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dc.rights.licenseopenen_US
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorFOUSSARD, Ninon
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorBOURGUIGNON, Célia
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorGROUTHIER, Virginie
dc.contributor.authorCARADU, Caroline
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorCHAPOULY, Candice
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorGADEAU, Alain-Pierre
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorCOUFFINHAL, Thierry
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorRENAULT, Marie-Ange
dc.date.accessioned2025-02-10T09:16:04Z
dc.date.available2025-02-10T09:16:04Z
dc.date.issued2025-01-18
dc.identifier.issn1475-2840en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/204775
dc.description.abstractEnChronic Limb-Threatening Ischemia (CLTI) represents the most advanced stage of Peripheral Artery Disease (PAD) and is associated with dire prognosis, characterized by a substantial risk of limb amputation and diminished life expectancy. Despite significant advancements in therapeutic interventions, the underlying mechanisms precipitating the progression of PAD to CLTI remain elusive. Considering diabetes is one of the main risk factors contributing to PAD exacerbation into CLTI, we compared hind limb ischemia recovery in HFD STZ vs. non-HFD STZ mice to identify new mechanisms responsible for the exacerbation of PAD. We used three different mouse models of diabetes and found that blood flow recovery in HFD STZ mice is altered only from day 14 post-surgery. Consistent with this kinetics, we found that angiogenesis and myogenesis which typically occur between day five and day 14 post-surgery are not impaired in mice in which diabetes was induced by a high fat diet and streptozotocin injections (HFD STZ mice). On the contrary, we found that capillary functionality e.i. acquisition of functional intercellular junctions and immune quiescence is impaired in HFD + STZ mice. Notably, 28 days after hind limb ischemia surgery, HFD + STZ mice display significantly increased capillary permeability to IgG and significantly increased levels of ICAM1. This was associated with an increased macrophage infiltration and an impaired myocyte differentiation. Importantly, we used ICAM1-blocking antibodies to demonstrate that increased ICAM1 expression in HFD + STZ mice decreases white blood cell circulation velocity within the microcirculation, which impairs its perfusion. Notably anti-ICAM1 therapy did diminish macrophage infiltration and oxidative stress but not myopathy suggesting that myopathy characterized by small myocytes expressing higher level of MYH2 could be responsible for microangiopathy. ICAM1 expression by the microvasculature impairs ischemic muscle reperfusion in HFD + STZ mice. Importantly, the increase in blood flow between day 14 and day 90 post-HLI surgery is not associated with an increased capillary density but with an improved functionality of capillaries.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAnimals
dc.subject.enDiabetes Mellitus
dc.subject.enExperimental
dc.subject.enMuscle
dc.subject.enSkeletal
dc.subject.enIntercellular Adhesion Molecule-1
dc.subject.enMice
dc.subject.enInbred C57BL
dc.subject.enMale
dc.subject.enHindlimb
dc.subject.enRegional Blood Flow
dc.subject.enNeovascularization
dc.subject.enPhysiologic
dc.subject.enTime Factors
dc.subject.enCapillary Permeability
dc.subject.enReperfusion Injury
dc.subject.enDiet
dc.subject.enHigh-Fat
dc.subject.enMice
dc.subject.enPeripheral Arterial Disease
dc.subject.enIschemia
dc.subject.enChronic Limb-Threatening Ischemia
dc.subject.enOxidative Stress
dc.title.enICAM1 blockade improves ischemic muscle reperfusion in diabetic mice.
dc.title.alternativeCardiovasc Diabetolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s12933-025-02573-3en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologie/Cardiologie et système cardiovasculaireen_US
dc.identifier.pubmed39827135en_US
bordeaux.journalCardiovascular Diabetologyen_US
bordeaux.page20en_US
bordeaux.volume24en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04937546
hal.version1
hal.date.transferred2025-02-10T09:16:07Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Cardiovascular%20Diabetology&rft.date=2025-01-18&rft.volume=24&rft.issue=1&rft.spage=20&rft.epage=20&rft.eissn=1475-2840&rft.issn=1475-2840&rft.au=FOUSSARD,%20Ninon&BOURGUIGNON,%20C%C3%A9lia&GROUTHIER,%20Virginie&CARADU,%20Caroline&CHAPOULY,%20Candice&rft.genre=article


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