Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/135801
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAndrés Benito, Pol-
dc.contributor.authorDomínguez González, Mayelín-
dc.contributor.authorFerrer, Isidro (Ferrer Abizanda)-
dc.date.accessioned2019-06-25T16:14:17Z-
dc.date.available2019-06-25T16:14:17Z-
dc.date.issued2018-07-27-
dc.identifier.issn1933-6896-
dc.identifier.urihttp://hdl.handle.net/2445/135801-
dc.description.abstractTargeted expression of genes coding for proteins specific to astrocytes, oligodendrocytes and myelin was performed in frontal cortex area 8 of Creutzfeldt-Jakob disease methionine/methionine and valine/valine (CJD MM1 and VV2, respectively) compared with controls. GFAP (glial fibrillary acidic protein) mRNA was up-regulated whereas SLC1A2 (solute carrier family 1 member 2, coding for glutamate transporter 1: GLT1), AQ4 (aquaporin 4), MPC1 (mitochondrial pyruvate carrier 1) and UCP5 (mitochondrial uncoupled protein 5) mRNAs were significantly down-regulated in CJD MM1 and CJD VV2, and GJA1 (connexin 43) in CJD VV2. OLIG1 and OLIG2 (oligodendocyte transcription factor 1 and 2, respectively), SOX10 (SRY-Box10) and oligodendroglial precursor cell (OPC) marker NG2 (neuronal/glial antigen) 2 were preserved, but GALC (coding for galactosylceramidase), SLC2A1 (solute carrier family 2 member 1: glucose transporter member 1: GLUT1) and MCT1 (monocarboxylic acid transporter 1) mRNA expression levels were significantly reduced in CJD MM1 and CJD VV2. Expression levels of most genes linked to myelin were not altered in the cerebral cortex in CJD. Immunohistochemistry to selected proteins disclosed individual variations but GFAP, Olig-2, AQ4 and GLUT1 correlated with mRNA levels, whereas GLT1 was subjected to individual variations. However, MPC1, UCP5 and MCT1 decrease was more closely related to the respective reduced neuronal immunostaining. These observations support the idea that molecular deficits linked to energy metabolism and solute transport in astrocytes and oligodendrocytes, in addition to neurons, are relevant in the pathogenesis of cortical lesions in CJD.-
dc.format.extent10 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherLandes Bioscience-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1080/19336896.2018.1500076-
dc.relation.ispartofPrion, 2018, vol. 12, num. 3-4, p. 216-225-
dc.relation.urihttps://doi.org/10.1080/19336896.2018.1500076-
dc.rights(c) Andrés Benito, Pol et al., 2018-
dc.subject.classificationMalaltia de Creutzfeldt-Jakob-
dc.subject.classificationMalalties per prions-
dc.subject.classificationAstròcits-
dc.subject.classificationLòbul frontal-
dc.subject.classificationFactors de transcripció-
dc.subject.otherCreutzfeldt-Jakob disease-
dc.subject.otherPrion diseases-
dc.subject.otherAstrocytes-
dc.subject.otherFrontal lobe-
dc.subject.otherTranscription factors-
dc.titleAltered gene transcription linked to astrocytes and oligodendrocytes in frontal cortex in Creutzfeldt-Jakob disease-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec689455-
dc.date.updated2019-06-25T16:14:17Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Patologia i Terapèutica Experimental)

Files in This Item:
File Description SizeFormat 
689455.pdf1.28 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.