A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium

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dc.contributor.authorSmith, Adam C.ko
dc.contributor.authorHeo, Won Doko
dc.contributor.authorBraun, Virginieko
dc.contributor.authorJiang, Xiujuko
dc.contributor.authorMacrae, Chloeko
dc.contributor.authorCasanova, James E.ko
dc.contributor.authorScidmore, Marci A.ko
dc.contributor.authorGrinstein, Sergioko
dc.contributor.authorMeyer, Tobiasko
dc.contributor.authorBrumell, John H.ko
dc.date.accessioned2013-03-07T01:18:11Z-
dc.date.available2013-03-07T01:18:11Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2007-01-
dc.identifier.citationJOURNAL OF CELL BIOLOGY, v.176, no.3, pp.263 - 268-
dc.identifier.issn0021-9525-
dc.identifier.urihttp://hdl.handle.net/10203/89054-
dc.description.abstractMembers 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.-
dc.languageEnglish-
dc.publisherROCKEFELLER UNIV PRESS-
dc.titleA network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium-
dc.typeArticle-
dc.identifier.wosid000243997700003-
dc.identifier.scopusid2-s2.0-33846576162-
dc.type.rimsART-
dc.citation.volume176-
dc.citation.issue3-
dc.citation.beginningpage263-
dc.citation.endingpage268-
dc.citation.publicationnameJOURNAL OF CELL BIOLOGY-
dc.identifier.doi10.1083/jcb.200611056-
dc.contributor.localauthorHeo, Won Do-
dc.contributor.nonIdAuthorSmith, Adam C.-
dc.contributor.nonIdAuthorBraun, Virginie-
dc.contributor.nonIdAuthorJiang, Xiuju-
dc.contributor.nonIdAuthorMacrae, Chloe-
dc.contributor.nonIdAuthorCasanova, James E.-
dc.contributor.nonIdAuthorScidmore, Marci A.-
dc.contributor.nonIdAuthorGrinstein, Sergio-
dc.contributor.nonIdAuthorMeyer, Tobias-
dc.contributor.nonIdAuthorBrumell, John H.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusTRANS-GOLGI NETWORK-
dc.subject.keywordPlusCONTAINING VACUOLES-
dc.subject.keywordPlusEPITHELIAL-CELLS-
dc.subject.keywordPlusLATE ENDOSOMES-
dc.subject.keywordPlusENDOCYTIC PATHWAY-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusMACROPHAGES-
dc.subject.keywordPlusLYSOSOMES-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusBIOGENESIS-
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