Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-8053
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dc.contributor.authorMaus, Frank-
dc.contributor.authorSakry, Dominik-
dc.contributor.authorBinamé, Fabien-
dc.contributor.authorKarram, Khalad-
dc.contributor.authorRajalingam, Krishnaraj-
dc.contributor.authorWatts, Colin-
dc.contributor.authorHeywood, Richard-
dc.contributor.authorKrüger, Rejko-
dc.contributor.authorStegmüller, Judith-
dc.contributor.authorWerner, Hauke B.-
dc.contributor.authorNave, Klaus-Armin-
dc.contributor.authorAlbers, Eva-Maria-
dc.contributor.authorTrotter, Jacqueline-
dc.date.accessioned2022-10-17T07:29:50Z-
dc.date.available2022-10-17T07:29:50Z-
dc.date.issued2015
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8068-
dc.description.abstractThe NG2 proteoglycan is characteristically expressed by oligodendrocyte progenitor cells (OPC) and also by aggressive brain tumours highly resistant to chemo- and radiation therapy. Oligodendrocyte-lineage cells are particularly sensitive to stress resulting in cell death in white matter after hypoxic or ischemic insults of premature infants and destruction of OPC in some types of Multiple Sclerosis lesions. Here we show that the NG2 proteoglycan binds OMI/HtrA2, a mitochondrial serine protease which is released from damaged mitochondria into the cytosol in response to stress. In the cytosol, OMI/HtrA2 initiates apoptosis by proteolytic degradation of anti-apoptotic factors. OPC in which NG2 has been downregulated by siRNA, or OPC from the NG2-knockout mouse show an increased sensitivity to oxidative stress evidenced by increased cell death. The proapoptotic protease activity of OMI/HtrA2 in the cytosol can be reduced by the interaction with NG2. Human glioma expressing high levels of NG2 are less sensitive to oxidative stress than those with lower NG2 expression and reducing NG2 expression by siRNA increases cell death in response to oxidative stress. Binding of NG2 to OMI/HtrA2 may thus help protect cells against oxidative stress-induced cell death. This interaction is likely to contribute to the high chemo- and radioresistance of glioma.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizinde
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc570 Biowissenschaftende_DE
dc.subject.ddc570 Life sciencesen_GB
dc.titleThe NG2 proteoglycan protects oligodendrocyte precursor cells against oxidative stress via interaction with OMI/HtrA2en_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-8053-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 10 Biologiede
jgu.organisation.number7970-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titlePLoS onede
jgu.journal.volume10de
jgu.journal.issue9de
jgu.pages.alternativee0137311de
jgu.publisher.year2015-
jgu.publisher.namePLoSde
jgu.publisher.placeLawrence, Kan.de
jgu.publisher.urihttp://dx.doi.org/10.1371/journal.pone.0137311de
jgu.publisher.issn1932-6203de
jgu.notes.publicAlbers, Eva-Maria veröffentlicht auch unter Krämer-Albers, Eva-Mariade
jgu.organisation.placeMainz-
jgu.subject.ddccode570de
opus.date.modified2018-09-05T09:12:01Z
opus.subject.dfgcode00-000
opus.organisation.stringFB 10: Biologie: Abteilung Molekulare Zellbiologie / Biologie für Medizinerde_DE
opus.identifier.opusid51966
opus.institute.number1004
opus.metadataonlyfalse
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_EN
opus.affiliatedAlbers, Eva-Maria
opus.affiliatedTrotter, Jacqueline
jgu.publisher.doi10.1371/journal.pone.0137311de
jgu.organisation.rorhttps://ror.org/023b0x485-
Appears in collections:DFG-OA-Publizieren (2012 - 2017)

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