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dc.contributor.authorMartínez-Fábregas, Jonathanes_ES
dc.contributor.authorTamargo-Azpilicueta, Joaquines_ES
dc.contributor.authorDíaz-Moreno, Irenees_ES
dc.date.accessioned2022-03-30T12:54:50Z-
dc.date.available2022-03-30T12:54:50Z-
dc.date.issued2022-
dc.identifier.citationFEBS Open Bio (2022)es_ES
dc.identifier.issn2211-5463-
dc.identifier.urihttp://hdl.handle.net/10261/265788-
dc.description17 p.es_ES
dc.description.abstractMore than 50 years have passed since Nobel laureate Cristian de Duve described for the first time the presence of tiny subcellular compartments filled with hydrolytic enzymes: the lysosome. For a long time, lysosomes were deemed simple waste bags exerting a plethora of hydrolytic activities involved in the recycling of biopolymers, and lysosomal genes were considered to just be simple housekeeping genes, transcribed in a constitutive fashion. However, lysosomes are emerging as multifunctional signalling hubs involved in multiple aspects of cell biology, both under homeostatic and pathological conditions. Lysosomes are involved in the regulation of cell metabolism through the mTOR/TFEB axis. They are also key players in the regulation and onset of the immune response. Furthermore, it is becoming clear that lysosomal hydrolases can regulate several biological processes outside of the lysosome. They are also implicated in a complex communication network among subcellular compartments that involves intimate organelle-to-organelle contacts. Furthermore, lysosomal dysfunction is nowadays accepted as the causative event behind several human pathologies: low frequency inherited diseases, cancer, or neurodegenerative, metabolic, inflammatory, and autoimmune diseases. Recent advances in our knowledge of the complex biology of lysosomes have established them as promising therapeutic targets for the treatment of different pathologies. Although recent discoveries have started to highlight that lysosomes are controlled by a complex web of regulatory networks, which in some cases seem to be cell- and stimuli-dependent, to harness the full potential of lysosomes as therapeutic targets, we need a deeper understanding of the little-known signalling pathways regulating this subcellular compartment and its functions.es_ES
dc.description.sponsorshipThis work was supported by “Project PGC2018-096049-B-I00, financiado por: FEDER/Ministerio de Ciencia eI Innovación—Agencia Estatal de Investigación”. This work was also supported by the Regional Government of Andalusia (BIO198, US-1254317 US/JUNTA/FEDER, UE, US-1257019 US/JUNTA/FEDER/UE, P18-FR-3487 and P18-HO-5091) and the Ramón Areces Foundation (2021-2023). JMF is supported by an EU Marie Skłodowska Curie Action (MSCA) Individual Fellowship (CytoLysoReg101025429). We extend our thanks to Dr. Reyes Sanles Falagan for critical reading of the manuscript.es_ES
dc.language.isoenges_ES
dc.publisherJohn Wiley & Sonses_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-096049-B-I00/ES/APROXIMACIONES ESTRUCTURALES Y FUNCIONALES A LOS MECANISMOS MOLECULARES DEPENDIENTES DE CITOCROMO C QUE REGULAN LA ACTIVIDAD DE LAS CHAPERONAS DE HISTONAS BAJO DAÑO EN EL ADN/es_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.subjectLysosomeses_ES
dc.subjectmTORC1es_ES
dc.subjectsignalling pathwayses_ES
dc.subjectSTATses_ES
dc.subjectTFEBes_ES
dc.subjecttranscriptional regulationes_ES
dc.titleLysosomes: multifunctional compartments ruled by a complex regulatory networkes_ES
dc.typeartículo de revisiónes_ES
dc.identifier.doi10.1002/2211-5463.13387-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1002/2211-5463.13387es_ES
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/es_ES
dc.contributor.funderMinisterio de Ciencia e Innovación (España)es_ES
dc.contributor.funderJunta de Andalucíaes_ES
dc.contributor.funderFundación Ramón Areceses_ES
dc.contributor.funderEuropean Commissiones_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100008054es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011011es_ES
dc.contributor.orcidMartínez-Fábregas, Jonathan [0000-0001-5809-065X]es_ES
dc.contributor.orcidTamargo-Azpilicueta, Joaquín [0000-0001-8504-4472]es_ES
dc.contributor.orcidDíaz-Moreno, Irene [0000-0002-5318-7644]es_ES
dc.identifier.pmid35218162-
dc.identifier.scopus2-s2.0-85125931226-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85125931226-
dc.type.coarhttp://purl.org/coar/resource_type/c_dcae04bces_ES
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypeartículo de revisión-
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