TLX is an intrinsic regulator of the negative effects of IL-1β on proliferating hippocampal neural progenitor cells

FASEB J. 2018 Feb;32(2):613-624. doi: 10.1096/fj.201700495R. Epub 2018 Jan 4.

Abstract

Hippocampal neurogenesis is a lifelong process whereby new neurons are produced and integrate into the host circuitry within the hippocampus. It is regulated by a multitude of extrinsic and intrinsic regulators and is believed to contribute to certain hippocampal-dependent cognitive tasks. Hippocampal neurogenesis and associated cognition have been demonstrated to be impaired after increases in the levels of proinflammatory cytokine IL-1β in the hippocampus, such as that which occurs in various neurodegenerative and psychiatric disorders. IL-1β also suppresses the expression of TLX (orphan nuclear receptor tailless homolog), which is an orphan nuclear receptor that functions to promote neural progenitor cell (NPC) proliferation and suppress neuronal differentiation; therefore, manipulation of TLX represents a potential strategy with which to prevent the antiproliferative effects of IL-1β. In this study, we assessed the mechanism that underlies IL-1β-induced changes in TLX expression and determined the protective capacity of TLX to mitigate the effects of IL-1β on embryonic rat hippocampal neurosphere expansion. We demonstrate that IL-1β activated the NF-κB pathway in proliferating NPCs and that this activation was responsible for IL-1β-induced changes in TLX expression. In addition, we report that enhancing TLX expression prevented the IL-1β-induced suppression of neurosphere expansion. Thus, we highlight TLX as a potential protective regulator of the antiproliferative effects of IL-1β on hippocampal neurogenesis.-Ó'Léime, C. S., Kozareva, D. A., Hoban, A. E., Long-Smith, C. M., Cryan, J. F., Nolan, Y. M. TLX is an intrinsic regulator of the negative effects of IL-1β on proliferating hippocampal neural progenitor cells.

Keywords: Nr2e1; inflammation; neurogenesis; nuclear receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation*
  • Cells, Cultured
  • Gene Expression Regulation*
  • Hippocampus / cytology
  • Hippocampus / metabolism*
  • Interleukin-1beta / metabolism*
  • NF-kappa B / metabolism
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism*
  • Neurogenesis
  • Rats
  • Receptors, Cytoplasmic and Nuclear / biosynthesis*
  • Signal Transduction
  • Spheroids, Cellular / cytology
  • Spheroids, Cellular / metabolism

Substances

  • IL1B protein, rat
  • Interleukin-1beta
  • NF-kappa B
  • NR2E1 protein, rat
  • Receptors, Cytoplasmic and Nuclear