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dc.contributor.authorWalter, J
dc.contributor.authorKemmerling, N
dc.contributor.authorWunderlich, P
dc.contributor.authorGlebov, Konstantin
dc.contributor.editorBehl C
dc.date.accessioned2019-01-30T12:47:54Z
dc.date.available2019-01-30T12:47:54Z
dc.date.issued2017-11
dc.identifier.issn0022-3042
dc.identifier.issn1471-4159
dc.identifier.urihttp://hdl.handle.net/10026.1/13236
dc.description.abstract

<jats:title>Abstract</jats:title><jats:sec><jats:label /><jats:p>γ‐Secretase is an intramembrane cleaving protease involved in the generation of the Alzheimer's disease (<jats:styled-content style="fixed-case">AD</jats:styled-content>)‐associated amyloid β peptide (Aβ). γ‐Secretase is ubiquitously expressed in different organs, and also in different cell types of the human brain. Besides the involvement in the proteolytic generation of Aβ from the amyloid precursor protein, γ‐secretase cleaves many additional protein substrates, suggesting pleiotropic functions under physiological and pathophysiological conditions. Microglia exert important functions during brain development and homeostasis in adulthood, and accumulating evidence indicates that microglia and neuroinflammatory processes contribute to the pathogenesis of neurodegenerative diseases. Recent studies demonstrate functional implications of γ‐secretase in microglia, suggesting that alterations in γ‐secretase activity could contribute to <jats:styled-content style="fixed-case">AD</jats:styled-content> pathogenesis by modulation of microglia and related neuroinflammatory processes during neurodegeneration. In this review, we discuss the involvement of γ‐secretase in the regulation of microglial functions, and the potential relevance of these processes under physiological and pathophysiological conditions.</jats:p></jats:sec><jats:sec><jats:label /><jats:p> <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/jnc14224-fig-0004-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text> </jats:p><jats:p><jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1471-4159/homepage/virtual_issues.htm#Amyloid">This article is part of the series “Beyond Amyloid”</jats:ext-link>.</jats:p></jats:sec>

dc.format.extent445-454
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherWiley
dc.subjectephrin
dc.subjectmicroglia
dc.subjectnotch
dc.subjectpresenilin
dc.subjectproteolytic processing
dc.subjectsecretase
dc.subjectTREM2
dc.titleγ-Secretase in microglia - implications for neurodegeneration and neuroinflammation
dc.typejournal-article
dc.typeJournal Article
dc.typeReview
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000415368800006&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue4
plymouth.volume143
plymouth.publication-statusPublished
plymouth.journalJournal of Neurochemistry
dc.identifier.doi10.1111/jnc.14224
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2017-09-18
dc.identifier.eissn1471-4159
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1111/jnc.14224
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-11
rioxxterms.typeJournal Article/Review


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