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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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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