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Oligodendrocyte Progenitor Cells Become Regionally Diverse and Heterogeneous with Age

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dc.contributor.author Spitzer, Sonia Olivia
dc.contributor.author Sitnikov, Sergey
dc.contributor.author Kamen, Yasmine
dc.contributor.author Evans, Kimberley Anne
dc.contributor.author Kronenberg-Versteeg, Deborah
dc.contributor.author Dietmann, Sabine
dc.contributor.author de Faria, Omar
dc.contributor.author Agathou, Sylvia
dc.contributor.author Káradóttir, Ragnhildur Thóra
dc.date.accessioned 2023-03-02T01:03:28Z
dc.date.available 2023-03-02T01:03:28Z
dc.date.issued 2019-02-06
dc.identifier.citation Spitzer , S O , Sitnikov , S , Kamen , Y , Evans , K A , Kronenberg-Versteeg , D , Dietmann , S , de Faria , O , Agathou , S & Káradóttir , R T 2019 , ' Oligodendrocyte Progenitor Cells Become Regionally Diverse and Heterogeneous with Age ' , Neuron , vol. 101 , no. 3 , pp. 459-471.e5 . https://doi.org/10.1016/j.neuron.2018.12.020
dc.identifier.issn 0896-6273
dc.identifier.other 43318988
dc.identifier.other bca4a3ad-d639-43d3-a69a-6e1dfb67573d
dc.identifier.other 85060901253
dc.identifier.other 30654924
dc.identifier.uri https://hdl.handle.net/20.500.11815/4043
dc.description We thank J. Trotter (Johannes Gutenberg University, Mainz, Germany) for the NG2-EYFP mice, Dr. Moritz Matthey for help with minipump transplantation, Miss Mariann Kovacs with embryonic dissection, and Dr. Katrin Volbracht for critical comments on the work. We acknowledge the support of the Wellcome – MRC Cambridge Stem Cell Institute core facility managers, in particular for this work Dr. Maike Paramor and Miss Victoria Murray with RNA-seq, and all staff members of the University Biomedical Services (UBS). This project has received the following funding: funding from the European Research Council (ERC) under the European Union Horizon 2020 Research and Innovation Program (grant agreement 771411 to R.T.K. and K.A.E.), a Wellcome Trust research career development fellowship (091543/Z/10/Z to R.T.K. and K.A.E.) and studentship (102160/Z/13/Z to Y.K.), Paul G. Allen Frontiers Group Allen Distinguished Investigator Award 12076 (to R.T.K., D.K.-V., and K.A.E.), a Medical Research Council studentship (to S.O.S.), a Gates Cambridge Trust Gates scholarship (to S.S.), a Biotechnology and Biological Sciences Research Council studentship (to S.A.), a Homerton College Cambridge junior research fellowship (to D.K.-V.), UK MS Society Cambridge Myelin Repair Centre grant 50 (to R.T.K. and O.d.F.), a Fonds de Recherche du Québec - Santé scholarship (to Y.K.), a Cambridge Commonwealth, European and International Trust scholarship (to Y.K.), and a Lister Institute research prize (to R.T.K., K.A.E., and S.O.S.). Publisher Copyright: © 2018 The Author(s)
dc.description.abstract Spitzer et al. show that oligodendrocyte progenitor cells (OPCs) acquire ion channels and sensitivity to neuronal activity that differ between region and age. The onset and decline of ion channels follow developmental milestones. This heterogeneity indicates different functional states of OPCs.
dc.format.extent 4839955
dc.format.extent 459-471.e5
dc.language.iso en
dc.relation info:eu-repo/grantAgreement/EC/H2020/771411
dc.relation.ispartofseries Neuron; 101(3)
dc.rights info:eu-repo/semantics/openAccess
dc.subject bioelectricity
dc.subject differentiation
dc.subject electrophysiology
dc.subject glia
dc.subject glutamate
dc.subject ion channels
dc.subject myelin
dc.subject neurotransmitter receptors
dc.subject oligodendrocyte
dc.subject oligodendrocyte precursor cell
dc.subject General Neuroscience
dc.title Oligodendrocyte Progenitor Cells Become Regionally Diverse and Heterogeneous with Age
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1016/j.neuron.2018.12.020
dc.relation.url http://www.scopus.com/inward/record.url?scp=85060901253&partnerID=8YFLogxK
dc.contributor.department Faculty of Medicine


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