Genetic inhibition of CARD9 accelerates the development of atherosclerosis in mice through CD36 dependent-defective autophagy.
Yujiao ZhangMarie VandestienneJean-Rémi LavillegrandJeremie JoffreIcia Santos-ZasAonghus LavelleXiaodan ZhongWilfried Le GoffMaryse GuérinRida Al-RifaiLudivine LauransPatrick BrunevalCoralie L GuerinMarc DiedisheimMélanie MigaudAnne PuelFanny LanternierJean-Laurent CasanovaClément CochainAlma ZerneckeAntoine-Emmanuel SalibaMichal MokryJean-Sébastien SilvestreAlain TedguiZiad MallatSoraya TalebOlivia LenoirCécile VindisStéphane M CamusHarry SokolHafid Ait OufellaPublished in: Nature communications (2023)
Caspase recruitment-domain containing protein 9 (CARD9) is a key signaling pathway in macrophages but its role in atherosclerosis is still poorly understood. Global deletion of Card9 in Apoe -/- mice as well as hematopoietic deletion in Ldlr -/- mice increases atherosclerosis. The acceleration of atherosclerosis is also observed in Apoe -/- Rag2 -/- Card9 -/- mice, ruling out a role for the adaptive immune system in the vascular phenotype of Card9 deficient mice. Card9 deficiency alters macrophage phenotype through CD36 overexpression with increased IL-1β production, increased lipid uptake, higher cell death susceptibility and defective autophagy. Rapamycin or metformin, two autophagy inducers, abolish intracellular lipid overload, restore macrophage survival and autophagy flux in vitro and finally abolish the pro-atherogenic effects of Card9 deficiency in vivo. Transcriptomic analysis of human CARD9-deficient monocytes confirms the pathogenic signature identified in murine models. In summary, CARD9 is a key protective pathway in atherosclerosis, modulating macrophage CD36-dependent inflammatory responses, lipid uptake and autophagy.
Keyphrases
- cell death
- signaling pathway
- cardiovascular disease
- endoplasmic reticulum stress
- oxidative stress
- adipose tissue
- high fat diet induced
- induced apoptosis
- cell cycle arrest
- pi k akt
- endothelial cells
- fatty acid
- cell proliferation
- transcription factor
- metabolic syndrome
- type diabetes
- dendritic cells
- immune response
- single cell
- rna seq
- genome wide
- peripheral blood
- amino acid
- replacement therapy
- dna methylation
- binding protein
- reactive oxygen species