Please use this identifier to cite or link to this item: https://doi.org/10.1038/nm.2036
DC FieldValue
dc.titleSalmonella disrupts lymph node architecture by TLR4-mediated suppression of homeostatic chemokines
dc.contributor.authorSt John, A.L.
dc.contributor.authorAbraham, S.N.
dc.date.accessioned2016-11-11T07:59:59Z
dc.date.available2016-11-11T07:59:59Z
dc.date.issued2009-11
dc.identifier.citationSt John, A.L., Abraham, S.N. (2009-11). Salmonella disrupts lymph node architecture by TLR4-mediated suppression of homeostatic chemokines. Nature Medicine 15 (11) : 1259-1265. ScholarBank@NUS Repository. https://doi.org/10.1038/nm.2036
dc.identifier.issn10788956
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/130016
dc.description.abstractWe report that infection of draining lymph nodes (DLNs) by Salmonella typhimurium results in the specific downregulation of the homeostatic chemokines CCL21 and CXCL13, which are essential for normal DLN organization and function. Our data reveal that the mechanism of this suppression is dependent on S. typhimurium LPS (sLPS). The decrease in CCL21 expression involves interaction between sLPS and CCL21-producing cells within DLNs, triggering a distinct Toll-like receptor 4 (TLR4)-mediated host signaling response. In this response, suppressor of cytokine signaling-3 (Socs3) is upregulated, which negatively regulates mothers against decapentaplegic homolog-3 (Smad3)-initiated production of CCL21. Disruption of lymph node architecture and cellular trafficking enhances S. typhimurium virulence and could represent a mechanism of immune suppression used by pathogens that primarily target lymphoid tissue. © 2009 Nature America, Inc. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1038/nm.2036
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentDUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
dc.description.doi10.1038/nm.2036
dc.description.sourcetitleNature Medicine
dc.description.volume15
dc.description.issue11
dc.description.page1259-1265
dc.description.codenNAMEF
dc.identifier.isiut000271543700013
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