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De novo lipogenesis fuels adipocyte autophagosome and lysosome membrane dynamics

Author

Listed:
  • Leslie A. Rowland

    (University of Massachusetts Chan Medical School)

  • Adilson Guilherme

    (University of Massachusetts Chan Medical School)

  • Felipe Henriques

    (University of Massachusetts Chan Medical School)

  • Chloe DiMarzio

    (University of Massachusetts Chan Medical School)

  • Sean Munroe

    (University of Massachusetts Chan Medical School)

  • Nicole Wetoska

    (University of Massachusetts Chan Medical School)

  • Mark Kelly

    (University of Massachusetts Chan Medical School)

  • Keith Reddig

    (University of Massachusetts Chan Medical School)

  • Gregory Hendricks

    (University of Massachusetts Chan Medical School)

  • Meixia Pan

    (University of Texas Health Science Center at San Antonio)

  • Xianlin Han

    (University of Texas Health Science Center at San Antonio
    University of Texas Health Science Center at San Antonio)

  • Olga R. Ilkayeva

    (Duke University School of Medicine)

  • Christopher B. Newgard

    (Duke University School of Medicine)

  • Michael P. Czech

    (University of Massachusetts Chan Medical School)

Abstract

Adipocytes robustly synthesize fatty acids (FA) from carbohydrate through the de novo lipogenesis (DNL) pathway, yet surprisingly DNL contributes little to their abundant triglyceride stored in lipid droplets. This conundrum raises the hypothesis that adipocyte DNL instead enables membrane expansions to occur in processes like autophagy, which requires an abundant supply of phospholipids. We report here that adipocyte Fasn deficiency in vitro and in vivo markedly impairs autophagy, evident by autophagosome accumulation and severely compromised degradation of the autophagic substrate p62. Our data indicate the impairment occurs at the level of autophagosome-lysosome fusion, and indeed, loss of Fasn decreases certain membrane phosphoinositides necessary for autophagosome and lysosome maturation and fusion. Autophagy dependence on FA produced by Fasn is not fully alleviated by exogenous FA in cultured adipocytes, and interestingly, imaging studies reveal that Fasn colocalizes with nascent autophagosomes. Together, our studies identify DNL as a critical source of FAs to fuel autophagosome and lysosome maturation and fusion in adipocytes.

Suggested Citation

  • Leslie A. Rowland & Adilson Guilherme & Felipe Henriques & Chloe DiMarzio & Sean Munroe & Nicole Wetoska & Mark Kelly & Keith Reddig & Gregory Hendricks & Meixia Pan & Xianlin Han & Olga R. Ilkayeva &, 2023. "De novo lipogenesis fuels adipocyte autophagosome and lysosome membrane dynamics," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37016-8
    DOI: 10.1038/s41467-023-37016-8
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    1. Mackenzie E. Smith & Chuck T. Chen & Chiraag A. Gohel & Giulia Cisbani & Daniel K. Chen & Kimia Rezaei & Andrew McCutcheon & Richard P. Bazinet, 2024. "Upregulated hepatic lipogenesis from dietary sugars in response to low palmitate feeding supplies brain palmitate," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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