Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106507
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dc.contributor.authorFloriddia, Elisa M.-
dc.contributor.authorLourenço, Tânia-
dc.contributor.authorZhang, Shupei-
dc.contributor.authorvan Bruggen, David-
dc.contributor.authorHilscher, Markus M.-
dc.contributor.authorKukanja, Petra-
dc.contributor.authorGonçalves Dos Santos, João P.-
dc.contributor.authorAltınkök, Müge-
dc.contributor.authorYokota, Chika-
dc.contributor.authorLlorens-Bobadilla, Enric-
dc.contributor.authorMulinyawe, Sara B-
dc.contributor.authorGrãos, Mário-
dc.contributor.authorSun, Lu O.-
dc.contributor.authorFrisén, Jonas-
dc.contributor.authorNilsson, Mats-
dc.contributor.authorCastelo-Branco, Gonçalo-
dc.date.accessioned2023-04-05T12:17:16Z-
dc.date.available2023-04-05T12:17:16Z-
dc.date.issued2020-11-17-
dc.identifier.issn2041-1723pt
dc.identifier.urihttps://hdl.handle.net/10316/106507-
dc.description.abstractMature oligodendrocytes (MOLs) show transcriptional heterogeneity, the functional consequences of which are unclear. MOL heterogeneity might correlate with the local environment or their interactions with different neuron types. Here, we show that distinct MOL populations have spatial preference in the mammalian central nervous system (CNS). We found that MOL type 2 (MOL2) is enriched in the spinal cord when compared to the brain, while MOL types 5 and 6 (MOL5/6) increase their contribution to the OL lineage with age in all analyzed regions. MOL2 and MOL5/6 also have distinct spatial preference in the spinal cord regions where motor and sensory tracts run. OL progenitor cells (OPCs) are not specified into distinct MOL populations during development, excluding a major contribution of OPC intrinsic mechanisms determining MOL heterogeneity. In disease, MOL2 and MOL5/6 present different susceptibility during the chronic phase following traumatic spinal cord injury. Our results demonstrate that the distinct MOL populations have different spatial preference and different responses to disease.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.relationKarolinska Institutept
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshAnimalspt
dc.subject.meshAxonspt
dc.subject.meshBasic Helix-Loop-Helix Leucine Zipper Transcription Factorspt
dc.subject.meshBiomarkerspt
dc.subject.meshCell Lineagept
dc.subject.meshCorpus Callosumpt
dc.subject.meshEncephalomyelitis, Autoimmune, Experimentalpt
dc.subject.meshFemalept
dc.subject.meshGene Expression Profilingpt
dc.subject.meshMice, Inbred C57BLpt
dc.subject.meshMice, Inbred CBApt
dc.subject.meshMice, Knockoutpt
dc.subject.meshMice, Transgenicpt
dc.subject.meshOligodendrogliapt
dc.subject.meshSingle-Cell Analysispt
dc.subject.meshSpinal Cordpt
dc.subject.meshSpinal Cord Injuriespt
dc.titleDistinct oligodendrocyte populations have spatial preference and different responses to spinal cord injurypt
dc.typearticle-
degois.publication.firstPage5860pt
degois.publication.issue1pt
degois.publication.titleNature Communicationspt
dc.peerreviewedyespt
dc.identifier.doi10.1038/s41467-020-19453-xpt
degois.publication.volume11pt
dc.date.embargo2020-11-17*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.orcid0000-0002-2707-1488-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons