Parkinson's disease-risk protein TMEM175 is a proton-activated proton channel in lysosomes

Cell. 2022 Jun 23;185(13):2292-2308.e20. doi: 10.1016/j.cell.2022.05.021.

Abstract

Lysosomes require an acidic lumen between pH 4.5 and 5.0 for effective digestion of macromolecules. This pH optimum is maintained by proton influx produced by the V-ATPase and efflux through an unidentified "H+ leak" pathway. Here we show that TMEM175, a genetic risk factor for Parkinson's disease (PD), mediates the lysosomal H+ leak by acting as a proton-activated, proton-selective channel on the lysosomal membrane (LyPAP). Acidification beyond the normal range potently activated LyPAP to terminate further acidification of lysosomes. An endogenous polyunsaturated fatty acid and synthetic agonists also activated TMEM175 to trigger lysosomal proton release. TMEM175 deficiency caused lysosomal over-acidification, impaired proteolytic activity, and facilitated α-synuclein aggregation in vivo. Mutational and pH normalization analyses indicated that the channel's H+ conductance is essential for normal lysosome function. Thus, modulation of LyPAP by cellular cues may dynamically tune the pH optima of endosomes and lysosomes to regulate lysosomal degradation and PD pathology.

Keywords: Proton channel; acidification; degradation; lysosome; pH optimum.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endosomes / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Intracellular Membranes / metabolism
  • Lysosomes / metabolism
  • Parkinson Disease* / metabolism
  • Potassium Channels / metabolism
  • Protons

Substances

  • Potassium Channels
  • Protons
  • TMEM175 protein, human