TI-VAMP/VAMP7 is the SNARE of secretory lysosomes contributing to ATP secretion from astrocytes

Biol Cell. 2012 Apr;104(4):213-28. doi: 10.1111/boc.201100070. Epub 2012 Jan 11.

Abstract

Background information: ATP is the main transmitter stored and released from astrocytes under physiological and pathological conditions. Morphological and functional evidence suggest that besides secretory granules, secretory lysosomes release ATP. However, the molecular mechanisms involved in astrocytic lysosome fusion remain still unknown.

Results: In the present study, we identify tetanus neurotoxin-insensitive vesicle-associated membrane protein (TI-VAMP, also called VAMP7) as the vesicular SNARE which mediates secretory lysosome exocytosis, contributing to release of both ATP and cathepsin B from glial cells. We also demonstrate that fusion of secretory lysosomes is triggered by slow and locally restricted calcium elevations, distinct from calcium spikes which induce the fusion of glutamate-containing clear vesicles. Downregulation of TI-VAMP/VAMP7 expression inhibited the fusion of ATP-storing vesicles and ATP-mediated calcium wave propagation. TI-VAMP/VAMP7 downregulation also significantly reduced secretion of cathepsin B from glioma.

Conclusions: Given that sustained ATP release from glia upon injury greatly contributes to secondary brain damage and cathepsin B plays a critical role in glioma dissemination, TI-VAMP silencing can represent a novel strategy to control lysosome fusion in pathological conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • Astrocytes / cytology
  • Astrocytes / metabolism*
  • Calcium / metabolism*
  • Cathepsin B / metabolism*
  • Cerebral Cortex / cytology
  • Cerebral Cortex / embryology
  • Cerebral Cortex / metabolism
  • Down-Regulation
  • Embryo, Mammalian
  • Exocytosis
  • Glioma / metabolism
  • Glioma / pathology
  • Hippocampus / cytology
  • Hippocampus / embryology
  • Hippocampus / metabolism
  • Humans
  • Lysosomes / metabolism*
  • Membrane Fusion
  • Neuroglia / cytology
  • Neuroglia / metabolism
  • Primary Cell Culture
  • Protein Binding
  • R-SNARE Proteins / antagonists & inhibitors
  • R-SNARE Proteins / genetics
  • R-SNARE Proteins / metabolism*
  • RNA, Small Interfering / genetics
  • Rats
  • Signal Transduction
  • Transfection

Substances

  • R-SNARE Proteins
  • RNA, Small Interfering
  • VAMP7 protein, human
  • Vamp7 protein, rat
  • Adenosine Triphosphate
  • Cathepsin B
  • Calcium