JNK Activation Correlates with Cognitive Impairment and Alteration of the Post-Synaptic Element in the 5xFAD AD Mouse Model
Open Access
Abstract
The c-Jun N-terminal kinases (JNKs) are a family of proteins that, once activated by stress stimuli, can alter neuronal functions and survival. The JNK cascade plays a crucial role in the post-synaptic neuronal compartment by altering its structural organization and leading, at worst, to an overall impairment of neuronal communication. Increasing evidence suggests that synaptic impairment is the first neurodegenerative event in Alzheimer’s disease (AD). To better elucidate this mechanism, we longitudinally studied 5xFAD mice at three selected time points representative of human AD symptom progression. We tested the mice cognitive performance by using the radial arm water maze (RAWM) in parallel with biochemical evaluations of post-synaptic enriched protein fraction and total cortical parenchyma. We found that 5xFAD mice presented a strong JNK activation at 3.5 months of age in the post-synaptic enriched protein fraction. This JNK activation correlates with a structural alteration of the post-synaptic density area and with memory impairment at this early stage of the disease that progressively declines to cause cell death. These findings pave the way for future studies on JNK as a key player in early neurodegeneration and as an important therapeutic target for the development of new compounds able to tackle synaptic impairment in the early phase of AD pathology.Keywords
Funding Information
- Ricerca Finalizzata (RF-2016-02361941, 847749, 2017MYJ5TH, BB/S00324X/1, AIS2110\33)
- European Commission’s Horizon 2020 Research and Innovation Program (RF-2016-02361941, 847749, 2017MYJ5TH, BB/S00324X/1, AIS2110\33)
- MIUR Bando PRIN 2017 (RF-2016-02361941, 847749, 2017MYJ5TH, BB/S00324X/1, AIS2110\33)
- Biotechnology and Biological Sciences Research Council (RF-2016-02361941, 847749, 2017MYJ5TH, BB/S00324X/1, AIS2110\33)
- Dunhill Medical Trust (RF-2016-02361941, 847749, 2017MYJ5TH, BB/S00324X/1, AIS2110\33)
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