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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2017
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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. |
format | Online Article Text |
id | pubmed-5461029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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