Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.

Central nervous system nicotinic acetylcholine receptors (nAChR) are predominantly of the α4β2 subtype. Two isoforms exist, with high or low agonist sensitivity (HS-(α4β2)2β2- and LS-(α4β2)2α4-nAChR). Both isoforms exhibit similar macroscopic potency and efficacy values at low acetylcholine (ACh) co...

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Main Authors: Maegan M Weltzin, Andrew A George, Ronald J Lukas, Paul Whiteaker
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0213143
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spelling doaj-36f443dad2634fd983f3d824b9e6f38f2021-03-03T20:50:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01143e021314310.1371/journal.pone.0213143Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.Maegan M WeltzinAndrew A GeorgeRonald J LukasPaul WhiteakerCentral nervous system nicotinic acetylcholine receptors (nAChR) are predominantly of the α4β2 subtype. Two isoforms exist, with high or low agonist sensitivity (HS-(α4β2)2β2- and LS-(α4β2)2α4-nAChR). Both isoforms exhibit similar macroscopic potency and efficacy values at low acetylcholine (ACh) concentrations, mediated by a common pair of high-affinity α4(+)/(-)β2 subunit binding interfaces. However LS-(α4β2)2α4-nAChR also respond to higher concentrations of ACh, acting at a third α4(+)/(-)α4 subunit interface. To probe isoform functional differences further, HS- and LS-α4β2-nAChR were expressed in Xenopus laevis oocytes and single-channel responses were assessed using cell-attached patch-clamp. In the presence of a low ACh concentration, both isoforms produce low-bursting function. HS-(α4β2)2β2-nAChR exhibit a single conductance state, whereas LS-(α4β2)2α4-nAChR display two distinctive conductance states. A higher ACh concentration did not preferentially recruit either conductance state, but did result in increased LS-(α4β2)2α4-nAChR bursting and reduced closed times. Introduction of an α4(+)/(-)α4-interface loss-of-function α4W182A mutation abolished these changes, confirming this site's role in mediating LS-(α4β2)2α4-nAChR responses. Small or large amplitude openings are highly-correlated within individual LS-(α4β2)2α4-nAChR bursts, suggesting that they arise from distinct intermediate states, each of which is stabilized by α4(+)/(-)α4 site ACh binding. These findings are consistent with α4(+)/(-)α4 subunit interface occupation resulting in allosteric potentiation of agonist actions at α4(+)/(-)β2 subunit interfaces, rather than independent induction of high conductance channel openings.https://doi.org/10.1371/journal.pone.0213143
collection DOAJ
language English
format Article
sources DOAJ
author Maegan M Weltzin
Andrew A George
Ronald J Lukas
Paul Whiteaker
spellingShingle Maegan M Weltzin
Andrew A George
Ronald J Lukas
Paul Whiteaker
Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.
PLoS ONE
author_facet Maegan M Weltzin
Andrew A George
Ronald J Lukas
Paul Whiteaker
author_sort Maegan M Weltzin
title Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.
title_short Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.
title_full Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.
title_fullStr Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.
title_full_unstemmed Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.
title_sort distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Central nervous system nicotinic acetylcholine receptors (nAChR) are predominantly of the α4β2 subtype. Two isoforms exist, with high or low agonist sensitivity (HS-(α4β2)2β2- and LS-(α4β2)2α4-nAChR). Both isoforms exhibit similar macroscopic potency and efficacy values at low acetylcholine (ACh) concentrations, mediated by a common pair of high-affinity α4(+)/(-)β2 subunit binding interfaces. However LS-(α4β2)2α4-nAChR also respond to higher concentrations of ACh, acting at a third α4(+)/(-)α4 subunit interface. To probe isoform functional differences further, HS- and LS-α4β2-nAChR were expressed in Xenopus laevis oocytes and single-channel responses were assessed using cell-attached patch-clamp. In the presence of a low ACh concentration, both isoforms produce low-bursting function. HS-(α4β2)2β2-nAChR exhibit a single conductance state, whereas LS-(α4β2)2α4-nAChR display two distinctive conductance states. A higher ACh concentration did not preferentially recruit either conductance state, but did result in increased LS-(α4β2)2α4-nAChR bursting and reduced closed times. Introduction of an α4(+)/(-)α4-interface loss-of-function α4W182A mutation abolished these changes, confirming this site's role in mediating LS-(α4β2)2α4-nAChR responses. Small or large amplitude openings are highly-correlated within individual LS-(α4β2)2α4-nAChR bursts, suggesting that they arise from distinct intermediate states, each of which is stabilized by α4(+)/(-)α4 site ACh binding. These findings are consistent with α4(+)/(-)α4 subunit interface occupation resulting in allosteric potentiation of agonist actions at α4(+)/(-)β2 subunit interfaces, rather than independent induction of high conductance channel openings.
url https://doi.org/10.1371/journal.pone.0213143
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