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

Author:

Wang Wuyang1ORCID,Zhang Xiaoli1,Gao Qiong1ORCID,Lawas Maria1,Yu Lu1,Cheng Xiping1,Gu Mingxue1,Sahoo Nirakar1,Li Xinran1,Li Ping12,Ireland Stephen1,Meredith Andrea3,Xu Haoxing1ORCID

Affiliation:

1. Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109

2. Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, China

3. Department of Physiology, University of Maryland School of Medicine, Baltimore, MD 21201

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.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Cell Biology

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