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dc.contributor.authorMuslimovic, Aida
dc.contributor.authorFriden, Vincent
dc.contributor.authorStarnberg, Karin
dc.contributor.authorTenstad, Olav
dc.contributor.authorEspedal, Heidi
dc.contributor.authorVukusic, Kristina
dc.contributor.authorNyström, Susanne
dc.contributor.authorWesén, Emelie
dc.contributor.authorEsbjörner, Elin K
dc.contributor.authorGranholm, Kristoffer
dc.contributor.authorLindahl, Bertil
dc.contributor.authorHammarsten, Ola
dc.date.accessioned2021-06-29T15:55:54Z
dc.date.available2021-06-29T15:55:54Z
dc.date.created2021-02-15T11:26:09Z
dc.date.issued2020
dc.identifier.issn0171-9335
dc.identifier.urihttps://hdl.handle.net/11250/2762421
dc.description.abstractBlood levels of cardiac troponins (cTn) and myoglobin are analysed when myocardial infarction (MI) is suspected. Here we describe a novel clearance mechanism for muscle proteins by muscle cells. The complete plasma clearance profile of cTn and myoglobin was followed in rats after intravenous or intermuscular injections and analysed by PET and fluorescence microscopy of muscle biopsies and muscle cells. Compared with intravenous injections, only 5 % of cTnT, 0.6 % of cTnI and 8 % of myoglobin were recovered in the circulation following intramuscular injection. In contrast, 47 % of the renal filtration marker FITC-sinistrin and 81 % of cTn fragments from MI-patients were recovered after intramuscular injection. In addition, PET and biopsy analysis revealed that cTn was taken up by the quadriceps muscle and both cTn and myoglobin were endocytosed by cultured muscle cells. This local clearance mechanism could possibly be the dominant clearance mechanism for cTn, myoglobin and other muscle damage biomarkers released by muscle cells.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleNovel clearance of muscle proteins by muscle cellsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2020 Elsevier GmbH.en_US
dc.source.articlenumber151127en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1016/j.ejcb.2020.151127
dc.identifier.cristin1889793
dc.source.journalEuropean Journal of Cell Biologyen_US
dc.relation.projectHelse Vest RHF: 911974en_US
dc.identifier.citationEuropean Journal of Cell Biology. 2020, 99 (8), 151127en_US
dc.source.volume99en_US
dc.source.issue8en_US


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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