Cell Reports (Sep 2017)

Changes in the Coding and Non-coding Transcriptome and DNA Methylome that Define the Schwann Cell Repair Phenotype after Nerve Injury

  • Peter J. Arthur-Farraj,
  • Claire C. Morgan,
  • Martyna Adamowicz,
  • Jose A. Gomez-Sanchez,
  • Shaline V. Fazal,
  • Anthony Beucher,
  • Bonnie Razzaghi,
  • Rhona Mirsky,
  • Kristjan R. Jessen,
  • Timothy J. Aitman

DOI
https://doi.org/10.1016/j.celrep.2017.08.064
Journal volume & issue
Vol. 20, no. 11
pp. 2719 – 2734

Abstract

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Repair Schwann cells play a critical role in orchestrating nerve repair after injury, but the cellular and molecular processes that generate them are poorly understood. Here, we perform a combined whole-genome, coding and non-coding RNA and CpG methylation study following nerve injury. We show that genes involved in the epithelial-mesenchymal transition are enriched in repair cells, and we identify several long non-coding RNAs in Schwann cells. We demonstrate that the AP-1 transcription factor C-JUN regulates the expression of certain micro RNAs in repair Schwann cells, in particular miR-21 and miR-34. Surprisingly, unlike during development, changes in CpG methylation are limited in injury, restricted to specific locations, such as enhancer regions of Schwann cell-specific genes (e.g., Nedd4l), and close to local enrichment of AP-1 motifs. These genetic and epigenomic changes broaden our mechanistic understanding of the formation of repair Schwann cell during peripheral nervous system tissue repair.

Keywords