Glial Control of Synapse Number in Healthy and Diseased Brain

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dc.contributor.authorLee, Eunbeolko
dc.contributor.authorChung, Won-Sukko
dc.date.accessioned2019-03-19T01:25:19Z-
dc.date.available2019-03-19T01:25:19Z-
dc.date.created2019-03-04-
dc.date.created2019-03-04-
dc.date.issued2019-02-
dc.identifier.citationFRONTIERS IN CELLULAR NEUROSCIENCE, v.13-
dc.identifier.issn1662-5102-
dc.identifier.urihttp://hdl.handle.net/10203/251623-
dc.description.abstractGlial cells are emerging as crucial players that mediate development and homeostasis of the central nervous system (CNS). In particular, glial cells are closely associated with synapses, and control synapse formation, function, plasticity, and elimination during the stages of development and adulthood. Importantly, it is now increasingly evident that abnormal glial function can be an active inducer of the initiation and progression of various neurodegenerative diseases. Here, we discuss recent developments on the physiological roles of glial cells in the brain, and propose that synapse loss, which is a common characteristic of several neurodegenerative diseases, can be initiated by mis-regulation of normal glial function.-
dc.languageEnglish-
dc.publisherFRONTIERS MEDIA SA-
dc.titleGlial Control of Synapse Number in Healthy and Diseased Brain-
dc.typeArticle-
dc.identifier.wosid000458744400001-
dc.identifier.scopusid2-s2.0-85064197613-
dc.type.rimsART-
dc.citation.volume13-
dc.citation.publicationnameFRONTIERS IN CELLULAR NEUROSCIENCE-
dc.identifier.doi10.3389/fncel.2019.00042-
dc.contributor.localauthorChung, Won-Suk-
dc.description.isOpenAccessY-
dc.type.journalArticleReview-
dc.subject.keywordAuthorastrocytes-
dc.subject.keywordAuthormicroglia-
dc.subject.keywordAuthorsynapse loss-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorneurodegenerative diseases-
dc.subject.keywordPlusASTROCYTE-SECRETED PROTEINS-
dc.subject.keywordPlusAMYLOID-BETA OLIGOMERS-
dc.subject.keywordPlusLONG-TERM POTENTIATION-
dc.subject.keywordPlusMOUSE MODEL-
dc.subject.keywordPlusREACTIVE ASTROCYTES-
dc.subject.keywordPlusALPHA-SYNUCLEIN-
dc.subject.keywordPlusTHALAMOCORTICAL SYNAPSES-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusCNS SYNAPTOGENESIS-
dc.subject.keywordPlusTRPA1 CHANNELS-
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