A voltage-dependent K+ channel in the lysosome is required for refilling lysosomal Ca2+ stores

J Cell Biol. 2017 Jun 5;216(6):1715-1730. doi: 10.1083/jcb.201612123. Epub 2017 May 3.

Abstract

The resting membrane potential (Δψ) of the cell is negative on the cytosolic side and determined primarily by the plasma membrane's selective permeability to K+ We show that lysosomal Δψ is set by lysosomal membrane permeabilities to Na+ and H+, but not K+, and is positive on the cytosolic side. An increase in juxta-lysosomal Ca2+ rapidly reversed lysosomal Δψ by activating a large voltage-dependent and K+-selective conductance (LysoKVCa). LysoKVCa is encoded molecularly by SLO1 proteins known for forming plasma membrane BK channels. Opening of single LysoKVCa channels is sufficient to cause the rapid, striking changes in lysosomal Δψ. Lysosomal Ca2+ stores may be refilled from endoplasmic reticulum (ER) Ca2+ via ER-lysosome membrane contact sites. We propose that LysoKVCa serves as the perilysosomal Ca2+ effector to prime lysosomes for the refilling process. Consistently, genetic ablation or pharmacological inhibition of LysoKVCa, or abolition of its Ca2+ sensitivity, blocks refilling and maintenance of lysosomal Ca2+ stores, resulting in lysosomal cholesterol accumulation and a lysosome storage phenotype.

MeSH terms

  • Animals
  • COS Cells
  • Calcium / metabolism*
  • Cell Line, Tumor
  • Chlorocebus aethiops
  • Cholesterol / metabolism
  • Endoplasmic Reticulum / metabolism
  • Genotype
  • HEK293 Cells
  • Humans
  • Ion Channel Gating
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits / antagonists & inhibitors
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits / genetics
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits / metabolism*
  • Lysosomes / drug effects
  • Lysosomes / metabolism*
  • Membrane Potentials
  • Mice, Knockout
  • Phenotype
  • Potassium Channel Blockers / pharmacology
  • Potassium Channels, Voltage-Gated / antagonists & inhibitors
  • Potassium Channels, Voltage-Gated / metabolism*
  • Protein Transport
  • Time Factors
  • Transfection

Substances

  • Kcnma1 protein, mouse
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
  • Potassium Channel Blockers
  • Potassium Channels, Voltage-Gated
  • Cholesterol
  • Calcium