Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-274
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dc.contributor.authorKiouptsi, Klytaimnistra-
dc.contributor.authorFinger, Stefanie-
dc.contributor.authorGarlapati, Venkata S.-
dc.contributor.authorKnorr, Maike-
dc.contributor.authorBrandt, Moritz-
dc.contributor.authorWalter, Ulrich-
dc.contributor.authorWenzel, Philip-
dc.contributor.authorReinhardt, Christoph-
dc.date.accessioned2019-01-08T15:26:33Z-
dc.date.available2019-01-08T16:26:33Z-
dc.date.issued2019-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/276-
dc.description.abstractThe prototypic protein disulfide isomerase (PDI), encoded by the P4HB gene, has been described as a survival factor in ischemic cardiomyopathy. However, the role of protein disulfide isomerase associated 6 (PDIA6) under hypoxic conditions in the myocardium remains enigmatic, and it is unknown whether the gut microbiota influences the expression of PDI and PDIA6 under conditions of acute myocardial infarction. Here, we revealed that, in addition to the prototypic PDI, the PDI family member PDIA6, a regulator of the unfolded protein response, is upregulated in the mouse cardiomyocyte cell line HL-1 when cultured under hypoxia. In vivo, in the left anterior descending artery (LAD) ligation mouse model of acute myocardial infarction, similar to PDI, PDIA6 protein expression was enhanced in the infarcted area (LAD ) relative to uninfarcted sham tissue or the neighbouring area at risk (LAD–) of C57BL/6J mice. Interestingly, we found that ex-germ-free (ex-GF) mice subjected to the LAD ligation model for 24 h had a reduced ejection fraction compared with their conventionally raised (CONV-R) SPF controls. Furthermore, the LAD area in the infarcted heart of ex-GF mice showed reduced PDIA6 expression relative to CONV-R controls, suggesting that the presence of a gut microbiota enhanced LAD ligation-triggered PDIA6 expression. Collectively, our results demonstrate that PDIA6 is upregulated in cardiomyocytes as a consequence of hypoxia. In the LAD mouse model, PDIA6 was also increased in the infarcted area under in vivo conditions, but this increase was suppressed in ex-GF mice relative to CONV-R controls.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin-
dc.language.isoeng-
dc.rightsCC BYde_DE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleHypoxia evokes increased PDI and PDIA6 expression in the infarcted myocardium of ex-germ-free and conventionally raised miceen_GB
dc.typeZeitschriftenaufsatzde_DE
dc.identifier.urnurn:nbn:de:hebis:77-publ-587638-
dc.identifier.doihttp://doi.org/10.25358/openscience-274-
jgu.type.dinitypearticle-
jgu.type.versionPublished versionen_GB
jgu.type.resourceText-
jgu.organisation.departmentFB 04 Medizin-
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleBiology open-
jgu.journal.volume8-
jgu.journal.issue1-
jgu.pages.alternativebio038851-
jgu.publisher.year2019-
jgu.publisher.nameCompany-
jgu.publisher.placeCambridge-
jgu.publisher.urihttp://dx.doi.org/10.1242/bio.038851-
jgu.publisher.issn2046-6390-
jgu.organisation.placeMainz-
jgu.subject.ddccode610-
opus.date.accessioned2019-01-08T15:26:33Z-
opus.date.modified2019-01-22T10:01:12Z-
opus.date.available2019-01-08T16:26:33-
opus.subject.dfgcode00-000-
opus.organisation.stringFB 04: Medizin: Centrum für Thrombose und Hämostase (CTH)de_DE
opus.organisation.stringFB 04: Medizin: Zentrum für Kardiologiede_DE
opus.identifier.opusid58763-
opus.institute.number0463-
opus.institute.number0466-
opus.metadataonlyfalse-
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_GB
opus.affiliatedKiouptsi, Klytaimnistra-
opus.affiliatedFinger, Stefanie-
opus.affiliatedGarlapati, Venkata S.-
opus.affiliatedKnorr, Maike-
opus.affiliatedBrandt, Moritz-
opus.affiliatedWalter, Ulrich-
opus.affiliatedWenzel, Philip-
opus.affiliatedReinhardt, Christoph-
jgu.publisher.doi10.1242/bio.038851
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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