A Pvr-AP-1-Mmp1 signaling pathway is activated in astrocytes upon traumatic brain injury

Elife. 2024 Oct 31:12:RP87258. doi: 10.7554/eLife.87258.

Abstract

Traumatic brain injury (TBI) caused by external mechanical forces is a major health burden worldwide, but the underlying mechanism in glia remains largely unclear. We report herein that Drosophila adults exhibit a defective blood-brain barrier, elevated innate immune responses, and astrocyte swelling upon consecutive strikes with a high-impact trauma device. RNA sequencing (RNA-seq) analysis of these astrocytes revealed upregulated expression of genes encoding PDGF and VEGF receptor-related (Pvr, a receptor tyrosine kinase), adaptor protein complex 1 (AP-1, a transcription factor complex of the c-Jun N-terminal kinase pathway) composed of Jun-related antigen (Jra) and kayak (kay), and matrix metalloproteinase 1 (Mmp1) following TBI. Interestingly, Pvr is both required and sufficient for AP-1 and Mmp1 upregulation, while knockdown of AP-1 expression in the background of Pvr overexpression in astrocytes rescued Mmp1 upregulation upon TBI, indicating that Pvr acts as the upstream receptor for the downstream AP-1-Mmp1 transduction. Moreover, dynamin-associated endocytosis was found to be an important regulatory step in downregulating Pvr signaling. Our results identify a new Pvr-AP-1-Mmp1 signaling pathway in astrocytes in response to TBI, providing potential targets for developing new therapeutic strategies for TBI.

Keywords: D. melanogaster; Drosophila; Pvr; RNA-seq; astrocytes; matrix metalloproteinase; neuroscience; traumatic brain injury.

MeSH terms

  • Animals
  • Astrocytes* / metabolism
  • Brain Injuries, Traumatic* / genetics
  • Brain Injuries, Traumatic* / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster / metabolism
  • Matrix Metalloproteinase 1* / genetics
  • Matrix Metalloproteinase 1* / metabolism
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Signal Transduction*
  • Transcription Factor AP-1* / genetics
  • Transcription Factor AP-1* / metabolism

Substances

  • Transcription Factor AP-1
  • Matrix Metalloproteinase 1
  • Drosophila Proteins
  • Receptor Protein-Tyrosine Kinases

Associated data

  • GEO/GSE263447