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Physiological and pathophysiological functions of NLRP6: pro- and anti-inflammatory roles

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dc.contributor.author Angosto-Bazarra, Diego
dc.contributor.author Molina-López, Cristina
dc.contributor.author Pelegrín, Pablo
dc.date.accessioned 2025-11-19T15:37:38Z
dc.date.available 2025-11-19T15:37:38Z
dc.date.issued 2022-06
dc.identifier.citation Angosto-Bazarra D, Molina-López C, Pelegrín P. Physiological and pathophysiological functions of NLRP6: pro- and anti-inflammatory roles. Commun Biol. 1 de junio de 2022;5(1):524.
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21338
dc.description.abstract The nucleotide-binding oligomerization and leucine-rich repeat receptor (NLR) protein family consists of important immune sensors that form inflammasomes, a cytosolic multi-protein platform that induces caspase-1 activation and is involved in different inflammatory pathologies. The NLR family pyrin domain containing 6 (NLRP6) is a receptor that can signal by forming inflammasomes, but which can also play an important role without forming inflammasomes. NLRP6 regulates intestinal homeostasis and inflammation, but also is involved in cancer, the nervous system or liver diseases, with both protective and deleterious consequences. In the present article, we review the different roles of NLRP6 in these processes and offer new insights into NLRP6 activation.
dc.language.iso eng
dc.publisher NATURE PORTFOLIO
dc.rights Atribución-NoComercial-SinDerivadas 3.0 España
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/es *
dc.subject.mesh Anti-Inflammatory Agents/pharmacology
dc.subject.mesh Carrier Proteins
dc.subject.mesh Humans
dc.subject.mesh Inflammasomes/metabolism
dc.subject.mesh Inflammation/pathology
dc.subject.mesh Intestines
dc.subject.mesh Intracellular Signaling Peptides and Proteins/metabolism
dc.title Physiological and pathophysiological functions of NLRP6: pro- and anti-inflammatory roles
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 35650327
dc.relation.publisherversion https://www.nature.com/articles/s42003-022-03491-w
dc.identifier.doi 10.1038/s42003-022-03491-w
dc.journal.title Communications Biology
dc.identifier.essn 2399-3642


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