Cargando…
Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions
Antigen processing and presentation and cytotoxic targeting depend on the activities of several lysosomal enzymes that require mannose 6-phosphate (M6P) sorting signals for efficient intracellular transport and localization. In this paper, we show that mice deficient in the formation of M6P residues...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298682/ https://www.ncbi.nlm.nih.gov/pubmed/25601403 http://dx.doi.org/10.1083/jcb.201407077 |
_version_ | 1782353278874419200 |
---|---|
author | Otomo, Takanobu Schweizer, Michaela Kollmann, Katrin Schumacher, Valéa Muschol, Nicole Tolosa, Eva Mittrücker, Hans-Willi Braulke, Thomas |
author_facet | Otomo, Takanobu Schweizer, Michaela Kollmann, Katrin Schumacher, Valéa Muschol, Nicole Tolosa, Eva Mittrücker, Hans-Willi Braulke, Thomas |
author_sort | Otomo, Takanobu |
collection | PubMed |
description | Antigen processing and presentation and cytotoxic targeting depend on the activities of several lysosomal enzymes that require mannose 6-phosphate (M6P) sorting signals for efficient intracellular transport and localization. In this paper, we show that mice deficient in the formation of M6P residues exhibit significant loss of cathepsin proteases in B cells, leading to lysosomal dysfunction with accumulation of storage material, impaired antigen processing and presentation, and subsequent defects in B cell maturation and antibody production. The targeting of lysosomal and granular enzymes lacking M6P residues is less affected in dendritic cells and T cells and sufficient for maintenance of degradative and lytic functions. M6P deficiency also impairs serum immunoglobulin levels and antibody responses to vaccination in patients. Our data demonstrate the critical role of M6P-dependent transport routes for B cell functions in vivo and humoral immunity in mice and human. |
format | Online Article Text |
id | pubmed-4298682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42986822015-07-19 Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions Otomo, Takanobu Schweizer, Michaela Kollmann, Katrin Schumacher, Valéa Muschol, Nicole Tolosa, Eva Mittrücker, Hans-Willi Braulke, Thomas J Cell Biol Research Articles Antigen processing and presentation and cytotoxic targeting depend on the activities of several lysosomal enzymes that require mannose 6-phosphate (M6P) sorting signals for efficient intracellular transport and localization. In this paper, we show that mice deficient in the formation of M6P residues exhibit significant loss of cathepsin proteases in B cells, leading to lysosomal dysfunction with accumulation of storage material, impaired antigen processing and presentation, and subsequent defects in B cell maturation and antibody production. The targeting of lysosomal and granular enzymes lacking M6P residues is less affected in dendritic cells and T cells and sufficient for maintenance of degradative and lytic functions. M6P deficiency also impairs serum immunoglobulin levels and antibody responses to vaccination in patients. Our data demonstrate the critical role of M6P-dependent transport routes for B cell functions in vivo and humoral immunity in mice and human. The Rockefeller University Press 2015-01-19 /pmc/articles/PMC4298682/ /pubmed/25601403 http://dx.doi.org/10.1083/jcb.201407077 Text en © 2015 Otomo 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 Otomo, Takanobu Schweizer, Michaela Kollmann, Katrin Schumacher, Valéa Muschol, Nicole Tolosa, Eva Mittrücker, Hans-Willi Braulke, Thomas Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions |
title | Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions |
title_full | Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions |
title_fullStr | Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions |
title_full_unstemmed | Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions |
title_short | Mannose 6 phosphorylation of lysosomal enzymes controls B cell functions |
title_sort | mannose 6 phosphorylation of lysosomal enzymes controls b cell functions |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298682/ https://www.ncbi.nlm.nih.gov/pubmed/25601403 http://dx.doi.org/10.1083/jcb.201407077 |
work_keys_str_mv | AT otomotakanobu mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions AT schweizermichaela mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions AT kollmannkatrin mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions AT schumachervalea mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions AT muscholnicole mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions AT tolosaeva mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions AT mittruckerhanswilli mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions AT braulkethomas mannose6phosphorylationoflysosomalenzymescontrolsbcellfunctions |