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Thermogenic adipocytes promote HDL turnover and reverse cholesterol transport

Author

Listed:
  • Alexander Bartelt

    (University Medical Center Hamburg-Eppendorf
    University Medical Center Hamburg-Eppendorf
    Harvard T.H. Chan School of Public Health)

  • Clara John

    (University Medical Center Hamburg-Eppendorf)

  • Nicola Schaltenberg

    (University Medical Center Hamburg-Eppendorf)

  • Jimmy F. P. Berbée

    (Leiden University Medical Center)

  • Anna Worthmann

    (University Medical Center Hamburg-Eppendorf)

  • M. Lisa Cherradi

    (University Medical Center Hamburg-Eppendorf)

  • Christian Schlein

    (University Medical Center Hamburg-Eppendorf)

  • Julia Piepenburg

    (University Medical Center Hamburg-Eppendorf)

  • Mariëtte R. Boon

    (Leiden University Medical Center)

  • Franz Rinninger

    (University Medical Center Hamburg-Eppendorf)

  • Markus Heine

    (University Medical Center Hamburg-Eppendorf)

  • Klaus Toedter

    (University Medical Center Hamburg-Eppendorf)

  • Andreas Niemeier

    (University Medical Center Hamburg-Eppendorf)

  • Stefan K. Nilsson

    (University Medical Center Hamburg-Eppendorf
    Umeå University)

  • Markus Fischer

    (Hamburg School of Food Science, Institute of Food Chemistry, University of Hamburg)

  • Sander L. Wijers

    (NUTRIM - School for Nutrition, Toxicology and Metabolism, Maastricht University Medical Center)

  • Wouter van Marken Lichtenbelt

    (NUTRIM - School for Nutrition, Toxicology and Metabolism, Maastricht University Medical Center)

  • Ludger Scheja

    (University Medical Center Hamburg-Eppendorf)

  • Patrick C. N. Rensen

    (Leiden University Medical Center)

  • Joerg Heeren

    (University Medical Center Hamburg-Eppendorf)

Abstract

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.

Suggested Citation

  • 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, 2017. "Thermogenic adipocytes promote HDL turnover and reverse cholesterol transport," Nature Communications, Nature, vol. 8(1), pages 1-10, April.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15010
    DOI: 10.1038/ncomms15010
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    Cited by:

    1. Kang Chen & Lai Yee Cheong & Yuan Gao & Yaming Zhang & Tianshi Feng & Qin Wang & Leigang Jin & Eric Honoré & Karen S. L. Lam & Weiping Wang & Xiaoyan Hui & Aimin Xu, 2022. "Adipose-targeted triiodothyronine therapy counteracts obesity-related metabolic complications and atherosclerosis with negligible side effects," Nature Communications, Nature, vol. 13(1), pages 1-20, December.

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