交易激励
炎症
过氧化物酶体增殖物激活受体
内科学
内分泌学
转换抑制
PPAR激动剂
肝细胞
血脂异常
低密度脂蛋白受体
受体
医学
脂蛋白
药理学
化学
胆固醇
体外
糖尿病
生物化学
转录因子
基因
作者
Doriane Henry,Eric Baugé,Nathalie Hennuyer,Kévin Ory,Bruno Derudas,Emmanuelle Vallez,Audrey Deprince,Philippe Lefèbvre,Joel T. Haas,Bart Staels,Fanny Lalloyer
标识
DOI:10.1126/scitranslmed.adj8192
摘要
. Mechanistically, ligand-activated hepatocyte-specific transrepressive PPARα activity decreased the pro-inflammatory phenotype of hepatocytes, lowered the recruitment of leukocytes in the liver, reduced plasma IL-1β concentrations, and decreased atherosclerotic plaque macrophage content. These findings identify a distal effect of hepatic PPARα on vascular integrity rather linked to its anti-inflammatory activity than its lipid-lowering actions and highlight an essential role of targeting inflammation in CVD.
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