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DC Field | Value | Language |
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dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | RAABE, Florian J. | |
dc.contributor.author | GALINSKI, Sabrina | |
dc.contributor.author | PAPIOL, Sergi | |
dc.contributor.author | FALKAI, Peter G. | |
dc.contributor.author | SCHMITT, Andrea | |
dc.contributor.author | ROSSNER, Moritz J. | |
dc.date.accessioned | 2019-05-30T13:51:39Z | |
dc.date.available | 2019-05-30T13:51:39Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | NPJ SCHIZOPHRENIA, v.4, article ID 23, 11p, 2018 | |
dc.identifier.issn | 2334-265X | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/32011 | |
dc.description.abstract | Postmortem studies in patients with schizophrenia (SCZ) have revealed deficits in myelination, abnormalities in myelin gene expression and altered numbers of oligodendrocytes in the brain. However, gaining mechanistic insight into oligodendrocyte (OL) dysfunction and its contribution to SCZ has been challenging because of technical hurdles. The advent of individual patient-derived human-induced pluripotent stem cells (hiPSCs), combined with the generation of in principle any neuronal and glial cell type, including OLs and oligodendrocyte precursor cells (OPCs), holds great potential for understanding the molecular basis of the aetiopathogenesis of genetically complex psychiatric diseases such as SCZ and could pave the way towards personalized medicine. The development of neuronal and glial co-culture systems now appears to enable the in vitro study of SCZ-relevant neurobiological endophenotypes, including OL dysfunction and myelination, with unprecedented construct validity. Nonetheless, the meaningful stratification of patients before the subsequent functional analyses of patient-derived cell systems still represents an important bottleneck. Here, to improve the predictive power of ex vivo disease modelling we propose using hiPSC technology to focus on representatives of patient subgroups stratified for genomic and/or phenomic features and neurobiological cell systems. Therefore, this review will outline the evidence for the involvement of OPCs/OLs in SCZ in the context of their proposed functions, including myelination and axon support, the implications for hiPSC-based cellular disease modelling and potential strategies for patient selection. | eng |
dc.description.sponsorship | German Research Foundation [SPP Glia RO 4076/3-1] | |
dc.description.sponsorship | German Research Foundation (PsyCourse) [FKZ RO 4076/5-1, RO 241/16-1] | |
dc.description.sponsorship | Else Kroner-Fresenius Foundation | |
dc.language.iso | eng | |
dc.publisher | SPRINGERNATURE | eng |
dc.relation.ispartof | Npj Schizophrenia | |
dc.rights | openAccess | eng |
dc.subject.other | pluripotent stem-cells | eng |
dc.subject.other | white-matter | eng |
dc.subject.other | polygenic risk | eng |
dc.subject.other | psychiatric-disorders | eng |
dc.subject.other | efficient generation | eng |
dc.subject.other | 1st episode | eng |
dc.subject.other | directed differentiation | eng |
dc.subject.other | cognitive deficits | eng |
dc.subject.other | brain-development | eng |
dc.subject.other | gene-expression | eng |
dc.title | Studying and modulating schizophrenia-associated dysfunctions of oligodendrocytes with patient-specific cell systems | eng |
dc.type | article | eng |
dc.rights.holder | Copyright SPRINGERNATURE | eng |
dc.identifier.doi | 10.1038/s41537-018-0066-4 | |
dc.identifier.pmid | 30451850 | |
dc.subject.wos | Psychiatry | eng |
dc.type.category | review | eng |
dc.type.version | publishedVersion | eng |
hcfmusp.author.external | RAABE, Florian J.:Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Psychiat & Psychotherapy, Mol & Behav Neurobiol, Munich, Germany; IMPRS TP, Munich, Germany | |
hcfmusp.author.external | GALINSKI, Sabrina:Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Psychiat & Psychotherapy, Mol & Behav Neurobiol, Munich, Germany | |
hcfmusp.author.external | PAPIOL, Sergi:Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Psychiat & Psychotherapy, Mol & Behav Neurobiol, Munich, Germany; Ludwig Maximilians Univ Munchen, Univ Hosp, IPPG, Munich, Germany | |
hcfmusp.author.external | FALKAI, Peter G.:Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Psychiat & Psychotherapy, Mol & Behav Neurobiol, Munich, Germany | |
hcfmusp.author.external | ROSSNER, Moritz J.:Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Psychiat & Psychotherapy, Mol & Behav Neurobiol, Munich, Germany | |
hcfmusp.description.articlenumber | 23 | |
hcfmusp.description.volume | 4 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.id | WOS:000461475200001 | |
hcfmusp.origem.id | 2-s2.0-85057208757 | |
hcfmusp.publisher.city | LONDON | eng |
hcfmusp.publisher.country | ENGLAND | eng |
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dc.description.index | PubMed | eng |
hcfmusp.citation.scopus | 25 | - |
hcfmusp.scopus.lastupdate | 2024-03-29 | - |
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