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A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores

The resting membrane potential (Δψ) of the cell is negative on the cytosolic side and determined primarily by the plasma membrane’s selective permeability to K(+). We show that lysosomal Δψ is set by lysosomal membrane permeabilities to Na(+) and H(+), but not K(+), and is positive on the cytosolic...

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Autores principales: Wang, Wuyang, Zhang, Xiaoli, Gao, Qiong, Lawas, Maria, Yu, Lu, Cheng, Xiping, Gu, Mingxue, Sahoo, Nirakar, Li, Xinran, Li, Ping, Ireland, Stephen, Meredith, Andrea, Xu, Haoxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461029/
https://www.ncbi.nlm.nih.gov/pubmed/28468834
http://dx.doi.org/10.1083/jcb.201612123
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author Wang, Wuyang
Zhang, Xiaoli
Gao, Qiong
Lawas, Maria
Yu, Lu
Cheng, Xiping
Gu, Mingxue
Sahoo, Nirakar
Li, Xinran
Li, Ping
Ireland, Stephen
Meredith, Andrea
Xu, Haoxing
author_facet Wang, Wuyang
Zhang, Xiaoli
Gao, Qiong
Lawas, Maria
Yu, Lu
Cheng, Xiping
Gu, Mingxue
Sahoo, Nirakar
Li, Xinran
Li, Ping
Ireland, Stephen
Meredith, Andrea
Xu, Haoxing
author_sort Wang, Wuyang
collection PubMed
description The resting membrane potential (Δψ) of the cell is negative on the cytosolic side and determined primarily by the plasma membrane’s selective permeability to K(+). We show that lysosomal Δψ is set by lysosomal membrane permeabilities to Na(+) and H(+), but not K(+), and is positive on the cytosolic side. An increase in juxta-lysosomal Ca(2+) rapidly reversed lysosomal Δψ by activating a large voltage-dependent and K(+)-selective conductance (LysoK(VCa)). LysoK(VCa) is encoded molecularly by SLO1 proteins known for forming plasma membrane BK channels. Opening of single LysoK(VCa) channels is sufficient to cause the rapid, striking changes in lysosomal Δψ. Lysosomal Ca(2+) stores may be refilled from endoplasmic reticulum (ER) Ca(2+) via ER–lysosome membrane contact sites. We propose that LysoK(VCa) serves as the perilysosomal Ca(2+) effector to prime lysosomes for the refilling process. Consistently, genetic ablation or pharmacological inhibition of LysoK(VCa), or abolition of its Ca(2+) sensitivity, blocks refilling and maintenance of lysosomal Ca(2+) stores, resulting in lysosomal cholesterol accumulation and a lysosome storage phenotype.
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spelling pubmed-54610292017-12-05 A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores Wang, Wuyang Zhang, Xiaoli Gao, Qiong Lawas, Maria Yu, Lu Cheng, Xiping Gu, Mingxue Sahoo, Nirakar Li, Xinran Li, Ping Ireland, Stephen Meredith, Andrea Xu, Haoxing J Cell Biol Research Articles The resting membrane potential (Δψ) of the cell is negative on the cytosolic side and determined primarily by the plasma membrane’s selective permeability to K(+). We show that lysosomal Δψ is set by lysosomal membrane permeabilities to Na(+) and H(+), but not K(+), and is positive on the cytosolic side. An increase in juxta-lysosomal Ca(2+) rapidly reversed lysosomal Δψ by activating a large voltage-dependent and K(+)-selective conductance (LysoK(VCa)). LysoK(VCa) is encoded molecularly by SLO1 proteins known for forming plasma membrane BK channels. Opening of single LysoK(VCa) channels is sufficient to cause the rapid, striking changes in lysosomal Δψ. Lysosomal Ca(2+) stores may be refilled from endoplasmic reticulum (ER) Ca(2+) via ER–lysosome membrane contact sites. We propose that LysoK(VCa) serves as the perilysosomal Ca(2+) effector to prime lysosomes for the refilling process. Consistently, genetic ablation or pharmacological inhibition of LysoK(VCa), or abolition of its Ca(2+) sensitivity, blocks refilling and maintenance of lysosomal Ca(2+) stores, resulting in lysosomal cholesterol accumulation and a lysosome storage phenotype. The Rockefeller University Press 2017-06-05 /pmc/articles/PMC5461029/ /pubmed/28468834 http://dx.doi.org/10.1083/jcb.201612123 Text en © 2017 Wang et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Wang, Wuyang
Zhang, Xiaoli
Gao, Qiong
Lawas, Maria
Yu, Lu
Cheng, Xiping
Gu, Mingxue
Sahoo, Nirakar
Li, Xinran
Li, Ping
Ireland, Stephen
Meredith, Andrea
Xu, Haoxing
A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores
title A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores
title_full A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores
title_fullStr A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores
title_full_unstemmed A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores
title_short A voltage-dependent K(+) channel in the lysosome is required for refilling lysosomal Ca(2+) stores
title_sort voltage-dependent k(+) channel in the lysosome is required for refilling lysosomal ca(2+) stores
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461029/
https://www.ncbi.nlm.nih.gov/pubmed/28468834
http://dx.doi.org/10.1083/jcb.201612123
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