RT Journal Article
SR Electronic
T1 PSD-95 in CA1 area regulates spatial choice depending on age
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP JN-RM-1996-20
DO 10.1523/JNEUROSCI.1996-20.2020
A1 Cały, Anna
A1 Śliwińska, Małgorzata A.
A1 Ziółkowska, Magdalena
A1 Łukasiewicz, Kacper
A1 Pagano, Roberto
A1 Dzik, Jakub M.
A1 Kalita, Katarzyna
A1 Bernaś, Tytus
A1 Stewart, Michael G.
A1 Giese, K. Peter
A1 Radwanska, Kasia
YR 2021
UL http://www.jneurosci.org/content/early/2021/01/14/JNEUROSCI.1996-20.2020.abstract
AB Cognitive processes that require spatial information rely on synaptic plasticity in the dorsal CA1 area (dCA1) of the hippocampus. Since the function of the hippocampus is impaired in aged individuals, it remains unknown how aged animals make spatial choices. Here, we used IntelliCage to study behavioural processes that support spatial choices of aged female mice living in a group. As a proxy of training-induced synaptic plasticity, we analysed the morphology of dendritic spines and expression of a synaptic scaffold protein, PSD-95. We observed that spatial choice training in young adult mice induced correlated shrinkage of dendritic spines and downregulation of PSD-95 in dCA1. Moreover, long-term depletion of PSD-95 by shRNA in dCA1 limited correct choices to a reward corner, while reward preference was intact. In contrast, old mice used behavioural strategies characterised by an increased tendency for perseverative visits and social interactions. This strategy resulted in a robust preference for the reward corner during the spatial choice task. Moreover, training decreased the correlation between PSD-95 expression and the size of dendritic spines. Furthermore, PSD-95 depletion did not impair place choice or reward preference in old mice. Thus, our data indicate that while young mice require PSD-95-dependent synaptic plasticity in dCA1 to make correct spatial choices, old animals observe cage-mates and stick to a preferred corner to seek the reward. This strategy is resistant to the depletion of PSD-95 in the CA1 area. Overall, our study demonstrates that aged mice combine alternative behavioral and molecular strategies to approach and consume rewards in a complex environment.SIGNIFICANCE STATEMENT: It remains poorly understood how ageing affects behavioural and molecular processes that support cognitive functions. It is, however, essential to understand these processes in order to develop therapeutic interventions that support successful cognitive ageing. Our data indicate that while young mice require PSD-95-dependent synaptic plasticity in dCA1 to make correct spatial choices (i.e. choices that require spatial information), old animals observe cage-mates and stick to a preferred corner to seek the reward. This strategy is resistant to the depletion of PSD-95 in the CA1 area. Overall, our study demonstrates that aged mice combine alternative behavioral and molecular strategies to approach and consume rewards in a complex environment. Secondly, the contribution of PSD-95-dependent synaptic functions in spatial choice changes with age.