The role of postnatal neurogenesis in supporting remote memory and spatial metric processing

Hippocampus. 2014 Dec;24(12):1663-71. doi: 10.1002/hipo.22346. Epub 2014 Aug 27.

Abstract

In this study, we determined the contribution of juvenile neurogenesis to the performance of mice on a remote memory for temporally based association task and in a novelty based spatial pattern separation task. This was accomplished by mating homozygous DNMT1-loxP mice with heterozygous GFAP-Cre mice and comparing Cre+ (no postnatal neurogenesis) to Cre- (wild type) littermate offspring. The results indicate that Cre+ mice are impaired relative to Cre- mice in the remote memory for a temporal based association task and in a novelty based spatial pattern separation task. These results support the temporal integration model of Aimone et al., [(2006) Nat Neurosci 9:723-727] and provide further support for an important role for postnatally born neurons in spatial pattern separation. In contrast, Cre+ mice are not impaired relative to Cre- mice in an object-context recognition task and a spatial location recognition task. These latter data suggest that postnatally derived neurons in the dentate gyrus (DG) do not support all spatial and object recognition functions of the DG.

Keywords: 1-c knockout mice; DNA methyltransferase; cued recall task; object recognition; pattern separation; spatial recognition.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Association Learning / physiology*
  • Bromodeoxyuridine
  • Cues
  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNA (Cytosine-5-)-Methyltransferases / genetics
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • Dentate Gyrus / physiology
  • Male
  • Memory, Long-Term / physiology*
  • Mental Recall / physiology
  • Mice, Knockout
  • Neurogenesis / physiology*
  • Neurons / physiology
  • Neuropsychological Tests
  • Recognition, Psychology / physiology
  • Space Perception / physiology*

Substances

  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNA (Cytosine-5-)-Methyltransferases
  • Dnmt1 protein, mouse
  • Bromodeoxyuridine