Lysosomal Acidification Mechanisms

被引:927
作者
Mindell, Joseph A. [1 ]
机构
[1] Natl Inst Neurol Disorders & Stroke, Membrane Transport Biophys Sect, NIH, Bethesda, MD 20892 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 74 | 2012年 / 74卷
关键词
V-ATPase; transporter; ClC-7; channel; counterion; VACUOLAR H+-ATPASE; AUTOSOMAL-DOMINANT OSTEOPETROSIS; CHLORIDE CHANNEL; PROTON PUMP; YEAST VACUOLAR; PROKARYOTIC HOMOLOG; STORAGE DISEASE; GENE ENCODES; SUBUNIT; CLC-7;
D O I
10.1146/annurev-physiol-012110-142317
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Lysosomes, the terminal organelles on the endocytic pathway, digest macromolecules and make their components available to the cell as nutrients. Hydrolytic enzymes specific to a wide range of targets reside within the lysosome; these enzymes are activated by the highly acidic pH (between 4.5 and 5.0) in the organelles' interior. Lysosomes generate and maintain their pH gradients by using the activity of a proton-pumping V-type ATPase, which uses metabolic energy in the form of ATP to pump protons into the lysosome lumen. Because this activity separates electric charge and generates a transmembrane voltage, another ion must move to dissipate this voltage for net pumping to occur. This so-called counterion may be either a cation (moving out of the lysosome) or an anion (moving into the lysosome). Recent data support the involvement of ClC-7, a Cl-/H+ antiporter, in this process, although many open questions remain as to this transporter's involvement. Although functional results also point to a cation transporter, its molecular identity remains uncertain. Both the V-ATPase and the counterion transporter are likely to be important players in the mechanisms determining the steady-state pH of the lysosome interior. Exciting new results suggest that lysosomal pH may be dynamically regulated in some cell types.
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收藏
页码:69 / 86
页数:18
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