Long-term Memory Upscales Volume of Postsynaptic Densities in the Process that Requires Autophosphorylation of αCaMKII

Author:

Śliwińska Małgorzata Alicja12,Cały Anna1,Borczyk Malgorzata1,Ziółkowska Magdalena1,Skonieczna Edyta1,Chilimoniuk Magdalena1,Bernaś Tytus23,Giese K Peter4,Radwanska Kasia1

Affiliation:

1. Laboratory of Molecular Basis of Behavior, The Nencki Institute of Experimental Biology of Polish Academy of Sciences, Warsaw 02-093, Poland

2. Laboratory of Imaging Tissue Structure and Function, The Nencki Institute of Experimental Biology of Polish Academy of Sciences, Warsaw 02-093, Poland

3. Department of Anatomy and Neurology, VCU School of Medicine, Richmond, VA 23298, USA

4. Department of Basic and Clinical Neuroscience, King's College London, 125 Coldharbour Lane, London SE5 9NU, UK

Abstract

Abstract It is generally accepted that formation and storage of memory relies on alterations of the structure and function of brain circuits. However, the structural data, which show learning-induced and long-lasting remodeling of synapses, are still very sparse. Here, we reconstruct 1927 dendritic spines and their postsynaptic densities (PSDs), representing a postsynaptic part of the glutamatergic synapse, in the hippocampal area CA1 of the mice that underwent spatial training. We observe that in young adult (5 months), mice volume of PSDs, but not the volume of the spines, is increased 26 h after the training. The training-induced growth of PSDs is specific for the dendritic spines that lack smooth endoplasmic reticulum and spine apparatuses, and requires autophosphorylation of αCaMKII. Interestingly, aging alters training-induced ultrastructural remodeling of dendritic spines. In old mice, both the median volumes of dendritic spines and PSDs shift after training toward bigger values. Overall, our data support the hypothesis that formation of memory leaves long-lasting footprint on the ultrastructure of brain circuits; however, the form of circuit remodeling changes with age.

Funder

National Science Centre

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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