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dc.contributor.authorTrujillo Vargas, Claudia Milena-
dc.contributor.authorGalletti, Jeremias G.-
dc.contributor.authorScholand, Kaitlin K.-
dc.contributor.authorHaap, Wolfgang-
dc.contributor.authorSantos Ferreira, Tiago-
dc.contributor.authorUllmer, Christoph-
dc.contributor.authorYu, Zhiyuan-
dc.contributor.authorde Paiva, Cintia S.-
dc.date.accessioned2024-04-17T15:36:23Z-
dc.date.available2024-04-17T15:36:23Z-
dc.date.issued2023-
dc.identifier.citationGalletti JG, Scholand KK, Trujillo-Vargas CM, Haap W, Santos-Ferreira T, Ullmer C, Yu Z, de Paiva CS. Effects of Cathepsin S Inhibition in the Age-Related Dry Eye Phenotype. Invest Ophthalmol Vis Sci. 2023 Aug 1;64(11):7. doi: 10.1167/iovs.64.11.7. Erratum in: Invest Ophthalmol Vis Sci. 2023 Aug 1;64(11):32.spa
dc.identifier.issn0146-0404-
dc.identifier.urihttps://hdl.handle.net/10495/39048-
dc.description.abstractABSTRACT: Purpose: Aged C57BL/6J (B6) mice have increased levels of cathepsin S, and aged cathepsin S (Ctss-/-) knockout mice are resistant to age-related dry eye. This study investigated the effects of cathepsin S inhibition on age-related dry eye disease. Methods: Female B6 mice aged 15.5 to 17 months were randomized to receive a medicated diet formulated by mixing the RO5461111 cathepsin S inhibitor or a standard diet for at least 12 weeks. Cornea mechanosensitivity was measured with a Cochet-Bonnet esthesiometer. Ocular draining lymph nodes and lacrimal glands (LGs) were excised and prepared for histology or assayed by flow cytometry to quantify infiltrating immune cells. The inflammatory foci (>50 cells) were counted under a 10× microscope lens and quantified using the focus score. Goblet cell density was investigated in periodic acid-Schiff stained sections. Ctss-/- mice were compared to age-matched wild-type mice. Results: Aged mice subjected to cathepsin S inhibition or Ctss-/- mice showed improved conjunctival goblet cell density and cornea mechanosensitivity. There was no change in total LG focus score in the diet or Ctss-/- mice, but there was a lower frequency of CD4+IFN-γ+ cell infiltration in the LGs. Furthermore, aged Ctss-/- LGs had an increase in T central memory, higher numbers of CD19+B220-, and fewer CD19+B220+ cells than wild-type LGs. Conclusions: Our results indicate that therapies aimed at decreasing cathepsin S can ameliorate age-related dry eye disease with a highly beneficial impact on the ocular surface. Further studies are needed to investigate the role of cathepsin S during aging.spa
dc.format.extent12 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherAssociation for Research in Vision and Ophthalmologyspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleEffects of Cathepsin S Inhibition in the Age-Related Dry Eye Phenotypespa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupInmunodeficiencias Primariasspa
dc.identifier.doi10.1167/iovs.64.11.7-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1552-5783-
oaire.citationtitleInvestigative Ophthalmology and Visual Sciencespa
oaire.citationstartpage1spa
oaire.citationendpage12spa
oaire.citationvolume64spa
oaire.citationissue11spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
dc.publisher.placeSan Luis, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsModelos Animales de Enfermedad-
dc.subject.decsDisease Models, Animal-
dc.subject.decsSíndromes de Ojo Seco-
dc.subject.decsDry Eye Syndromes-
dc.subject.decsEnfermedades del Aparato Lagrimal-
dc.subject.decsLacrimal Apparatus Diseases-
dc.subject.decsRatones Endogámicos C57BL-
dc.subject.decsMice, Inbred C57BL-
dc.subject.decsAlcohol Polivinílico-
dc.subject.decsPolyvinyl Alcohol-
dc.subject.decsLagrimas - metabolismo-
dc.subject.decsTears - metabolism-
dc.description.researchgroupidCOL0012426spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D015352-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D008810-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D004195-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D007766-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D011142-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D013666-
dc.relation.ispartofjournalabbrevInvest. Ophthalmol. Vis. Sci.spa
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