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dc.contributor.authorBullón, Pedro-
dc.contributor.authorCastejón-Vega, Beatriz-
dc.contributor.authorRomán-Malo, Lourdes-
dc.contributor.authorJiménez-Guerrero, Maripaz-
dc.contributor.authorCotán, David-
dc.contributor.authorForbes-Hernandez, Tamara Y.-
dc.contributor.authorVarela‐López, Alfonso-
dc.contributor.authorPérez-Pulido, Antonio J.-
dc.contributor.authorGiampieri, Francesca-
dc.contributor.authorQuiles, José Luis-
dc.contributor.authorBattino, Maurizio-
dc.contributor.authorSánchez-Alcázar, José Antonio-
dc.contributor.authorCordero, Mario D.-
dc.date.accessioned2021-06-01T13:00:12Z-
dc.date.available2021-06-01T13:00:12Z-
dc.date.issued2018-
dc.identifier.citationJournal of Allergy and Clinical Immunology 142(4): 1131-1143.e7 (2018)-
dc.identifier.issn0091-6749-
dc.identifier.urihttp://hdl.handle.net/10261/242247-
dc.description.abstract[Background]: Cathepsin C (CatC) is a lysosomal enzyme involved in activation of serine proteases from immune and inflammatory cells. Several loss-of-function mutations in the CatC gene have been shown to be the genetic mark of Papillon-Lefèvre syndrome (PLS), a rare autosomal recessive disease characterized by severe early-onset periodontitis, palmoplantar hyperkeratosis, and increased susceptibility to infections. Deficiencies or dysfunction in other cathepsin family proteins, such as cathepsin B or D, have been associated with autophagic and lysosomal disorders.-
dc.description.abstract[Objectives]: Here we characterized the basis for autophagic dysfunction in patients with PLS by analyzing skin fibroblasts derived from patients with several mutations in the CatC gene and reduced enzymatic activity.-
dc.description.abstract[Methods]: Skin fibroblasts were isolated from patients with PLS assessed by using genetic analysis. Authophagic flux dysfunction was evaluated by examining accumulation of p62/SQSTM1 and a bafilomycin assay. Ultrastructural analysis further confirmed abnormal accumulation of autophagic vesicles in mutant cells. A recombinant CatC protein was produced by a baculovirus system in insect cell cultures.-
dc.description.abstract[Results]: Mutant fibroblasts from patients with PLS showed alterations in oxidative/antioxidative status, reduced oxygen consumption, and a marked autophagic dysfunction associated with autophagosome accumulation. These alterations were accompanied by lysosomal permeabilization, cathepsin B release, and NLR family pyrin domain containing 3 (NLRP3) inflammasome activation. Treatment of mutant fibroblasts with recombinant CatC improved cell growth and autophagic flux and partially restored lysosomal permeabilization.-
dc.description.abstract[Conclusions]: Our data provide a novel molecular mechanism underlying PLS. Impaired autophagy caused by insufficient lysosomal function might represent a new therapeutic target for PLS.-
dc.languageeng-
dc.publisherElsevier-
dc.rightsclosedAccess-
dc.subjectPapillon-Lefèvre syndrome-
dc.subjectCathepsin C-
dc.subjectAutophagy-
dc.subjectLysosomal permeabilization-
dc.titleAutophagic dysfunction in Papillon Lefèvre syndrome is restored by recombinant Cathepsin C treatment-
dc.typeartículo-
dc.identifier.doihttp://dx.doi.org/10.1016/j.jaci.2018.01.018-
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.jaci.2018.01.018-
dc.date.updated2021-06-01T13:00:13Z-
dc.relation.csic-
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