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Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells

The sinoatrial node (SAN) and subsidiary pacemakers in the cardiac conduction system generate spontaneous electrical activity which is indispensable for electrical and therefore contractile function of the heart. The hyperpolarisation-activated cyclic nucleotide-gated channel HCN4 is responsible for...

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Autores principales: Congreve, Samitha Dilini, Main, Alice, Butler, Andrew S., Gao, Xing, Brown, Elaine, Du, Chunyun, Choisy, Stephanié C., Cheng, Hongwei, Hancox, Jules C., Fuller, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133559/
https://www.ncbi.nlm.nih.gov/pubmed/37123274
http://dx.doi.org/10.3389/fphys.2023.1163339
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author Congreve, Samitha Dilini
Main, Alice
Butler, Andrew S.
Gao, Xing
Brown, Elaine
Du, Chunyun
Choisy, Stephanié C.
Cheng, Hongwei
Hancox, Jules C.
Fuller, William
author_facet Congreve, Samitha Dilini
Main, Alice
Butler, Andrew S.
Gao, Xing
Brown, Elaine
Du, Chunyun
Choisy, Stephanié C.
Cheng, Hongwei
Hancox, Jules C.
Fuller, William
author_sort Congreve, Samitha Dilini
collection PubMed
description The sinoatrial node (SAN) and subsidiary pacemakers in the cardiac conduction system generate spontaneous electrical activity which is indispensable for electrical and therefore contractile function of the heart. The hyperpolarisation-activated cyclic nucleotide-gated channel HCN4 is responsible for genesis of the pacemaker “funny” current during diastolic depolarisation. S-palmitoylation, the reversible conjugation of the fatty acid palmitate to protein cysteine sulfhydryls, regulates the activity of key cardiac Na(+) and Ca(2+) handling proteins, influencing their membrane microdomain localisation and function. We investigated HCN4 palmitoylation and its functional consequences in engineered human embryonic kidney 293T cells as well as endogenous HCN4 in neonatal rat ventricular myocytes. HCN4 was palmitoylated in all experimental systems investigated. We mapped the HCN4 palmitoylation sites to a pair of cysteines in the HCN4 intracellular amino terminus. A double cysteine-to-alanine mutation CC93A/179AA of full length HCN4 caused a ∼67% reduction in palmitoylation in comparison to wild type HCN4. We used whole-cell patch clamp to evaluate HCN4 current (I(HCN4)) in stably transfected 293T cells. Removal of the two N-terminal palmitoylation sites did not significantly alter half maximal activation voltage of I(HCN4) or the activation slope factor. I(HCN4) was significantly larger in cells expressing wild type compared to non-palmitoylated HCN4 across a range of voltages. Phylogenetic analysis revealed that although cysteine 93 is widely conserved across all classes of HCN4 vertebrate orthologs, conservation of cysteine 179 is restricted to placental mammals. Collectively, we provide evidence for functional regulation of HCN4 via palmitoylation of its amino terminus in vertebrates. We suggest that by recruiting the amino terminus to the bilayer, palmitoylation enhances the magnitude of HCN4-mediated currents, but does not significantly affect the kinetics.
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spelling pubmed-101335592023-04-28 Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells Congreve, Samitha Dilini Main, Alice Butler, Andrew S. Gao, Xing Brown, Elaine Du, Chunyun Choisy, Stephanié C. Cheng, Hongwei Hancox, Jules C. Fuller, William Front Physiol Physiology The sinoatrial node (SAN) and subsidiary pacemakers in the cardiac conduction system generate spontaneous electrical activity which is indispensable for electrical and therefore contractile function of the heart. The hyperpolarisation-activated cyclic nucleotide-gated channel HCN4 is responsible for genesis of the pacemaker “funny” current during diastolic depolarisation. S-palmitoylation, the reversible conjugation of the fatty acid palmitate to protein cysteine sulfhydryls, regulates the activity of key cardiac Na(+) and Ca(2+) handling proteins, influencing their membrane microdomain localisation and function. We investigated HCN4 palmitoylation and its functional consequences in engineered human embryonic kidney 293T cells as well as endogenous HCN4 in neonatal rat ventricular myocytes. HCN4 was palmitoylated in all experimental systems investigated. We mapped the HCN4 palmitoylation sites to a pair of cysteines in the HCN4 intracellular amino terminus. A double cysteine-to-alanine mutation CC93A/179AA of full length HCN4 caused a ∼67% reduction in palmitoylation in comparison to wild type HCN4. We used whole-cell patch clamp to evaluate HCN4 current (I(HCN4)) in stably transfected 293T cells. Removal of the two N-terminal palmitoylation sites did not significantly alter half maximal activation voltage of I(HCN4) or the activation slope factor. I(HCN4) was significantly larger in cells expressing wild type compared to non-palmitoylated HCN4 across a range of voltages. Phylogenetic analysis revealed that although cysteine 93 is widely conserved across all classes of HCN4 vertebrate orthologs, conservation of cysteine 179 is restricted to placental mammals. Collectively, we provide evidence for functional regulation of HCN4 via palmitoylation of its amino terminus in vertebrates. We suggest that by recruiting the amino terminus to the bilayer, palmitoylation enhances the magnitude of HCN4-mediated currents, but does not significantly affect the kinetics. Frontiers Media S.A. 2023-04-13 /pmc/articles/PMC10133559/ /pubmed/37123274 http://dx.doi.org/10.3389/fphys.2023.1163339 Text en Copyright © 2023 Congreve, Main, Butler, Gao, Brown, Du, Choisy, Cheng, Hancox and Fuller. 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
Congreve, Samitha Dilini
Main, Alice
Butler, Andrew S.
Gao, Xing
Brown, Elaine
Du, Chunyun
Choisy, Stephanié C.
Cheng, Hongwei
Hancox, Jules C.
Fuller, William
Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells
title Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells
title_full Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells
title_fullStr Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells
title_full_unstemmed Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells
title_short Palmitoylation regulates the magnitude of HCN4-mediated currents in mammalian cells
title_sort palmitoylation regulates the magnitude of hcn4-mediated currents in mammalian cells
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133559/
https://www.ncbi.nlm.nih.gov/pubmed/37123274
http://dx.doi.org/10.3389/fphys.2023.1163339
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