Liver X receptor β regulates the development of the dentate gyrus and autistic-like behavior in the mouse

Proc Natl Acad Sci U S A. 2018 Mar 20;115(12):E2725-E2733. doi: 10.1073/pnas.1800184115. Epub 2018 Mar 5.

Abstract

The dentate gyrus (DG) of the hippocampus is a laminated brain region in which neurogenesis begins during early embryonic development and continues until adulthood. Recent studies have implicated that defects in the neurogenesis of the DG seem to be involved in the genesis of autism spectrum disorders (ASD)-like behaviors. Liver X receptor β (LXRβ) has recently emerged as an important transcription factor involved in the development of laminated CNS structures, but little is known about its role in the development of the DG. Here, we show that deletion of the LXRβ in mice causes hypoplasia in the DG, including abnormalities in the formation of progenitor cells and granule cell differentiation. We also found that expression of Notch1, a central mediator of progenitor cell self-renewal, is reduced in LXRβ-null mice. In addition, LXRβ deletion in mice results in autistic-like behaviors, including abnormal social interaction and repetitive behavior. These data reveal a central role for LXRβ in orchestrating the timely differentiation of neural progenitor cells within the DG, thereby providing a likely explanation for its association with the genesis of autism-related behaviors in LXRβ-deficient mice.

Keywords: LXRβ; autism; dentate gyrus; development; progenitor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autistic Disorder / etiology*
  • Autistic Disorder / genetics
  • Behavior, Animal / physiology
  • Cell Differentiation
  • Cell Proliferation / genetics
  • Dentate Gyrus / cytology
  • Dentate Gyrus / growth & development*
  • Dentate Gyrus / metabolism
  • Fatty Acid-Binding Protein 7 / metabolism
  • Female
  • Gene Expression Regulation, Developmental
  • Liver X Receptors / genetics
  • Liver X Receptors / metabolism*
  • Male
  • Mice, Knockout
  • Neuroglia / cytology
  • Neurons / pathology*
  • Neurons / physiology
  • Receptor, Notch1 / metabolism
  • Stem Cells / cytology
  • Stem Cells / physiology

Substances

  • Fabp7 protein, mouse
  • Fatty Acid-Binding Protein 7
  • Liver X Receptors
  • Notch1 protein, mouse
  • Receptor, Notch1