CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis

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dc.contributor.authorSantos, Isako
dc.contributor.authorColaco, Henrique G.ko
dc.contributor.authorNeves-Costaa, Anako
dc.contributor.authorSeixas, Elsako
dc.contributor.authorVelho, Tiago R.ko
dc.contributor.authorPedroso, Dorako
dc.contributor.authorBarros, Andreko
dc.contributor.authorMartins, Ruiko
dc.contributor.authorCarvalho, Nunoko
dc.contributor.authorPayen, Didierko
dc.contributor.authorWeis, Sebastianko
dc.contributor.authorYi, Hyon-Seungko
dc.contributor.authorShong, Minhoko
dc.contributor.authorMoita, Luis F.ko
dc.date.accessioned2023-04-14T01:00:52Z-
dc.date.available2023-04-14T01:00:52Z-
dc.date.created2023-04-14-
dc.date.created2023-04-14-
dc.date.issued2020-06-
dc.identifier.citationPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, v.117, no.22, pp.12281 - 12287-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10203/306236-
dc.description.abstractSepsis is a life-threatening organ dysfunction condition caused by a dysregulated host response to an infection. Here we report that the circulating levels of growth and differentiation factor-15 (GDF15) are strongly increased in septic shock patients and correlate with mortality. In mice, we find that peptidoglycan is a potent ligand that signals through the TLR2-Myd88 axis for the secretion of GDF15, and that Gdf15-deficient mice are protected against abdominal sepsis due to increased chemokine CXC ligand 5 (CXCL5)-mediated recruitment of neutrophils into the peritoneum, leading to better local bacterial control. Our results identify GDF15 as a potential target to improve sepsis treatment. Its inhibition should increase neutrophil recruitment to the site of infection and consequently lead to better pathogen control and clearance.-
dc.languageEnglish-
dc.publisherNATL ACAD SCIENCES-
dc.titleCXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis-
dc.typeArticle-
dc.identifier.wosid000538147800057-
dc.type.rimsART-
dc.citation.volume117-
dc.citation.issue22-
dc.citation.beginningpage12281-
dc.citation.endingpage12287-
dc.citation.publicationnamePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-
dc.identifier.doi10.1073/pnas.1918508117/-/DCSupplemental-
dc.contributor.localauthorShong, Minho-
dc.contributor.nonIdAuthorSantos, Isa-
dc.contributor.nonIdAuthorColaco, Henrique G.-
dc.contributor.nonIdAuthorNeves-Costaa, Ana-
dc.contributor.nonIdAuthorSeixas, Elsa-
dc.contributor.nonIdAuthorVelho, Tiago R.-
dc.contributor.nonIdAuthorPedroso, Dora-
dc.contributor.nonIdAuthorBarros, Andre-
dc.contributor.nonIdAuthorMartins, Rui-
dc.contributor.nonIdAuthorCarvalho, Nuno-
dc.contributor.nonIdAuthorPayen, Didier-
dc.contributor.nonIdAuthorWeis, Sebastian-
dc.contributor.nonIdAuthorYi, Hyon-Seung-
dc.contributor.nonIdAuthorMoita, Luis F.-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorsepsis-
dc.subject.keywordAuthorGDF15-
dc.subject.keywordAuthorneutrophils-
dc.subject.keywordAuthorCXCL5-
dc.subject.keywordPlusINTEGRIN ACTIVATION-
dc.subject.keywordPlusWEIGHT-LOSS-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusGDF15-
dc.subject.keywordPlusGDF-15-
dc.subject.keywordPlusTOLERANCE-
dc.subject.keywordPlusOBESITY-
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