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Thermogenic adipocytes promote HDL turnover and reverse cholesterol transport

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 l...

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Detalles Bibliográficos
Autores principales: Bartelt, Alexander, John, Clara, Schaltenberg, Nicola, Berbée, Jimmy F. P., Worthmann, Anna, Cherradi, M. Lisa, Schlein, Christian, Piepenburg, Julia, Boon, Mariëtte R., Rinninger, Franz, Heine, Markus, Toedter, Klaus, Niemeier, Andreas, Nilsson, Stefan K., Fischer, Markus, Wijers, Sander L., van Marken Lichtenbelt, Wouter, Scheja, Ludger, Rensen, Patrick C. N., Heeren, Joerg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399294/
https://www.ncbi.nlm.nih.gov/pubmed/28422089
http://dx.doi.org/10.1038/ncomms15010
Descripción
Sumario: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.