Axotomy-induced miR-21 promotes axon growth in adult dorsal root ganglion neurons

PLoS One. 2011;6(8):e23423. doi: 10.1371/journal.pone.0023423. Epub 2011 Aug 10.

Abstract

Following injury, dorsal root ganglion (DRG) neurons undergo transcriptional changes so as to adopt phenotypic changes that promote cell survival and axonal regeneration. Here we used a microarray approach to profile changes in a population of small noncoding RNAs known as microRNAs (miRNAs) in the L4 and L5 DRG following sciatic nerve transection. Results showed that 20 miRNA transcripts displayed a significant change in expression levels, with 8 miRNAs transcripts being altered by more than 1.5-fold. Using quantitative reverse transcription PCR, we demonstrated that one of these miRNAs, miR-21, was upregulated by 7-fold in the DRG at 7 days post-axotomy. In dissociated adult rat DRG neurons lentiviral vector-mediated overexpression of miR-21 promoted neurite outgrowth on a reduced laminin substrate. miR-21 directly downregulated expression of Sprouty2 protein, as confirmed by Western blot analysis and 3' untranslated region (UTR) luciferase assays. Our data show that miR-21 is an axotomy-induced miRNA that enhances axon growth, and suggest that miRNAs are important players in regulating growth pathways following peripheral nerve injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Aging / metabolism*
  • Animals
  • Axons / metabolism*
  • Axotomy*
  • Ganglia, Spinal / metabolism*
  • Gene Expression Profiling
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurites / metabolism
  • Neurites / pathology
  • Protein Serine-Threonine Kinases
  • Rats
  • Rats, Wistar
  • Sciatic Nerve / injuries
  • Sciatic Nerve / metabolism
  • Sciatic Nerve / pathology
  • Up-Regulation / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • Intracellular Signaling Peptides and Proteins
  • MIRN21 microRNA, mouse
  • Membrane Proteins
  • MicroRNAs
  • Nerve Tissue Proteins
  • Spry2 protein, rat
  • mirn21 microRNA, rat
  • Protein Serine-Threonine Kinases
  • Spry2 protein, mouse