Granule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells

Mast cells are multifunctional immune cells scattered in tissues near blood vessels and mucosal surfaces where they mediate important reactions against parasites and contribute to the pathogenesis of allergic reactions. Serine proteases released from secretory granules upon mast cell activation cont...

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Autores principales: Sabrina Sofia Burgener, Melanie Brügger, Nathan Georges François Leborgne, Sophia Sollberger, Paola Basilico, Thomas Kaufmann, Phillip Ian Bird, Charaf Benarafa
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:3926c7813b9048e8960603bad8c3adb42021-11-08T07:39:53ZGranule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells2296-634X10.3389/fcell.2021.630166https://doaj.org/article/3926c7813b9048e8960603bad8c3adb42021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.630166/fullhttps://doaj.org/toc/2296-634XMast cells are multifunctional immune cells scattered in tissues near blood vessels and mucosal surfaces where they mediate important reactions against parasites and contribute to the pathogenesis of allergic reactions. Serine proteases released from secretory granules upon mast cell activation contribute to these functions by modulating cytokine activity, platelet activation and proteolytic neutralization of toxins. The forced release of granule proteases into the cytosol of mast cells to induce cell suicide has recently been proposed as a therapeutic approach to reduce mast cell numbers in allergic diseases, but the molecular pathways involved in granule-mediated mast cell suicide are incompletely defined. To identify intrinsic granule proteases that can cause mast cell death, we used mice deficient in cytosolic serine protease inhibitors and their respective target proteases. We found that deficiency in Serpinb1a, Serpinb6a, and Serpinb9a or in their target proteases did not alter the kinetics of apoptosis induced by growth factor deprivation in vitro or the number of peritoneal mast cells in vivo. The serine protease cathepsin G induced marginal cell death upon mast cell granule permeabilization only when its inhibitors Serpinb1a or Serpinb6a were deleted. In contrast, the serine protease granzyme B was essential for driving apoptosis in mast cells. On granule permeabilization, granzyme B was required for caspase-3 processing and cell death. Moreover, cytosolic granzyme B inhibitor Serpinb9a prevented caspase-3 processing and mast cell death in a granzyme B-dependent manner. Together, our findings demonstrate that cytosolic serpins provide an inhibitory shield preventing granule protease-induced mast cell apoptosis, and that the granzyme B-Serpinb9a-caspase-3 axis is critical in mast cell survival and could be targeted in the context of allergic diseases.Sabrina Sofia BurgenerSabrina Sofia BurgenerMelanie BrüggerMelanie BrüggerMelanie BrüggerNathan Georges François LeborgneNathan Georges François LeborgneSophia SollbergerSophia SollbergerPaola BasilicoPaola BasilicoThomas KaufmannPhillip Ian BirdCharaf BenarafaCharaf BenarafaFrontiers Media S.A.articleserpinslysosomal peptidasescell deathgranzyme Blysosomal permeabilizationmast cellsBiology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic serpins
lysosomal peptidases
cell death
granzyme B
lysosomal permeabilization
mast cells
Biology (General)
QH301-705.5
spellingShingle serpins
lysosomal peptidases
cell death
granzyme B
lysosomal permeabilization
mast cells
Biology (General)
QH301-705.5
Sabrina Sofia Burgener
Sabrina Sofia Burgener
Melanie Brügger
Melanie Brügger
Melanie Brügger
Nathan Georges François Leborgne
Nathan Georges François Leborgne
Sophia Sollberger
Sophia Sollberger
Paola Basilico
Paola Basilico
Thomas Kaufmann
Phillip Ian Bird
Charaf Benarafa
Charaf Benarafa
Granule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells
description Mast cells are multifunctional immune cells scattered in tissues near blood vessels and mucosal surfaces where they mediate important reactions against parasites and contribute to the pathogenesis of allergic reactions. Serine proteases released from secretory granules upon mast cell activation contribute to these functions by modulating cytokine activity, platelet activation and proteolytic neutralization of toxins. The forced release of granule proteases into the cytosol of mast cells to induce cell suicide has recently been proposed as a therapeutic approach to reduce mast cell numbers in allergic diseases, but the molecular pathways involved in granule-mediated mast cell suicide are incompletely defined. To identify intrinsic granule proteases that can cause mast cell death, we used mice deficient in cytosolic serine protease inhibitors and their respective target proteases. We found that deficiency in Serpinb1a, Serpinb6a, and Serpinb9a or in their target proteases did not alter the kinetics of apoptosis induced by growth factor deprivation in vitro or the number of peritoneal mast cells in vivo. The serine protease cathepsin G induced marginal cell death upon mast cell granule permeabilization only when its inhibitors Serpinb1a or Serpinb6a were deleted. In contrast, the serine protease granzyme B was essential for driving apoptosis in mast cells. On granule permeabilization, granzyme B was required for caspase-3 processing and cell death. Moreover, cytosolic granzyme B inhibitor Serpinb9a prevented caspase-3 processing and mast cell death in a granzyme B-dependent manner. Together, our findings demonstrate that cytosolic serpins provide an inhibitory shield preventing granule protease-induced mast cell apoptosis, and that the granzyme B-Serpinb9a-caspase-3 axis is critical in mast cell survival and could be targeted in the context of allergic diseases.
format article
author Sabrina Sofia Burgener
Sabrina Sofia Burgener
Melanie Brügger
Melanie Brügger
Melanie Brügger
Nathan Georges François Leborgne
Nathan Georges François Leborgne
Sophia Sollberger
Sophia Sollberger
Paola Basilico
Paola Basilico
Thomas Kaufmann
Phillip Ian Bird
Charaf Benarafa
Charaf Benarafa
author_facet Sabrina Sofia Burgener
Sabrina Sofia Burgener
Melanie Brügger
Melanie Brügger
Melanie Brügger
Nathan Georges François Leborgne
Nathan Georges François Leborgne
Sophia Sollberger
Sophia Sollberger
Paola Basilico
Paola Basilico
Thomas Kaufmann
Phillip Ian Bird
Charaf Benarafa
Charaf Benarafa
author_sort Sabrina Sofia Burgener
title Granule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells
title_short Granule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells
title_full Granule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells
title_fullStr Granule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells
title_full_unstemmed Granule Leakage Induces Cell-Intrinsic, Granzyme B-Mediated Apoptosis in Mast Cells
title_sort granule leakage induces cell-intrinsic, granzyme b-mediated apoptosis in mast cells
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/3926c7813b9048e8960603bad8c3adb4
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