TY - JOUR
T1 - The coxsackievirus-adenovirus receptor protein as a cell adhesion molecule in the developing mouse brain
AU - Honda, Takao
AU - Saitoh, Hiroshi
AU - Masuko, Masayoshi
AU - Katagiri-Abe, Takako
AU - Tominaga, Kei
AU - Kozakai, Ikuo
AU - Kobayashi, Kazuo
AU - Kumanishi, Toshiro
AU - Watanabe, Yuichi G.
AU - Odani, Shoji
AU - Kuwano, Ryozo
N1 - Funding Information:
We thank Drs Tadahiro Hamada and Akiko Nishiyama for the helpful discussions, and Dr Hiroaki Asou for the valuable comments on the aggregation assay. This work was supported in part by Grants-in-Aid from the Ministry of Education, Science, Sports, and Culture, and the Ministry of Health and Welfare of Japan (to RK).
PY - 2000/4/14
Y1 - 2000/4/14
N2 - 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 B.V.
AB - 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 B.V.
KW - Adhesion molecule
KW - Coxsackievirus and adenovirus receptor
KW - In situ hybridization
KW - Nerve growth cone
KW - Subcellular localization
UR - http://www.scopus.com/inward/record.url?scp=0034646786&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034646786&partnerID=8YFLogxK
U2 - 10.1016/S0169-328X(00)00036-X
DO - 10.1016/S0169-328X(00)00036-X
M3 - Article
C2 - 10814828
AN - SCOPUS:0034646786
SN - 0169-328X
VL - 77
SP - 19
EP - 28
JO - Molecular Brain Research
JF - Molecular Brain Research
IS - 1
ER -