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Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus

Daily regulation of Ca(2+)– and voltage-activated BK K(+) channel activity is required for action potential rhythmicity in the suprachiasmatic nucleus (SCN) of the hypothalamus, the brain's circadian clock. In SCN neurons, BK activation is dependent upon multiple types of Ca(2+) channels in a c...

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Autores principales: McNally, Beth A., Plante, Amber E., Meredith, Andrea L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505962/
https://www.ncbi.nlm.nih.gov/pubmed/34650447
http://dx.doi.org/10.3389/fphys.2021.737291
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author McNally, Beth A.
Plante, Amber E.
Meredith, Andrea L.
author_facet McNally, Beth A.
Plante, Amber E.
Meredith, Andrea L.
author_sort McNally, Beth A.
collection PubMed
description Daily regulation of Ca(2+)– and voltage-activated BK K(+) channel activity is required for action potential rhythmicity in the suprachiasmatic nucleus (SCN) of the hypothalamus, the brain's circadian clock. In SCN neurons, BK activation is dependent upon multiple types of Ca(2+) channels in a circadian manner. Daytime BK current predominantly requires Ca(2+) influx through L-type Ca(2+) channels (LTCCs), a time when BK channels are closely coupled with their Ca(2+) source. Here we show that daytime BK current is resistant to the Ca(2+) chelator BAPTA. However, at night when LTCCs contribute little to BK activation, BK current decreases by a third in BAPTA compared to control EGTA conditions. In phase with this time-of-day specific effect on BK current activation, LTCC current is larger during the day. The specific Ca(2+) channel subtypes underlying the LTCC current in SCN, as well as the subtypes contributing the Ca(2+) influx relevant for BK current activation, have not been identified. SCN neurons express two LTCC subtypes, Ca(V)1.2 and Ca(V)1.3. While a role for Ca(V)1.2 channels has been identified during the night, Ca(V)1.3 channel modulation has also been suggested to contribute to daytime SCN action potential activity, as well as subthreshold Ca(2+) oscillations. Here we characterize the role of Ca(V)1.3 channels in LTCC and BK current activation in SCN neurons using a global deletion of CACNA1D in mouse (Ca(V)1.3 KO). Ca(V)1.3 KO SCN neurons had a 50% reduction in the daytime LTCC current, but not total Ca(2+) current, with no difference in Ca(2+) current levels at night. During the day, Ca(V)1.3 KO neurons exhibited oscillations in membrane potential, and most neurons, although not all, also had BK currents. Changes in BK current activation were only detectable at the highest voltage tested. These data show that while Ca(V)1.3 channels contribute to the daytime Ca(2+) current, this does not translate into a major effect on the daytime BK current. These data suggest that BK current activation does not absolutely require Ca(V)1.3 channels and may therefore also depend on other LTCC subtypes, such as Ca(V)1.2.
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spelling pubmed-85059622021-10-13 Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus McNally, Beth A. Plante, Amber E. Meredith, Andrea L. Front Physiol Physiology Daily regulation of Ca(2+)– and voltage-activated BK K(+) channel activity is required for action potential rhythmicity in the suprachiasmatic nucleus (SCN) of the hypothalamus, the brain's circadian clock. In SCN neurons, BK activation is dependent upon multiple types of Ca(2+) channels in a circadian manner. Daytime BK current predominantly requires Ca(2+) influx through L-type Ca(2+) channels (LTCCs), a time when BK channels are closely coupled with their Ca(2+) source. Here we show that daytime BK current is resistant to the Ca(2+) chelator BAPTA. However, at night when LTCCs contribute little to BK activation, BK current decreases by a third in BAPTA compared to control EGTA conditions. In phase with this time-of-day specific effect on BK current activation, LTCC current is larger during the day. The specific Ca(2+) channel subtypes underlying the LTCC current in SCN, as well as the subtypes contributing the Ca(2+) influx relevant for BK current activation, have not been identified. SCN neurons express two LTCC subtypes, Ca(V)1.2 and Ca(V)1.3. While a role for Ca(V)1.2 channels has been identified during the night, Ca(V)1.3 channel modulation has also been suggested to contribute to daytime SCN action potential activity, as well as subthreshold Ca(2+) oscillations. Here we characterize the role of Ca(V)1.3 channels in LTCC and BK current activation in SCN neurons using a global deletion of CACNA1D in mouse (Ca(V)1.3 KO). Ca(V)1.3 KO SCN neurons had a 50% reduction in the daytime LTCC current, but not total Ca(2+) current, with no difference in Ca(2+) current levels at night. During the day, Ca(V)1.3 KO neurons exhibited oscillations in membrane potential, and most neurons, although not all, also had BK currents. Changes in BK current activation were only detectable at the highest voltage tested. These data show that while Ca(V)1.3 channels contribute to the daytime Ca(2+) current, this does not translate into a major effect on the daytime BK current. These data suggest that BK current activation does not absolutely require Ca(V)1.3 channels and may therefore also depend on other LTCC subtypes, such as Ca(V)1.2. Frontiers Media S.A. 2021-09-28 /pmc/articles/PMC8505962/ /pubmed/34650447 http://dx.doi.org/10.3389/fphys.2021.737291 Text en Copyright © 2021 McNally, Plante and Meredith. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
McNally, Beth A.
Plante, Amber E.
Meredith, Andrea L.
Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus
title Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus
title_full Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus
title_fullStr Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus
title_full_unstemmed Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus
title_short Contributions of Ca(V)1.3 Channels to Ca(2+) Current and Ca(2+)-Activated BK Current in the Suprachiasmatic Nucleus
title_sort contributions of ca(v)1.3 channels to ca(2+) current and ca(2+)-activated bk current in the suprachiasmatic nucleus
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505962/
https://www.ncbi.nlm.nih.gov/pubmed/34650447
http://dx.doi.org/10.3389/fphys.2021.737291
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