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Can accelerated ageing models inform us on age-related tauopathies?

Zhuang Zhuang HanAlex FleetDelphine Larrieu
Published in: Aging cell (2023)
Ageing is the greatest risk factor of late-onset neurodegenerative diseases. In the realm of sporadic tauopathies, modelling the process of biological ageing in experimental animals forms the foundation of searching for the molecular origin of pathogenic tau and developing potential therapeutic interventions. Although prior research into transgenic tau models offers valuable lessons for studying how tau mutations and overexpression can drive tau pathologies, the underlying mechanisms by which ageing leads to abnormal tau accumulation remains poorly understood. Mutations associated with human progeroid syndromes have been proposed to be able to mimic an aged environment in animal models. Here, we summarise recent attempts in modelling ageing in relation to tauopathies using animal models that carry mutations associated with human progeroid syndromes, or genetic elements unrelated to human progeroid syndromes, or have exceptional natural lifespans, or a remarkable resistance to ageing-related disorders.
Keyphrases
  • late onset
  • endothelial cells
  • cerebrospinal fluid
  • induced pluripotent stem cells
  • pluripotent stem cells
  • early onset
  • risk factors
  • cell proliferation
  • physical activity
  • transcription factor
  • genome wide