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dc.contributor.authorOspina Gómez, Juan Pablo-
dc.contributor.authorCardona Castro, Nora-
dc.contributor.authorSerrano Coll, Héctor-
dc.contributor.authorSalazar Peláez, Lina-
dc.date.accessioned2024-11-03T14:22:46Z-
dc.date.available2024-11-03T14:22:46Z-
dc.date.issued2020-
dc.identifier.citationSerrano-Coll H, Ospina JP, Salazar-Peláez L, Cardona-Castro N. Notch Signaling Pathway Expression in the Skin of Leprosy Patients: Association With Skin and Neural Damage. Front Immunol. 2020 Mar 19;11:368. doi: 10.3389/fimmu.2020.00368.spa
dc.identifier.urihttps://hdl.handle.net/10495/43090-
dc.description.abstractABSTRACT: Leprosy is an infectious disease caused by Mycobacterium leprae, a debilitating disease that affects the skin and peripheral nerves. It is possible that tissue changes during infection with leprosy are related to alterations in the activity of the Notch signaling pathway, an innate signaling pathway in the physiology of the skin and peripheral nerves. Methods: This is a descriptive observational study. Thirty skin biopsies from leprosy patients and 15 from individuals with no history of this disease were evaluated. In these samples, gene expressions of cellular components associated with the Notch signaling pathway, Hes-1, Hey-1, Runx-1 Jagged-1, Notch-1, and Numb, were evaluated using q-PCR, and protein expression was evaluated using immunohistochemistry of Runx-1 and Hes-1. Results: Changes were observed in the transcription of Notch signaling pathway components; Hes-1 was downregulated and Runx-1 upregulated in the skin of infected patients. These results were confirmed by immunohistochemistry, where reduction of Hes-1 expression was found in the epidermis, eccrine glands, and hair follicles. Increased expression of Runx-1 was found in inflammatory cells in the dermis of infected patients; however, it is not related to tissue changes. With these results, a multivariate analysis was performed to determine the causes of transcription factor Hes-1 reduction. It was concluded that tissue inflammation was the main cause. Conclusions: The tissue changes found in the skin of infected patients could be associated with a reduction in the expression of Hes-1, a situation that would promote the survival and proliferation of M. leprae in this tissue.spa
dc.format.extent17 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherFrontiers Research Foundationspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleNotch Signaling Pathway Expression in the Skin of Leprosy Patients: Association With Skin and Neural Damagespa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupCentro de de Investigaciones Dermatológicasspa
dc.identifier.doi10.3389/fimmu.2020.00368-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1664-3224-
oaire.citationtitleFrontiers in Immunologyspa
oaire.citationstartpage1spa
oaire.citationendpage17spa
oaire.citationvolume11spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
oaire.fundernameColombia. Ministerio de Ciencia, Tecnología e Innovación - MinCienciasspa
dc.publisher.placeLausana, Suizaspa
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.decsCore Binding Factor Alpha 2 Subunit-
dc.subject.decsSubunidad alfa 2 del Factor de Unión al Sitio Principal-
dc.subject.decsCyclin D1-
dc.subject.decsCiclina D1-
dc.subject.decsImmunohistochemistry-
dc.subject.decsInmunohistoquímica-
dc.subject.decsLeprosy-
dc.subject.decsLepra-
dc.subject.decsNerve Fibers-
dc.subject.decsFibras Nerviosas-
dc.subject.decsReceptors, Notch-
dc.subject.decsReceptores Notch-
dc.subject.decsSignal Transduction-
dc.subject.decsTransducción de Señal-
dc.subject.decsSkin-
dc.subject.decsPiel-
dc.subject.decsTranscription Factor HES-1-
dc.subject.decsFactor de Transcripción HES-1-
dc.description.researchgroupidCOL0130733spa
oaire.awardnumberMinCiencias 727-2015spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D050676-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D019938-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D007150-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D007918-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D009412-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D051880-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D015398-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D012867-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000072056-
dc.relation.ispartofjournalabbrevFront. Immunol.spa
oaire.funderidentifier.rorRoR:03fd5ne08-
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