| Autor: |
Naia, Luana, Shimozawa, Makoto, Bereczki, Erika, Li, Xidan, Liu, Jianping, Jiang, Richeng, Giraud, Romain, Leal, Nuno Santos, Pinho, Catarina Moreira, Berger, Erik, Falk, Victoria Lim, Dentoni, Giacomo, Ankarcrona, Maria, Nilsson, Per |
| Zdroj: |
Molecular Psychiatry; 20230101, Issue: Preprints p1-16, 16p |
| Abstrakt: |
Accumulation of amyloid β-peptide (Aβ) is a driver of Alzheimer’s disease (AD). Amyloid precursor protein (App) knock-in mouse models recapitulate AD-associated Aβ pathology, allowing elucidation of downstream effects of Aβ accumulation and their temporal appearance upon disease progression. Here we have investigated the sequential onset of AD-like pathologies in AppNL-Fand AppNL-G-Fknock-in mice by time-course transcriptome analysis of hippocampus, a region severely affected in AD. Strikingly, energy metabolism emerged as one of the most significantly altered pathways already at an early stage of pathology. Functional experiments in isolated mitochondria from hippocampus of both AppNL-Fand AppNL-G-Fmice confirmed an upregulation of oxidative phosphorylation driven by the activity of mitochondrial complexes I, IV and V, associated with higher susceptibility to oxidative damage and Ca2+-overload. Upon increasing pathologies, the brain shifts to a state of hypometabolism with reduced abundancy of mitochondria in presynaptic terminals. These late-stage mice also displayed enlarged presynaptic areas associated with abnormal accumulation of synaptic vesicles and autophagosomes, the latter ultimately leading to local autophagy impairment in the synapses. In summary, we report that Aβ-induced pathways in Appknock-in mouse models recapitulate key pathologies observed in AD brain, and our data herein adds a comprehensive understanding of the pathologies including dysregulated metabolism and synapses and their timewise appearance to find new therapeutic approaches for AD. |
| Databáze: |
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