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

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

56 Citas (Scopus)

Resumen

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.

Idioma originalEnglish
Páginas (desde-hasta)23189-23199
Número de páginas11
PublicaciónJournal of Biological Chemistry
Volumen289
N.º33
DOI
EstadoPublished - ago. 15 2014

ASJC Scopus Subject Areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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