Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/42160
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dc.contributor.authorA-Gonzalez, Noeliaen_US
dc.contributor.authorCastrillo, Antonioen_US
dc.date.accessioned2018-10-17T11:06:48Z-
dc.date.available2018-10-17T11:06:48Z-
dc.date.issued2018en_US
dc.identifier.issn0008-8749en_US
dc.identifier.urihttp://hdl.handle.net/10553/42160-
dc.description.abstractMacrophage heterogeneity in the spleen has been long documented, with four subsets populating the different splenic compartments. The diverse environments on the splenic compartments determine their varied phenotype and functions. In the white pulp, highly phagocytic macrophages contribute to the generation of the immune response. The marginal zone contains two populations of macrophages, which also contribute to the immune response. Their strategic position in the bloodstream and their unique phenotype confer them a crucial role in the defense against blood borne pathogens, placing them at the crossroad between innate and adaptive immune responses. Macrophages in the red pulp are classically linked to homeostatic and metabolic functions in erythrocyte phagocytosis and iron recycling. We review here recent advances demonstrating the importance of macrophage ontogeny and organ development in determining the phenotype, transcriptional profile and, ultimately, the functions of the populations of splenic macrophages.en_US
dc.languageengen_US
dc.publisher0008-8749
dc.relation.ispartofCellular immunology (Print)en_US
dc.sourceCellular Immunology [ISSN 0008-8749], v. 330, p. 151-158en_US
dc.subject32 Ciencias médicasen_US
dc.subject.otherMacrophagesen_US
dc.subject.otherSpleenen_US
dc.subject.otherTranscriptional regulationen_US
dc.subject.otherTissue microenvironmenten_US
dc.titleOrigin and specialization of splenic macrophagesen_US
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1016/j.cellimm.2018.05.005
dc.identifier.scopus85047115409
dc.identifier.isi000441889600019
dc.contributor.authorscopusid28567533000
dc.contributor.authorscopusid55445301000
dc.description.lastpage158-
dc.description.firstpage151-
dc.relation.volume330-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid34354606
dc.contributor.daisngid225640
dc.contributor.wosstandardWOS:A-Gonzalez, N
dc.contributor.wosstandardWOS:Castrillo, A
dc.date.coverdateAgosto 2018
dc.identifier.ulpgces
dc.description.sjr1,275
dc.description.jcr3,291
dc.description.sjrqQ2
dc.description.jcrqQ2
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0002-2057-2159-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameCastrillo Viguera, Antonio Jesús-
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