Functional contributions of alpha 5 subunit to neuronal acetylcholine receptor channels

被引:322
作者
RamirezLatorre, J
Yu, CR
Qu, X
Perin, F
Karlin, A
Role, L
机构
[1] COLUMBIA UNIV COLL PHYS & SURG,CTR NEUROBIOL & BEHAV,DEPT ANAT & CELL BIOL,NEW YORK,NY 10032
[2] COLUMBIA UNIV COLL PHYS & SURG,ECOLE NORMALE SUPER,NEW YORK,NY 10032
[3] COLUMBIA UNIV COLL PHYS & SURG,CTR MOL RECOGNIT,NEW YORK,NY 10032
关键词
D O I
10.1038/380347a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
LIGAND-GATED ion channels are multi-subunit complexes where each subunit-type is encoded by several related genes. Heterologous expression of any one of the neuronal nicotinic acetylcholine receptors (nAChR) alpha-type subunits, either alone or with any beta-type subunit, typically yields functional nAChR channels(1-5). A striking exception is the nAChR alpha 5 subunit: although apparently complexed with beta 2 and beta 4 nAChR subunits in neurons(6-8), and expressed in a subset of neurons within the central and peripheral nervous systems(9,10), heterologous expression of alpha 5, either alone or with any beta-type subunit has failed to yield functional channels(1.11). We demonstrate here that alpha 5 does participate in nAChRs expressed in heterologous systems and in primary neurons, and further that alpha 5 contributes to the lining of functionally unique nAChR channels, but only if coexpressed with both another alpha- and beta-type subunit. Furthermore, channels containing the alpha 5 subunit are potently activated and desensitized by nanomolar concentrations of nicotine.
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页码:347 / 351
页数:5
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