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dc.rights.licenseopenen_US
dc.contributor.authorSCHWEIGERT, Olga
dc.contributor.authorADLER, Julia
dc.contributor.authorLANGST, Nathalie
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorAISSI, Dylan
dc.contributor.authorDUQUE ESCOBAR, Jorge
dc.contributor.authorTONG, Teng
dc.contributor.authorMULLER, Christian
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorTREGOUET, David-Alexandre
dc.contributor.authorLUKOWSKI, Robert
dc.contributor.authorZELLER, Tanja
dc.date.accessioned2021-05-12T15:37:10Z
dc.date.available2021-05-12T15:37:10Z
dc.date.issued2021-03-30
dc.identifier.issn1470-8736 (Electronic) 0143-5221 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/74553
dc.description.abstractEnHypertension is a complex and multifactorial disorder caused by lifestyle and environmental factors, inflammation and disease-related genetic factors and is a risk factor for stroke, ischemic heart disease and renal failure. Although circulating monocytes and tissue macrophages contribute to the pathogenesis of hypertension, the underlying mechanisms are poorly understood. Cysteine rich protein 1 (CRIP1) is highly expressed in immune cells, and CRIP1 mRNA expression in monocytes associates with blood pressure (BP) and is upregulated by proinflammatory modulation suggesting a link between CRIP1 and BP regulation through the immune system. To address this functional link, we studied CRIP1 expression in immune cells in relation to BP using a human cohort study and hypertensive mouse models. CRIP1 expression in splenic monocytes/macrophages and in circulating monocytes was significantly affected by angiotensin II (Ang II) in a BP-elevating dose (2 mg/kg/day). In the human cohort study, monocytic CRIP1 expression levels were associated with elevated BP, whereas upon differentiation of monocytes to macrophages this association along with the CRIP1 expression level was diminished. In conclusion, CRIP1-positive circulating and splenic monocytes seem to play an important role in hypertension related inflammatory processes through endogenous hormones such as Ang II. These findings suggest that CRIP1 may affect the interaction between the immune system, in particular monocytes, and the pathogenesis of hypertension.
dc.language.isoENen_US
dc.subject.enAngiotensin converting enzyme 2
dc.subject.enBlood pressure
dc.subject.enHypertension
dc.subject.enImmunsystem
dc.subject.enRenin-angiotensin system
dc.title.enCRIP1 expression in monocytes related to hypertension
dc.typeArticle de revueen_US
dc.identifier.doi10.1042/CS20201372en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed33782695en_US
bordeaux.journalClinical Scienceen_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamVINTAGEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03225628
hal.version1
hal.date.transferred2021-05-12T15:37:14Z
hal.exporttrue
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