Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 98, Issue 6, Pages 3501-3506Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.051622798
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- NIDA NIH HHS [P50 DA005010, DA11836] Funding Source: Medline
- NIDCD NIH HHS [DC02871] Funding Source: Medline
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We report the cloning and characterization of rat alpha 10, a previously unidentified member of the nicotinic acetylcholine receptor (nAChR) subunit gene family. The protein encoded by the alpha 10 nAChR subunit gene is most similar to the rat alpha9 nAChR, and both alpha9 and alpha 10 subunit genes are transcribed in adult rat mechanosensory hair cells. Injection of Xenopus laevis oocytes with alpha 10 cRNA alone or in pairwise combinations with either alpha2-alpha6 or beta2-beta4 subunit cRNAs yielded no detectable ACh-gated currents. However, coinjection of alpha9 and alpha 10 cRNAs resulted in the appearance of an unusual nAChR subtype, Compared with homomeric alpha9 channels, the alpha9 alpha 10 nAChR subtype displays faster and more extensive agonist-mediated desensitization, a distinct current-voltage relationship, and a biphasic response to changes in extracellular Ca2+ ions, The pharmacological profiles of homomeric alpha9 and heteromeric alpha9 alpha 10 nAChRs are essentially indistinguishable and closely resemble those reported for endogenous cholinergic eceptors found in vertebrate hair cells, Our data suggest that efferent modulation of hair cell function occurs, at least in part, through heteromeric nAChRs assembled from both alpha9 and alpha 10 subunits.
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