Up-regulation of protective neuronal MicroRNAs by FTY720 and novel FTY720-derivatives

Neurosci Lett. 2019 Jan 18:690:178-180. doi: 10.1016/j.neulet.2018.10.040. Epub 2018 Oct 22.

Abstract

In searching for Parkinson's disease (PD) pharmacotherapies we began studying FTY720, a food and drug administration (FDA) approved drug. We also created derivatives, FTY720-C2 and FTY720-Mitoxy, and began assessing them. Here we treated dopaminergic MN9D cells with FTY720s then measured microRNA (miRNA) levels by PCR arrays. We discovered that all three FTY720s increased miR376b-3p, while FTY720-C2 also increased miR-128-3p, miR-146b-5p, miR-7a-5p, and miR-9-5p, and FTY720-Mitoxy also increased miR-30d-5p. Investigations revealed that some miRNAs downregulate alpha-synuclein, while others reduce apoptosis, suggesting that FTY720s may act to reduce synucleinopathy and dopaminergic neuron loss in PD and related disorders.

Keywords: Dopaminergic MN9D cells; Neuroprotection; miRNA upregulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Ceramides / pharmacology*
  • Dopaminergic Neurons / metabolism*
  • Fingolimod Hydrochloride / analogs & derivatives*
  • Fingolimod Hydrochloride / pharmacology*
  • Mice
  • MicroRNAs / metabolism*
  • Neuroprotective Agents / metabolism*
  • Up-Regulation / drug effects*

Substances

  • Ceramides
  • MicroRNAs
  • Neuroprotective Agents
  • fty720-c2
  • fty720-mitoxy
  • Fingolimod Hydrochloride