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Modeling Alzheimer's disease related phenotypes in the Ts65Dn mouse: impact of age on Aß, Tau, pTau, NfL, and behavior.
Overk, Cassia; Fiorini, Emma; Babolin, Chiara; Vukicevic, Marija; Morici, Catherine; Madani, Rime; Eligert, Valerie; Kosco-Vilbois, Marie; Roberts, Amanda; Becker, Ann; Pfeifer, Andrea; Mobley, William C.
Afiliación
  • Overk C; Department of Neurosciences, University of California, San Diego, La Jolla, CA, United States.
  • Fiorini E; AC Immune SA, Lausanne, Switzerland.
  • Babolin C; AC Immune SA, Lausanne, Switzerland.
  • Vukicevic M; AC Immune SA, Lausanne, Switzerland.
  • Morici C; AC Immune SA, Lausanne, Switzerland.
  • Madani R; AC Immune SA, Lausanne, Switzerland.
  • Eligert V; AC Immune SA, Lausanne, Switzerland.
  • Kosco-Vilbois M; AC Immune SA, Lausanne, Switzerland.
  • Roberts A; Animal Models Core Facility, The Scripps Research Institute, La Jolla, CA, United States.
  • Becker A; Department of Neurosciences, University of California, San Diego, La Jolla, CA, United States.
  • Pfeifer A; AC Immune SA, Lausanne, Switzerland.
  • Mobley WC; Department of Neurosciences, University of California, San Diego, La Jolla, CA, United States.
Front Neurosci ; 17: 1202208, 2023.
Article en En | MEDLINE | ID: mdl-37449271
ABSTRACT

Introduction:

People with DS are highly predisposed to Alzheimer's disease (AD) and demonstrate very similar clinical and pathological features. Ts65Dn mice are widely used and serve as the best-characterized animal model of DS.

Methods:

We undertook studies to characterize age-related changes for AD-relevant markers linked to Aß, Tau, and phospho-Tau, axonal structure, inflammation, and behavior.

Results:

We found age related changes in both Ts65Dn and 2N mice. Relative to 2N mice, Ts65Dn mice showed consistent increases in Aß40, insoluble phospho-Tau, and neurofilament light protein. These changes were correlated with deficits in learning and memory.

Discussion:

These data have implications for planning future experiments aimed at preventing disease-related phenotypes and biomarkers. Interventions should be planned to address specific manifestations using treatments and treatment durations adequate to engage targets to prevent the emergence of phenotypes.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurosci Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos