A novel Drosophila injury model reveals severed axons are cleared through a Draper/MMP-1 signaling cascade

Elife. 2017 Aug 21:6:e23611. doi: 10.7554/eLife.23611.

Abstract

Neural injury triggers swift responses from glia, including glial migration and phagocytic clearance of damaged neurons. The transcriptional programs governing these complex innate glial immune responses are still unclear. Here, we describe a novel injury assay in adult Drosophila that elicits widespread glial responses in the ventral nerve cord (VNC). We profiled injury-induced changes in VNC gene expression by RNA sequencing (RNA-seq) and found that responsive genes fall into diverse signaling classes. One factor, matrix metalloproteinase-1 (MMP-1), is induced in Drosophila ensheathing glia responding to severed axons. Interestingly, glial induction of MMP-1 requires the highly conserved engulfment receptor Draper, as well as AP-1 and STAT92E. In MMP-1 depleted flies, glia do not properly infiltrate neuropil regions after axotomy and, as a consequence, fail to clear degenerating axonal debris. This work identifies Draper-dependent activation of MMP-1 as a novel cascade required for proper glial clearance of severed axons.

Keywords: D. melanogaster; Draper; Wallerian degeneration; extracellular matrix; glial immunity; matrix metalloproteinase; neuroscience.

MeSH terms

  • Animals
  • Disease Models, Animal
  • Drosophila / physiology*
  • Drosophila Proteins / metabolism*
  • Gene Expression Profiling
  • Matrix Metalloproteinase 1 / metabolism*
  • Membrane Proteins / metabolism*
  • Neuroglia / physiology*
  • Peripheral Nerve Injuries / physiopathology*
  • STAT Transcription Factors / metabolism
  • Sequence Analysis, RNA
  • Signal Transduction*
  • Transcription Factor AP-1 / metabolism

Substances

  • Drosophila Proteins
  • Membrane Proteins
  • STAT Transcription Factors
  • Stat92E protein, Drosophila
  • Transcription Factor AP-1
  • drpr protein, Drosophila
  • Matrix Metalloproteinase 1