内科学
内分泌学
产热
胆固醇逆向转运
胆固醇
清道夫受体
脂解
刺激
化学
脂肪组织
脂肪细胞
脂蛋白
生物
医学
作者
Alexander Bartelt,Clara John,Nicola Schaltenberg,Jimmy F.P. Berbée,Anna Worthmann,M. Lisa Cherradi,Christian Schlein,Julia Piepenburg,Mariëtte R. Boon,Franz Rinninger,Markus Heine,K. Toedter,Andreas Niemeier,Stefan K. Nilsson,Markus Fischer,S. Wijers,Wouter van Marken Lichtenbelt,Ludger Scheja,Patrick C.N. Rensen,Jöerg Heeren
摘要
Brown and beige adipocytes combust nutrients for thermogenesis and through their metabolic activity decrease pro-atherogenic remnant lipoproteins in hyperlipidemic mice. However, whether the activation of thermogenic adipocytes affects the metabolism and anti-atherogenic properties of high-density lipoproteins (HDL) is unknown. Here, we report a reduction in atherosclerosis in response to pharmacological stimulation of thermogenesis linked to increased HDL levels in APOE*3-Leiden.CETP mice. Both cold-induced and pharmacological thermogenic activation enhances HDL remodelling, which is associated with specific lipidomic changes in mouse and human HDL. Furthermore, thermogenic stimulation promotes HDL-cholesterol clearance and increases macrophage-to-faeces reverse cholesterol transport in mice. Mechanistically, we show that intravascular lipolysis by adipocyte lipoprotein lipase and hepatic uptake of HDL by scavenger receptor B-I are the driving forces of HDL-cholesterol disposal in liver. Our findings corroborate the notion that high metabolic activity of thermogenic adipocytes confers atheroprotective properties via increased systemic cholesterol flux through the HDL compartment.
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