The coxsackievirus-adenovirus receptor protein as a cell adhesion molecule in the developing mouse brain

被引:195
作者
Honda, T
Saitoh, H
Masuko, M
Katagiri-Abe, T
Tominaga, K
Kozakai, I
Kobayashi, K
Kumanishi, T
Watanabe, YG
Odani, S
Kuwano, R
机构
[1] Niigata Univ, Res Lab Mol Genet, Niigata 9518510, Japan
[2] Niigata Univ, Grad Sch Sci & Technol, Course Biosyst Sci, Niigata 9502181, Japan
[3] Niigata Univ, Brain Res Inst, Niigata 9518585, Japan
来源
MOLECULAR BRAIN RESEARCH | 2000年 / 77卷 / 01期
关键词
coxsackievirus and adenovirus receptor; nerve growth cone; adhesion molecule; subcellular localization; in situ hybridization;
D O I
10.1016/S0169-328X(00)00036-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In an attempt to elucidate the molecular mechanisms underlying neuro-network formation in the developing brain, we analyzed 130 proteolytic cleavage peptides of membrane proteins purified from newborn mouse brains. We describe here the characterization of a membrane protein with an apparent molecular mass of 46 kDa, a member of the immunoglobulin superfamily of which the cDNA sequence was recently reported, encoding the mouse homologue of the human coxsackievirus and adenovirus receptor (mCAR). Western and Northern blot analyses demonstrated the abundant expression of mCAR in the mouse brain, the highest level being observed in the newborn mouse brain, and its expression was detected in embryos as early as at 10.5 days post-coitus (dpc), but decreased rapidly after birth. On in situ hybridization, mCAR mRNA expression was observed throughout the newborn mouse brain. In primary neurons from the hippocampi of mouse embryos the expression of mCAR was observed throughout the cells including those in growth cones on immunohistochemistry. In order to determine whether or not mCAR is involved in cell adhesion, aggregation assays were carried out. C6 cells transfected with mCAR cDNA aggregated homophilically, which was inhibited by specific antibodies against the extracellular domain of mCAR. In addition to its action as a virus receptor, mCAR may function naturally as an adhesion molecule involved in neuro-network formation in the developing nervous system. (C) 2000 Elsevier Science BN. All rights reserved.
引用
收藏
页码:19 / 28
页数:10
相关论文
共 25 条
[1]   The presence of the 50-kDa subunit of dynactin complex in the nerve growth cone [J].
Abe, TK ;
Tanaka, H ;
Iwanaga, T ;
Odani, S ;
Kuwano, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 233 (02) :295-299
[2]   Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5 [J].
Bergelson, JM ;
Cunningham, JA ;
Droguett, G ;
KurtJones, EA ;
Krithivas, A ;
Hong, JS ;
Horwitz, MS ;
Crowell, RL ;
Finberg, RW .
SCIENCE, 1997, 275 (5304) :1320-1323
[3]   The murine CAR homolog is a receptor for coxsackie B viruses and adenoviruses [J].
Bergelson, JM ;
Krithivas, A ;
Celi, L ;
Droguett, G ;
Horwitz, MS ;
Wickham, T ;
Crowell, RL ;
Finberg, RW .
JOURNAL OF VIROLOGY, 1998, 72 (01) :415-419
[4]   GROWTH OF A RAT NEUROBLASTOMA CELL LINE IN SERUM-FREE SUPPLEMENTED MEDIUM [J].
BOTTENSTEIN, JE ;
SATO, GH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (01) :514-517
[5]   CTX, a novel molecule specifically expressed on the surface of cortical thymocytes in Xenopus [J].
Chretien, I ;
Robert, J ;
Marcuz, A ;
GarciaSanz, JA ;
Courtet, M ;
DuPasquier, L .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (04) :780-791
[6]   AN UNIDENTIFIED, FILTRABLE AGENT ISOLATED FROM THE FECES OF CHILDREN WITH PARALYSIS [J].
DALLDORF, G ;
SICKLES, GM .
SCIENCE, 1948, 108 (2794) :61-62
[7]   DEVELOPMENTAL MECHANISMS THAT GENERATE PRECISE PATTERNS OF NEURONAL CONNECTIVITY [J].
GOODMAN, CS ;
SHATZ, CJ .
CELL, 1993, 72 :77-98
[8]  
Goslin K., 1991, CULTURING NERVE CELL, P251
[9]   The human A33 antigen is a transmembrane glycoprotein and a novel member of the immunoglobulin superfamily [J].
Heath, JK ;
White, SJ ;
Johnstone, CN ;
Catimel, B ;
Simpson, RJ ;
Moritz, RL ;
Tu, GF ;
Ji, H ;
Whitehead, RH ;
Groenen, LC ;
Scott, AM ;
Ritter, G ;
Cohen, L ;
Welt, S ;
Old, LJ ;
Nice, EC ;
Burgess, AW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) :469-474
[10]   FLUORESCENT CARBOCYANINE DYES ALLOW LIVING NEURONS OF IDENTIFIED ORIGIN TO BE STUDIED IN LONG-TERM CULTURES [J].
HONIG, MG ;
HUME, RI .
JOURNAL OF CELL BIOLOGY, 1986, 103 (01) :171-187