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Acidic pH is essential for maintaining mast cell secretory granule homeostasis
It has been recognized for a long time that the secretory granules of mast cells are acidic, but the functional importance of maintaining an acidic pH in the mast cell granules is not fully understood. Here we addressed this issue by examining the effects of raising the pH of the mast cell secretory...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584528/ https://www.ncbi.nlm.nih.gov/pubmed/28492555 http://dx.doi.org/10.1038/cddis.2017.206 |
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author | Pejler, Gunnar Hu Frisk, Jun Mei Sjöström, Daniel Paivandy, Aida Öhrvik, Helena |
author_facet | Pejler, Gunnar Hu Frisk, Jun Mei Sjöström, Daniel Paivandy, Aida Öhrvik, Helena |
author_sort | Pejler, Gunnar |
collection | PubMed |
description | It has been recognized for a long time that the secretory granules of mast cells are acidic, but the functional importance of maintaining an acidic pH in the mast cell granules is not fully understood. Here we addressed this issue by examining the effects of raising the pH of the mast cell secretory granules. Mast cells were incubated with bafilomycin A1, an inhibitor of the vacuolar-type ATPase proton pump. Supporting a role of vacuolar-type ATPase in mast cell granule acidification, bafilomycin A1 treatment caused a robust increase in granule pH. This was accompanied by marked effects on mast cell granules, including swelling and acquisition of vacuole-like morphology. Moreover, bafilomycin A1 caused extensive, yet selective effects on the granule content. These included aberrant processing of pro-carboxypeptidase A3 and a reduction in the level of intracellular histamine, the latter being accompanied by an increase in extracellular histamine. In contrast, the storage of β-hexosaminidase, a prototype lysosomal hydrolase known to be stored in mast cell granules, was not affected by abrogation of granule acidification. Moreover, bafilomycin A1 caused a reduction of tryptase enzymatic activity and appearance of tryptase degradation products. Tryptase inhibition prevented the formation of such degradation products, suggesting that the pH elevation causes tryptase to undergo autoproteolysis. Taken together, our findings reveal that mast cell secretory granule homeostasis is critically dependent on an acidic milieu. |
format | Online Article Text |
id | pubmed-5584528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55845282017-09-06 Acidic pH is essential for maintaining mast cell secretory granule homeostasis Pejler, Gunnar Hu Frisk, Jun Mei Sjöström, Daniel Paivandy, Aida Öhrvik, Helena Cell Death Dis Original Article It has been recognized for a long time that the secretory granules of mast cells are acidic, but the functional importance of maintaining an acidic pH in the mast cell granules is not fully understood. Here we addressed this issue by examining the effects of raising the pH of the mast cell secretory granules. Mast cells were incubated with bafilomycin A1, an inhibitor of the vacuolar-type ATPase proton pump. Supporting a role of vacuolar-type ATPase in mast cell granule acidification, bafilomycin A1 treatment caused a robust increase in granule pH. This was accompanied by marked effects on mast cell granules, including swelling and acquisition of vacuole-like morphology. Moreover, bafilomycin A1 caused extensive, yet selective effects on the granule content. These included aberrant processing of pro-carboxypeptidase A3 and a reduction in the level of intracellular histamine, the latter being accompanied by an increase in extracellular histamine. In contrast, the storage of β-hexosaminidase, a prototype lysosomal hydrolase known to be stored in mast cell granules, was not affected by abrogation of granule acidification. Moreover, bafilomycin A1 caused a reduction of tryptase enzymatic activity and appearance of tryptase degradation products. Tryptase inhibition prevented the formation of such degradation products, suggesting that the pH elevation causes tryptase to undergo autoproteolysis. Taken together, our findings reveal that mast cell secretory granule homeostasis is critically dependent on an acidic milieu. Nature Publishing Group 2017-05-11 /pmc/articles/PMC5584528/ /pubmed/28492555 http://dx.doi.org/10.1038/cddis.2017.206 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Pejler, Gunnar Hu Frisk, Jun Mei Sjöström, Daniel Paivandy, Aida Öhrvik, Helena Acidic pH is essential for maintaining mast cell secretory granule homeostasis |
title | Acidic pH is essential for maintaining mast cell secretory granule homeostasis |
title_full | Acidic pH is essential for maintaining mast cell secretory granule homeostasis |
title_fullStr | Acidic pH is essential for maintaining mast cell secretory granule homeostasis |
title_full_unstemmed | Acidic pH is essential for maintaining mast cell secretory granule homeostasis |
title_short | Acidic pH is essential for maintaining mast cell secretory granule homeostasis |
title_sort | acidic ph is essential for maintaining mast cell secretory granule homeostasis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584528/ https://www.ncbi.nlm.nih.gov/pubmed/28492555 http://dx.doi.org/10.1038/cddis.2017.206 |
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