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dc.contributor.authorNavarro, María N.-
dc.contributor.authorGómez de las Heras, Manuel M.-
dc.contributor.authorMittelbrunn, María-
dc.date.accessioned2022-04-25T10:00:03Z-
dc.date.available2022-04-25T10:00:03Z-
dc.date.issued2021-03-26-
dc.identifierdoi: 10.1111/bph.15477-
dc.identifierissn: 1476-5381-
dc.identifier.citationBritish Journal of Pharmacology (2021)-
dc.identifier.urihttp://hdl.handle.net/10261/267736-
dc.description.abstractMetabolism is dynamically regulated to accompany immune cell function, and altered immunometabolism can result in impaired immune responses. Concomitantly, the pharmacological manipulation of metabolic processes offers an opportunity for therapeutic intervention in inflammatory disorders. The nicotinamide adenine dinucleotide (NAD+) is a critical metabolic intermediate that serves as enzyme cofactor in redox reactions, and is also used as a co-substrate by many enzymes such as sirtuins, adenosine diphosphate ribose transferases and synthases. Through these activities, NAD+ metabolism regulates a broad spectrum of cellular functions such as energy metabolism, DNA repair, regulation of the epigenetic landscape and inflammation. Thus, the manipulation of NAD+ availability using pharmacological compounds such as NAD+ precursors can have immune-modulatory properties in inflammation. Here, we discuss how the NAD+ metabolism contributes to the immune response and inflammatory conditions, with a special focus on multiple sclerosis, inflammatory bowel diseases and inflammageing-
dc.description.sponsorshipSpanish Ministry of Science and Innovation (PID2019-110511RB-I00) to M.N.N, and the H2020-EU.1.1, European Research Council (ERC-2016-StG 715322-EndoMitTalk), Fondo de Investigación Sanitaria del Instituto de Salud Carlos III (PI19/855) to M.M, Fondo Europeo de Desarrollo Regional (FEDER) to M.M and M.N.N. M.M.GH was funded by the Spanish Ministry of Science, Innovation and Universities (FPU19/02576). M.M. is supported by the Miguel Servet program (CPII19/00014, Fundación de Investigación del Hospital 12 de Octubre). Institutional grants from the Fundación Ramón Areces and Banco de Santander to the CBMSO are also acknowledged.-
dc.languageeng-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.subjectAgeing-
dc.subjectCD38-
dc.subjectExperimental autoimmune encephalomyelitis-
dc.subjectInflammation-
dc.subjectlymphocytes-
dc.subjectNAD+-
dc.subjectT Cells-
dc.titleNicotinamide adenine dinucleotide metabolism in the immune response, autoimmunity and inflammageing-
dc.typeartículo-
dc.identifier.doi10.1111/bph.15477-
dc.relation.publisherversionhttp://dx.doi.org/10.1111/bph.15477-
dc.date.updated2022-04-25T10:00:03Z-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.contributor.funderEuropean Research Council-
dc.contributor.funderInstituto de Salud Carlos III-
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)-
dc.contributor.funderInstituto de Investigación Hospital 12 de Octubre-
dc.contributor.funderFundación Ramón Areces-
dc.contributor.funderBanco Santander-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000781es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100008054es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100010784es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004587es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeartículo-
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