Disrupted Place Cell Remapping and Impaired Grid Cells in a Knockin Model of Alzheimer's Disease

Neuron. 2020 Sep 23;107(6):1095-1112.e6. doi: 10.1016/j.neuron.2020.06.023. Epub 2020 Jul 21.

Abstract

Patients with Alzheimer's disease (AD) suffer from spatial memory impairment and wandering behavior, but the brain circuit mechanisms causing such symptoms remain largely unclear. In healthy brains, spatially tuned hippocampal place cells and entorhinal grid cells exhibit distinct spike patterns in different environments, a circuit function called "remapping." We tested remapping in amyloid precursor protein knockin (APP-KI) mice with impaired spatial memory. CA1 neurons, including place cells, showed disrupted remapping, although their spatial tuning was only mildly diminished. Medial entorhinal cortex (MEC) neurons severely lost their spatial tuning and grid cells were almost absent. Fast gamma oscillatory coupling between the MEC and CA1 was also impaired. Mild disruption of MEC grid cells emerged in younger APP-KI mice, although the spatial memory and CA1 remapping of the animals remained intact. These results point to remapping impairment in the hippocampus, possibly linked to grid cell disruption, as circuit mechanisms underlying spatial memory impairment in AD.

Keywords: Alzheimer's disease; amyloid precursor protein; gamma oscillations; grid cells; knockin; place cells; remapping.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / genetics
  • Alzheimer Disease / pathology
  • Alzheimer Disease / physiopathology*
  • Amyloid beta-Protein Precursor / genetics
  • Animals
  • CA1 Region, Hippocampal / pathology
  • CA1 Region, Hippocampal / physiopathology*
  • Connectome*
  • Entorhinal Cortex / pathology
  • Entorhinal Cortex / physiopathology*
  • Female
  • Gamma Rhythm
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neural Pathways / pathology
  • Neural Pathways / physiopathology
  • Neurons / classification*
  • Neurons / pathology
  • Neurons / physiology

Substances

  • APP protein, mouse
  • Amyloid beta-Protein Precursor