Journal of the American Heart Association · 2025
Interleukin-1 Signaling on Vascular Smooth Muscle Cells Accelerates Atherosclerosis in a Murine Model of Kawasaki Disease.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Chen Shuang, Savas Asli, Atici Asli, Lee Youngho, Lane Malcolm, Aubuchon Emily, Moreira Debbie, Hsu-Wilbraham Alexander, Shimada Kenichi, Crother Timothy R, Noval Rivas Magali, Arditi Moshe
Аннотация
BACKGROUND: We previously showed that Lactobacillus casei cell wall extract-induced Kawasaki disease (KD) vasculitis significantly accelerates atherosclerosis in hypercholesterolemic mice on high-fat diet. Here, we investigated the contribution of IL-1 (interleukin-1) signaling on vascular smooth muscle cells in this model.
METHODS: Tamoxifen-inducible vascular smooth muscle cell-specific IL-1 receptor (Il1r1) knockout (SMCΔ/Δ) mice and Il1r1SMCWT/WT [wildtype/wildtype] littermate controls, all on ApoE-/- background, were injected with either PBS or Lactobacillus casei cell wall extract. Two weeks later, mice were fed a tamoxifen diet for 2 weeks to induce Il1r1 deletion on vascular smooth muscle cells before being exposed to 8 weeks of Western diet to promote atherosclerosis.
RESULTS: KD vasculitis led to a significant acceleration of atherosclerosis. Il1r1SMCΔ/Δ mice had significantly diminished atherosclerotic plaque size, macrophage infiltration, and necrotic core formation in the aortic root, as well as diminished lipid accumulation in the aorta en face compared with control mice, despite similar serum cholesterol levels. Il1r1SMCΔ/Δ mice also had significantly diminished expression of endothelial adhesion molecules VCAM-1 (vascular cell adhesion molecule 1) and ICAM-1 (intercellular adhesion molecule 1) in the lesion area, as well as reduced serum MCP-1 (monocyte chemotaxis protein-1) levels compared with Il1r1SMCWT/WT control mice. Monocyte and macrophage recruitment was significantly reduced in the Il1r1SMCΔ/Δ group compared with the Il1r1SMCWT/WT group.
CONCLUSIONS: Our results suggest an important pathophysiologic link between IL-1 signaling on vascular smooth muscle cells and subsequent acceleration of atherosclerosis in hypercholesterolemic mice following KD vasculitis. Thus, further studies are warranted to investigate the role of IL-1 signaling not only in acute KD but also in the subsequent vascular remodeling and long-term complications of KD vasculitis, including accelerated atherosclerosis.
METHODS: Tamoxifen-inducible vascular smooth muscle cell-specific IL-1 receptor (Il1r1) knockout (SMCΔ/Δ) mice and Il1r1SMCWT/WT [wildtype/wildtype] littermate controls, all on ApoE-/- background, were injected with either PBS or Lactobacillus casei cell wall extract. Two weeks later, mice were fed a tamoxifen diet for 2 weeks to induce Il1r1 deletion on vascular smooth muscle cells before being exposed to 8 weeks of Western diet to promote atherosclerosis.
RESULTS: KD vasculitis led to a significant acceleration of atherosclerosis. Il1r1SMCΔ/Δ mice had significantly diminished atherosclerotic plaque size, macrophage infiltration, and necrotic core formation in the aortic root, as well as diminished lipid accumulation in the aorta en face compared with control mice, despite similar serum cholesterol levels. Il1r1SMCΔ/Δ mice also had significantly diminished expression of endothelial adhesion molecules VCAM-1 (vascular cell adhesion molecule 1) and ICAM-1 (intercellular adhesion molecule 1) in the lesion area, as well as reduced serum MCP-1 (monocyte chemotaxis protein-1) levels compared with Il1r1SMCWT/WT control mice. Monocyte and macrophage recruitment was significantly reduced in the Il1r1SMCΔ/Δ group compared with the Il1r1SMCWT/WT group.
CONCLUSIONS: Our results suggest an important pathophysiologic link between IL-1 signaling on vascular smooth muscle cells and subsequent acceleration of atherosclerosis in hypercholesterolemic mice following KD vasculitis. Thus, further studies are warranted to investigate the role of IL-1 signaling not only in acute KD but also in the subsequent vascular remodeling and long-term complications of KD vasculitis, including accelerated atherosclerosis.
Предметные рубрики MeSH
AnimalsMucocutaneous Lymph Node SyndromeAtherosclerosisDisease Models, AnimalMuscle, Smooth, VascularSignal TransductionMyocytes, Smooth MuscleMiceMice, KnockoutReceptors, Interleukin-1 Type IAortaInterleukin-1Plaque, AtheroscleroticMaleAortic DiseasesMice, Knockout, ApoEIntercellular Adhesion Molecule-1Lacticaseibacillus caseiMice, Inbred C57BL