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A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium
Members of the Rab guanosine triphosphatase (GTPase) family are key regulators of membrane traffic. Here we examined the association of 48 Rabs with model phagosomes containing a non-invasive mutant of Salmonella enterica serovar Typhimurium (S. Typhimurium). This mutant traffics to lysosomes and al...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063952/ https://www.ncbi.nlm.nih.gov/pubmed/17261845 http://dx.doi.org/10.1083/jcb.200611056 |
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author | Smith, Adam C. Heo, Won Do Braun, Virginie Jiang, Xiuju Macrae, Chloe Casanova, James E. Scidmore, Marci A. Grinstein, Sergio Meyer, Tobias Brumell, John H. |
author_facet | Smith, Adam C. Heo, Won Do Braun, Virginie Jiang, Xiuju Macrae, Chloe Casanova, James E. Scidmore, Marci A. Grinstein, Sergio Meyer, Tobias Brumell, John H. |
author_sort | Smith, Adam C. |
collection | PubMed |
description | Members of the Rab guanosine triphosphatase (GTPase) family are key regulators of membrane traffic. Here we examined the association of 48 Rabs with model phagosomes containing a non-invasive mutant of Salmonella enterica serovar Typhimurium (S. Typhimurium). This mutant traffics to lysosomes and allowed us to determine which Rabs localize to a maturing phagosome. In total, 18 Rabs associated with maturing phagosomes, each with its own kinetics of association. Dominant-negative mutants of Rab23 and 35 inhibited phagosome–lysosome fusion. A large number of Rab GTPases localized to wild-type Salmonella-containing vacuoles (SCVs), which do not fuse with lysosomes. However, some Rabs (8B, 13, 23, 32, and 35) were excluded from wild-type SCVs whereas others (5A, 5B, 5C, 7A, 11A, and 11B) were enriched on this compartment. Our studies demonstrate that a complex network of Rab GTPases controls endocytic progression to lysosomes and that this is modulated by S. Typhimurium to allow its intracellular growth. |
format | Text |
id | pubmed-2063952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20639522007-11-29 A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium Smith, Adam C. Heo, Won Do Braun, Virginie Jiang, Xiuju Macrae, Chloe Casanova, James E. Scidmore, Marci A. Grinstein, Sergio Meyer, Tobias Brumell, John H. J Cell Biol Research Articles Members of the Rab guanosine triphosphatase (GTPase) family are key regulators of membrane traffic. Here we examined the association of 48 Rabs with model phagosomes containing a non-invasive mutant of Salmonella enterica serovar Typhimurium (S. Typhimurium). This mutant traffics to lysosomes and allowed us to determine which Rabs localize to a maturing phagosome. In total, 18 Rabs associated with maturing phagosomes, each with its own kinetics of association. Dominant-negative mutants of Rab23 and 35 inhibited phagosome–lysosome fusion. A large number of Rab GTPases localized to wild-type Salmonella-containing vacuoles (SCVs), which do not fuse with lysosomes. However, some Rabs (8B, 13, 23, 32, and 35) were excluded from wild-type SCVs whereas others (5A, 5B, 5C, 7A, 11A, and 11B) were enriched on this compartment. Our studies demonstrate that a complex network of Rab GTPases controls endocytic progression to lysosomes and that this is modulated by S. Typhimurium to allow its intracellular growth. The Rockefeller University Press 2007-01-29 /pmc/articles/PMC2063952/ /pubmed/17261845 http://dx.doi.org/10.1083/jcb.200611056 Text en Copyright © 2007, The Rockefeller University Press 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 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Smith, Adam C. Heo, Won Do Braun, Virginie Jiang, Xiuju Macrae, Chloe Casanova, James E. Scidmore, Marci A. Grinstein, Sergio Meyer, Tobias Brumell, John H. A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium |
title | A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium |
title_full | A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium |
title_fullStr | A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium |
title_full_unstemmed | A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium |
title_short | A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium |
title_sort | network of rab gtpases controls phagosome maturation and is modulated by salmonella enterica serovar typhimurium |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063952/ https://www.ncbi.nlm.nih.gov/pubmed/17261845 http://dx.doi.org/10.1083/jcb.200611056 |
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