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Methylene blue accelerates liquid-to-gel transition of tau condensates impacting tau function and pathology

Author

Listed:
  • Yongqi Huang

    (Hubei University of Technology)

  • Jitao Wen

    (Chinese Academy of Sciences
    University of the Chinese Academy of Sciences)

  • Lisa-Marie Ramirez

    (German Center for Neurodegenerative Diseases (DZNE))

  • Eymen Gümüşdil

    (German Center for Neurodegenerative Diseases (DZNE)
    Gebze Technical University)

  • Pravin Pokhrel

    (Kent State University)

  • Viet H. Man

    (University of Pittsburgh)

  • Haiqiong Ye

    (Hubei University of Technology)

  • Yue Han

    (Hubei University of Technology)

  • Yunfei Liu

    (Hubei University of Technology)

  • Ping Li

    (Hubei University of Technology)

  • Zhengding Su

    (Hubei University of Technology)

  • Junmei Wang

    (University of Pittsburgh)

  • Hanbin Mao

    (Kent State University)

  • Markus Zweckstetter

    (German Center for Neurodegenerative Diseases (DZNE)
    Max Planck Institute for Multidisciplinary Sciences)

  • Sarah Perrett

    (Chinese Academy of Sciences
    University of the Chinese Academy of Sciences)

  • Si Wu

    (Chinese Academy of Sciences
    University of the Chinese Academy of Sciences)

  • Meng Gao

    (Hubei University of Technology)

Abstract

Preventing tau aggregation is a potential therapeutic strategy in Alzheimer’s disease and other tauopathies. Recently, liquid–liquid phase separation has been found to facilitate the formation of pathogenic tau conformations and fibrillar aggregates, although many aspects of the conformational transitions of tau during the phase transition process remain unknown. Here, we demonstrate that the tau aggregation inhibitor methylene blue promotes tau liquid–liquid phase separation and accelerates the liquid-to-gel transition of tau droplets independent of the redox activity of methylene blue. We further show that methylene blue inhibits the conversion of tau droplets into fibrils and reduces the cytotoxicity of tau aggregates. Although gelation slows down the mobility of tau and tubulin, it does not impair microtubule assembly within tau droplets. These findings suggest that methylene blue inhibits tau amyloid fibrillization and accelerates tau droplet gelation via distinct mechanisms, thus providing insights into the activity of tau aggregation inhibitors in the context of phase transition.

Suggested Citation

  • Yongqi Huang & Jitao Wen & Lisa-Marie Ramirez & Eymen Gümüşdil & Pravin Pokhrel & Viet H. Man & Haiqiong Ye & Yue Han & Yunfei Liu & Ping Li & Zhengding Su & Junmei Wang & Hanbin Mao & Markus Zweckste, 2023. "Methylene blue accelerates liquid-to-gel transition of tau condensates impacting tau function and pathology," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41241-6
    DOI: 10.1038/s41467-023-41241-6
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    References listed on IDEAS

    as
    1. Pablo Gracia & David Polanco & Jorge Tarancón-Díez & Ilenia Serra & Maruan Bracci & Javier Oroz & Douglas V. Laurents & Inés García & Nunilo Cremades, 2022. "Molecular mechanism for the synchronized electrostatic coacervation and co-aggregation of alpha-synuclein and tau," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Nicholas M. Kanaan & Chelsey Hamel & Tessa Grabinski & Benjamin Combs, 2020. "Liquid-liquid phase separation induces pathogenic tau conformations in vitro," Nature Communications, Nature, vol. 11(1), pages 1-16, December.
    3. Susmitha Ambadipudi & Jacek Biernat & Dietmar Riedel & Eckhard Mandelkow & Markus Zweckstetter, 2017. "Liquid–liquid phase separation of the microtubule-binding repeats of the Alzheimer-related protein Tau," Nature Communications, Nature, vol. 8(1), pages 1-13, December.
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