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

Qi Cao, Kexin Zhao, Xi Zoë Zhong, Yuanjie Zou, Haichuan Yu, Peng Huang, Tian Le Xu, Xian Ping Dong

Research output: Contribution to journalArticlepeer-review

56 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)23189-23199
Number of pages11
JournalJournal of Biological Chemistry
Volume289
Issue number33
DOIs
Publication statusPublished - Aug 15 2014

ASJC Scopus Subject Areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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