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A cation counterflux supports lysosomal acidification
The profound luminal acidification essential for the degradative function of lysosomes requires a counter-ion flux to dissipate an opposing voltage that would prohibit proton accumulation. It has generally been assumed that a parallel anion influx is the main or only counter-ion transport that enabl...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2894458/ https://www.ncbi.nlm.nih.gov/pubmed/20566682 http://dx.doi.org/10.1083/jcb.200911083 |
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author | Steinberg, Benjamin E. Huynh, Kassidy K. Brodovitch, Alexandre Jabs, Sabrina Stauber, Tobias Jentsch, Thomas J. Grinstein, Sergio |
author_facet | Steinberg, Benjamin E. Huynh, Kassidy K. Brodovitch, Alexandre Jabs, Sabrina Stauber, Tobias Jentsch, Thomas J. Grinstein, Sergio |
author_sort | Steinberg, Benjamin E. |
collection | PubMed |
description | The profound luminal acidification essential for the degradative function of lysosomes requires a counter-ion flux to dissipate an opposing voltage that would prohibit proton accumulation. It has generally been assumed that a parallel anion influx is the main or only counter-ion transport that enables acidification. Indeed, defective anion conductance has been suggested as the mechanism underlying attenuated lysosome acidification in cells deficient in CFTR or ClC-7. To assess the individual contribution of counter-ions to acidification, we devised means of reversibly and separately permeabilizing the plasma and lysosomal membranes to dialyze the cytosol and lysosome lumen in intact cells, while ratiometrically monitoring lysosomal pH. Replacement of cytosolic Cl(−) with impermeant anions did not significantly alter proton pumping, while the presence of permeant cations in the lysosomal lumen supported acidification. Accordingly, the lysosomes were found to acidify to the same pH in both CFTR- and ClC-7–deficient cells. We conclude that cations, in addition to chloride, can support lysosomal acidification and defects in lysosomal anion conductance cannot explain the impaired microbicidal capacity of CF phagocytes. |
format | Text |
id | pubmed-2894458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28944582010-12-28 A cation counterflux supports lysosomal acidification Steinberg, Benjamin E. Huynh, Kassidy K. Brodovitch, Alexandre Jabs, Sabrina Stauber, Tobias Jentsch, Thomas J. Grinstein, Sergio J Cell Biol Research Articles The profound luminal acidification essential for the degradative function of lysosomes requires a counter-ion flux to dissipate an opposing voltage that would prohibit proton accumulation. It has generally been assumed that a parallel anion influx is the main or only counter-ion transport that enables acidification. Indeed, defective anion conductance has been suggested as the mechanism underlying attenuated lysosome acidification in cells deficient in CFTR or ClC-7. To assess the individual contribution of counter-ions to acidification, we devised means of reversibly and separately permeabilizing the plasma and lysosomal membranes to dialyze the cytosol and lysosome lumen in intact cells, while ratiometrically monitoring lysosomal pH. Replacement of cytosolic Cl(−) with impermeant anions did not significantly alter proton pumping, while the presence of permeant cations in the lysosomal lumen supported acidification. Accordingly, the lysosomes were found to acidify to the same pH in both CFTR- and ClC-7–deficient cells. We conclude that cations, in addition to chloride, can support lysosomal acidification and defects in lysosomal anion conductance cannot explain the impaired microbicidal capacity of CF phagocytes. The Rockefeller University Press 2010-06-28 /pmc/articles/PMC2894458/ /pubmed/20566682 http://dx.doi.org/10.1083/jcb.200911083 Text en © 2010 Steinberg et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Steinberg, Benjamin E. Huynh, Kassidy K. Brodovitch, Alexandre Jabs, Sabrina Stauber, Tobias Jentsch, Thomas J. Grinstein, Sergio A cation counterflux supports lysosomal acidification |
title | A cation counterflux supports lysosomal acidification |
title_full | A cation counterflux supports lysosomal acidification |
title_fullStr | A cation counterflux supports lysosomal acidification |
title_full_unstemmed | A cation counterflux supports lysosomal acidification |
title_short | A cation counterflux supports lysosomal acidification |
title_sort | cation counterflux supports lysosomal acidification |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2894458/ https://www.ncbi.nlm.nih.gov/pubmed/20566682 http://dx.doi.org/10.1083/jcb.200911083 |
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