Table of Contents

Modality-Specific Impairment of Hippocampal CA1 Neurons of Alzheimer’s Disease Model Mice

  1. Yasunori Hayashi1,4,5
  1. 1Department of Pharmacology, Kyoto University Graduate School of Medicine, Kyoto 606-8501, Japan
  2. 2Department of Life Science and Medical Bioscience, Graduate School of Advanced Science and Engineering, Waseda University, Tokyo 162-8480, Japan
  3. 3Center for Brain Science, RIKEN, Saitama 351-0198, Japan
  4. 4Brain Science Institute, RIKEN, Saitama 351-0198, Japan
  5. 5Brain and Body System Science Institute, Saitama University, Saitama 338-8570, Japan
  1. Author contributions: K.M. and Y.H. designed research; R.T., K.M., and Y.S. performed research; T.S., M.O., J.N., and T.C.S. contributed unpublished reagents/analytic tools; R.T., K.M., T.I., and M.S. analyzed data; and R.T., K.M., T.O., and Y.H. wrote the paper.

Abstract

Impairment of episodic memory, a class of memory for spatiotemporal context of an event, is an early symptom of Alzheimer’s disease. Both spatial and temporal information are encoded and represented in the hippocampal neurons, but how these representations are impaired under amyloid β (Aβ) pathology remains elusive. We performed chronic imaging of the hippocampus in awake male amyloid precursor protein (App) knock-in mice behaving in a virtual reality environment to simultaneously monitor spatiotemporal representations and the progression of Aβ depositions. We found that temporal representation is preserved, whereas spatial representation is significantly impaired in the App knock-in mice. This is because of the overall reduction of active place cells, but not time cells, and compensatory hyperactivation of remaining place cells near Aβ aggregates. These results indicate the differential impact of Aβ aggregates on two major modalities of episodic memory, suggesting different mechanisms for forming and maintaining these two representations in the hippocampus.

  • Received January 28, 2021.
  • Revision received April 10, 2021.
  • Accepted April 23, 2021.