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Human beige adipocytes for drug discovery and cell therapy in metabolic diseases

Author

Listed:
  • Amar M. Singh

    (University of Georgia)

  • Liang Zhang

    (University of Georgia)

  • John Avery

    (University of Georgia)

  • Amelia Yin

    (University of Georgia)

  • Yuhong Du

    (Emory University School of Medicine)

  • Hui Wang

    (University of North Carolina Chapel Hill)

  • Zibo Li

    (University of North Carolina Chapel Hill)

  • Haian Fu

    (Emory University School of Medicine
    Emory University School of Medicine)

  • Hang Yin

    (University of Georgia)

  • Stephen Dalton

    (University of Georgia)

Abstract

Human beige adipocytes (BAs) have potential utility for the development of therapeutics to treat diabetes and obesity-associated diseases. Although several reports have described the generation of beige adipocytes in vitro, their potential utility in cell therapy and drug discovery has not been reported. Here, we describe the generation of BAs from human adipose-derived stem/stromal cells (ADSCs) in serum-free medium with efficiencies >90%. Molecular profiling of beige adipocytes shows them to be similar to primary BAs isolated from human tissue. In vitro, beige adipocytes exhibit uncoupled mitochondrial respiration and cAMP-induced lipolytic activity. Following transplantation, BAs increase whole-body energy expenditure and oxygen consumption, while reducing body-weight in recipient mice. Finally, we show the therapeutic utility of BAs in a platform for high-throughput drug screening (HTS). These findings demonstrate the potential utility of BAs as a cell therapeutic and as a tool for the identification of drugs to treat metabolic diseases.

Suggested Citation

  • Amar M. Singh & Liang Zhang & John Avery & Amelia Yin & Yuhong Du & Hui Wang & Zibo Li & Haian Fu & Hang Yin & Stephen Dalton, 2020. "Human beige adipocytes for drug discovery and cell therapy in metabolic diseases," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16340-3
    DOI: 10.1038/s41467-020-16340-3
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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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