Neuritin promotes neurite and spine growth in rat cerebellar granule cells via L-type calcium channel-mediated calcium influx

J Neurochem. 2018 Oct;147(1):40-57. doi: 10.1111/jnc.14535. Epub 2018 Aug 16.

Abstract

Neuritin is a neurotrophic factor that is activated by neural activity and neurotrophins. Its major function is to promote neurite growth and branching; however, the underlying mechanisms are not fully understood. To address this issue, this study investigated the effects of neuritin on neurite and spine growth and intracellular Ca2+ concentration in rat cerebellar granule neurons (CGNs). Incubation of CGNs for 24 h with neuritin increased neurite length and spine density; this effect was mimicked by insulin and abolished by inhibiting insulin receptor (IR) or mitogen-activated protein kinase kinase/extracellular signal-regulated kinase (ERK) activity. Calcium imaging and western blot analysis revealed that neuritin enhanced the increase in intracellular Ca2+ level induced by high K+ , and stimulated the cell surface expression of CaV 1.2 and CaV 1.3 α subunits of the L-type calcium channel, which was suppressed by inhibition of IR or mitogen-activated protein kinase kinase/ERK. Treatment with inhibitors of L-type calcium channels, calmodulin, and calcineurin (CaN) abrogated the effects of neuritin on neurite length and spine density. A similar result was obtained by silencing nuclear factor of activated T cells c4, which is known to be activated by neuritin in CGNs. These results indicate that IR and ERK signaling as well as the Ca2+ /CaN/nuclear factor of activated T cells c4 axis mediate the effects of neuritin on neurite and spine growth in CGNs.

Open practices: Open Science: This manuscript was awarded with the Open Materials Badge. For more information see: https://cos.io/our-services/open-science-badges/ Cover Image for this issue: doi: 10.1111/jnc.14195.

Keywords: Ca2+-CaN-NFATc4 axis; L-type calcium channel; cerebellar granule neurons; insulin receptor; neurite and spine growth; neuritin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium Channels / metabolism
  • Calcium Channels, L-Type / drug effects*
  • Calcium Channels, L-Type / metabolism
  • Calcium Signaling / drug effects*
  • Cerebellum / cytology*
  • Cerebellum / drug effects
  • Cerebellum / growth & development
  • Cytoplasmic Granules / drug effects
  • Dendritic Spines / drug effects*
  • Female
  • GPI-Linked Proteins / pharmacology
  • Gene Silencing
  • Humans
  • Insulin / pharmacology
  • MAP Kinase Signaling System / drug effects
  • NFATC Transcription Factors / antagonists & inhibitors
  • NFATC Transcription Factors / genetics
  • Neurites / drug effects*
  • Neuropeptides / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Insulin / antagonists & inhibitors

Substances

  • Calcium Channels
  • Calcium Channels, L-Type
  • GPI-Linked Proteins
  • Insulin
  • L-type calcium channel alpha(1C)
  • NFATC Transcription Factors
  • Neuropeptides
  • Nrn1 protein, rat
  • Cacna1d protein, rat
  • Receptor, Insulin