Impaired Memory in OT-II Transgenic Mice Is Associated with Decreased Adult Hippocampal Neurogenesis Possibly Induced by Alteration in Th2 Cytokine Levels

Mol Cells. 2016 Aug 31;39(8):603-10. doi: 10.14348/molcells.2016.0072. Epub 2016 Jul 19.

Abstract

Recently, an increasing number of studies have focused on the effects of CD4+ T cell on cognitive function. However, the changes of Th2 cytokines in restricted CD4+ T cell receptor (TCR) repertoire model and their effects on the adult hippocampal neurogenesis and memory are not fully understood. Here, we investigated whether and how the mice with restricted CD4+ repertoire TCR exhibit learning and memory impairment by using OT-II mice. OT-II mice showed decreased adult neurogenesis in hippocampus and short- and long- term memory impairment. Moreover, Th2 cytokines in OT-II mice are significantly increased in peripheral organs and IL-4 is significantly increased in brain. Finally, IL-4 treatment significantly inhibited the proliferation of cultured adult rat hippocampal neural stem cells. Taken together, abnormal level of Th2 cytokines can lead memory dysfunction via impaired adult neurogenesis in OT-II transgenic.

Keywords: CD4 T cells; OT-II transgenic mice; Th2 cytokines; adult neurogenesis; cognition.

MeSH terms

  • Animals
  • Cell Proliferation
  • Cells, Cultured
  • Cognition* / physiology
  • Hippocampus / metabolism*
  • Hippocampus / pathology
  • Interleukin-4 / metabolism*
  • Male
  • Memory Disorders / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neural Stem Cells / physiology*
  • Neurogenesis* / genetics
  • Neurogenesis* / immunology
  • Neuroimmunomodulation
  • Rats
  • Rats, Inbred Strains
  • Receptors, Antigen, T-Cell / genetics
  • Th2 Cells / physiology*

Substances

  • Receptors, Antigen, T-Cell
  • Interleukin-4