Protein kinase C theta (Prkcq) affects nerve degeneration and regeneration through the c-fos and c-jun pathways in injured rat sciatic nerves

Exp Neurol. 2021 Dec:346:113843. doi: 10.1016/j.expneurol.2021.113843. Epub 2021 Aug 19.

Abstract

Background: Previous finding using DNA microarray and bioinformatics analysis, we have reported some key factors which regulated gene expression and signaling pathways in injured sciatic nerve during Wallerian Degeneration (WD). This research is focused on protein kinase C theta (Prkcq) participates in the regulation of the WD process.

Methods: In this study, we explored the molecular mechanism by which Prkcq in Schwann cells (SCs) affects nerve degeneration and regeneration in vivo and in vitro after rat sciatic nerve injury.

Results: Study of the cross-sectional model showed that Prkcq expression decreased significantly during sciatic nerve repair. Functional analysis showed that upregulation and downregulation of Prkcq could affect the proliferation, migration and apoptosis of Schwann cells and lead to the expression of related factors through the activation of the β-catenin, c-fos, and p-c-jun/c-jun pathways.

Conclusion: The study provides insights into the role of Prkcq in early WD during peripheral nerve degeneration and/or regeneration.

Keywords: Nerve regeneration; Prkcq; Rat; Schwann cells; Sciatic nerve injury; Wallerian degeneration (WD).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • JNK Mitogen-Activated Protein Kinases / biosynthesis*
  • Male
  • Nerve Degeneration / metabolism*
  • Nerve Degeneration / pathology
  • Nerve Regeneration / physiology*
  • Protein Kinase C-theta / biosynthesis*
  • Proto-Oncogene Proteins c-fos / biosynthesis*
  • Rats
  • Schwann Cells / metabolism
  • Schwann Cells / pathology
  • Sciatic Nerve / injuries
  • Sciatic Nerve / metabolism
  • Sciatic Nerve / pathology
  • Sciatic Neuropathy / metabolism*
  • Sciatic Neuropathy / pathology
  • Signal Transduction / physiology

Substances

  • Proto-Oncogene Proteins c-fos
  • Protein Kinase C-theta
  • JNK Mitogen-Activated Protein Kinases