Early intermittent hyperlipidaemia alters tissue macrophages to fuel atherosclerosis
成果类型:
Article
署名作者:
Takaoka, Minoru; Zhao, Xiaohui; Lim, Hwee Ying; Magnussen, Costan G.; Ang, Owen; Suffee, Nadine; Schrank, Patricia R.; Ong, Wei Siong; Tsiantoulas, Dimitrios; Sommer, Felix; Mohanta, Sarajo K.; Harrison, James; Meng, Yaxing; Laurans, Ludivine; Wu, Feitong; Lu, Yuning; Masters, Leanne; Newland, Stephen A.; Denti, Laura; Hong, Mingyang; Chajadine, Mouna; Juonala, Markus; Koskinen, Juhani S.; Kaehoenen, Mika; Pahkala, Katja; Rovio, Suvi P.; Mykkaenen, Juha; Thomson, Russell; Kaisho, Tsuneyasu; Habenicht, Andreas J. R.; Clement, Marc; Tedgui, Alain; Ait-Oufella, Hafid; Zhao, Tian X.; Nus, Meritxell; Ruhrberg, Christiana; Taleb, Soraya; Williams, Jesse W.; Raitakari, Olli T.; Angeli, Veronique; Mallat, Ziad
署名单位:
University of Cambridge; National University of Singapore; National University of Singapore; University of Turku; University of Turku; University of Turku; Baker Heart and Diabetes Institute; Universite Paris Cite; Institut National de la Sante et de la Recherche Medicale (Inserm); University of Minnesota System; University of Minnesota Twin Cities; Medical University of Vienna; University of Kiel; University of Kiel; Schleswig Holstein University Hospital; University of Munich; University of London; University College London; University of Turku; University of Turku; Satakunta Central Hospital; Tampere University; Tampere University; Tampere University; Wakayama Medical University; University of Turku
刊物名称:
Nature
ISSN/ISSBN:
0028-5888
DOI:
10.1038/s41586-024-07993-x
发表日期:
2024-10-10
关键词:
myocardial-infarction
cholesterol variability
cardiovascular risk
enrichment analysis
web server
gene
associations
activation
childhood
deficient
摘要:
Hyperlipidaemia is a major risk factor of atherosclerotic cardiovascular disease (ASCVD). Risk of cardiovascular events depends on cumulative lifetime exposure to low-density lipoprotein cholesterol (LDL-C) and, independently, on the time course of exposure to LDL-C, with early exposure being associated with a higher risk1. Furthermore, LDL-C fluctuations are associated with ASCVD outcomes2-4. However, the precise mechanisms behind this increased ASCVD risk are not understood. Here we find that early intermittent feeding of mice on a high-cholesterol Western-type diet (WD) accelerates atherosclerosis compared with late continuous exposure to the WD, despite similar cumulative circulating LDL-C levels. We find that early intermittent hyperlipidaemia alters the number and homeostatic phenotype of resident-like arterial macrophages. Macrophage genes with altered expression are enriched for genes linked to human ASCVD in genome-wide association studies. We show that LYVE1+ resident macrophages are atheroprotective, and identify biological pathways related to actin filament organization, of which alteration accelerates atherosclerosis. Using the Young Finns Study, we show that exposure to cholesterol early in life is significantly associated with the incidence and size of carotid atherosclerotic plaques in mid-adulthood. In summary, our results identify early intermittent exposure to cholesterol as a strong determinant of accelerated atherosclerosis, highlighting the importance of optimal control of hyperlipidaemia early in life, and providing insights into the underlying biological mechanisms. This knowledge will be essential to designing effective therapeutic strategies to combat ASCVD. Early intermittent feeding of mice with a high-cholesterol Western-type diet accelerates atherosclerosis compared with late continuous exposure to the Western-type diet, despite similar cumulative circulating LDL-C levels.