Amyotrophic lateral sclerosis, gene deregulation in the anterior horn of the spinal cord and frontal cortex area 8: implications in frontotemporal lobar degeneration

dc.contributor.authorAndrés Benito, Pol
dc.contributor.authorMoreno Castro, Jesús
dc.contributor.authorAso Pérez, Ester
dc.contributor.authorPovedano, Mònica
dc.contributor.authorFerrer, Isidro (Ferrer Abizanda)
dc.date.accessioned2018-09-12T09:58:10Z
dc.date.available2018-09-12T09:58:10Z
dc.date.issued2017-03-01
dc.date.updated2018-07-24T12:10:22Z
dc.description.abstractTranscriptome arrays identifies 747 genes differentially expressed in the anterior horn of the spinal cord and 2,300 genes differentially expressed in frontal cortex area 8 in a single group of typical sALS cases without frontotemporal dementia compared with age-matched controls. Main up-regulated clusters in the anterior horn are related to inflammation and apoptosis; down-regulated clusters are linked to axoneme structures and protein synthesis. In contrast, up-regulated gene clusters in frontal cortex area 8 involve neurotransmission, synaptic proteins and vesicle trafficking, whereas main down-regulated genes cluster into oligodendrocyte function and myelin-related proteins. RT-qPCR validates the expression of 58 of 66 assessed genes from different clusters. The present results: a. reveal regional differences in de-regulated gene expression between the anterior horn of the spinal cord and frontal cortex area 8 in the same individuals suffering from sALS; b. validate and extend our knowledge about the complexity of the inflammatory response in the anterior horn of the spinal cord; and c. identify for the first time extensive gene up-regulation of neurotransmission and synaptic-related genes, together with significant down-regulation of oligodendrocyte-and myelin-related genes, as important contributors to the pathogenesis of frontal cortex alterations in the sALS/frontotemporal lobar degeneration spectrum complex at stages with no apparent cognitive impairment.
dc.format.extent29 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec686635
dc.identifier.pmid28283675
dc.identifier.urihttps://hdl.handle.net/2445/124465
dc.language.isoeng
dc.publisherImpact Journals
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.18632/aging.101195
dc.relation.ispartofAging, 2017, vol. 9, num. 3, P. 823-851
dc.relation.urihttps://doi.org/10.18632/aging.101195
dc.rightscc by (c) Andrés Benito et al., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationExpressió gènica
dc.subject.classificationEsclerosi lateral amiotròfica
dc.subject.otherGene expression
dc.subject.otherAmyotrophic lateral sclerosis
dc.titleAmyotrophic lateral sclerosis, gene deregulation in the anterior horn of the spinal cord and frontal cortex area 8: implications in frontotemporal lobar degeneration
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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