Intraneuronal accumulation of C99 contributes to synaptic alterations- apathy-like behavior- and spatial learning deficits in 3xTgAD and 2xTgAD mice

Authors
A Bourgeois, I Lauritzen, T Lorivel, C Bauer, F Checler, R Pardossi-Piquard

Lab
Université Côte d’Azur, INSERM, CNRS, IPMC, UMR7275, Sophia-Antipolis, Valbonne, France

Journal
Neurobiology of Aging

Abstract
The triple transgenic mouse model (3_TgAD: APPswe, TauP301L, PS1M146V) recapitulates both amyloid _ (Abeta)- and tau-related lesions as well as synaptic and memory deficits. In these mice, we reported an early apathy-like behavior and alterations in synaptic plasticity appearing concomitantly with intraneuronal accumulation of C99 in the subiculum. To delineate the genuine contribution of C99 on the above phenotypes, we generated double transgenic mice (2_TgAD: APPswe, TauP301L) that accumulate C99 without Abeta deposition or hyperphosphorylation of tau and compared them to 3_TgAD mice. Here, we show that both TgAD mice display similar decreases in long-term potentiation and in spontaneous locomotor activity measured by actimetry suggesting that the synaptic alterations and the apathy-like behavior were likely linked to C99 rather than Abeta. However, spatial learning alterations, assessed by the Morris water maze task, are more pronounced in 3_TgAD than in 2_TgAD, suggesting that both Abeta and C99 contribute to defects in the acquisition of spatial information. Finally, even if similar results are observed in males, cognitive and non-cognitive deficits are more severe in females.

BIOSEB Instruments Used:
Aron Test or Four Plates Test (LE830),Rotarod (BX-ROD)