SLC17A9 protein functions as a lysosomal ATP transporter and regulates cell viability

J Biol Chem. 2014 Aug 15;289(33):23189-23199. doi: 10.1074/jbc.M114.567107. Epub 2014 Jun 24.

Abstract

Lysosomes contain abundant ATP, which is released through lysosomal exocytosis following exposure to various stimuli. However, the molecular mechanisms underlying lysosomal ATP accumulation remain unknown. The vesicular nucleotide transporter, also known as solute carrier family 17 member 9 (SLC17A9), has been shown to function in ATP transport across secretory vesicles/granules membrane in adrenal chromaffin cells, T cells, and pancreatic cells. Here, using mammalian cell lines, we report that SLC17A9 is highly enriched in lysosomes and functions as an ATP transporter in those organelles. SLC17A9 deficiency reduced lysosome ATP accumulation and compromised lysosome function, resulting in cell death. Our data suggest that SLC17A9 activity mediates lysosomal ATP accumulation and plays an important role in lysosomal physiology and cell viability.

Keywords: ATP; Cell Death; Lysosome; Transporter; Vacuolar ATPase; Vesicular Nucleotide Transporter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / genetics
  • Adenosine Triphosphate / metabolism*
  • Animals
  • Biological Transport, Active / physiology
  • COS Cells
  • Cell Death
  • Cell Survival / physiology
  • Chlorocebus aethiops
  • Chromaffin Cells / cytology
  • Chromaffin Cells / metabolism
  • HEK293 Cells
  • Humans
  • Lysosomes / genetics
  • Lysosomes / metabolism*
  • Nucleotide Transport Proteins / genetics
  • Nucleotide Transport Proteins / metabolism*
  • Pancreas / cytology
  • Pancreas / metabolism
  • T-Lymphocytes / cytology
  • T-Lymphocytes / metabolism

Substances

  • Nucleotide Transport Proteins
  • Slc17a9 protein, human
  • Adenosine Triphosphate