON AND MUSCLE MORPHOGENESIS [J].
CHIQUET, M ;
FAMBROUGH, DM .
JOURNAL OF CELL BIOLOGY, 1984, 98 (06) :1926-1936
[5]   TENASCIN VARIANTS - DIFFERENTIAL BINDING TO FIBRONECTIN AND DISTINCT DISTRIBUTION IN CELL-CULTURES AND TISSUES [J].
CHIQUETEHRISMANN, R ;
MATSUOKA, Y ;
HOFER, U ;
SPRING, J ;
BERNASCONI, C ;
CHIQUET, M .
CELL REGULATION, 1991, 2 (11) :927-938
[6]  
CHIQUETEHRISMANN R, 1993, SEMIN CANCER BIOL, V4, P301
[7]   TENASCIN - AN EXTRACELLULAR-MATRIX PROTEIN INVOLVED IN TISSUE INTERACTIONS DURING FETAL DEVELOPMENT AND ONCOGENESIS [J].
CHIQUETEHRISMANN, R ;
MACKIE, EJ ;
PEARSON, CA ;
SAKAKURA, T .
CELL, 1986, 47 (01) :131-139
[8]   TENASCIN INTERFERES WITH FIBRONECTIN ACTION [J].
CHIQUETEHRISMANN, R ;
KALLA, P ;
PEARSON, CA ;
BECK, K ;
CHIQUET, M .
CELL, 1988, 53 (03) :383-390
[9]   Mitogenesis, cell migration, and loss of focal adhesions induced by tenascin-C interacting with its cell surface receptor, annexin II [J].
Chung, CY ;
MurphyUllrich, JE ;
Erickson, HP .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (06) :883-892
[10]   CELL-SURFACE ANNEXIN-II IS A HIGH-AFFINITY RECEPTOR FOR THE ALTERNATIVELY SPLICED SEGMENT OF TENASCIN-C [J].
CHUNG, CY ;
ERICKSON, HP .
JOURNAL OF CELL BIOLOGY, 1994, 126 (02) :539-548