The H+-ATPase (V-ATPase): from proton pump to signaling complex in health and disease

Am J Physiol Cell Physiol. 2021 Mar 1;320(3):C392-C414. doi: 10.1152/ajpcell.00442.2020. Epub 2020 Dec 16.

Abstract

A primary function of the H+-ATPase (or V-ATPase) is to create an electrochemical proton gradient across eukaryotic cell membranes, which energizes fundamental cellular processes. Its activity allows for the acidification of intracellular vesicles and organelles, which is necessary for many essential cell biological events to occur. In addition, many specialized cell types in various organ systems such as the kidney, bone, male reproductive tract, inner ear, olfactory mucosa, and more, use plasma membrane V-ATPases to perform specific activities that depend on extracellular acidification. It is, however, increasingly apparent that V-ATPases are central players in many normal and pathophysiological processes that directly influence human health in many different and sometimes unexpected ways. These include cancer, neurodegenerative diseases, diabetes, and sensory perception, as well as energy and nutrient-sensing functions within cells. This review first covers the well-established role of the V-ATPase as a transmembrane proton pump in the plasma membrane and intracellular vesicles and outlines factors contributing to its physiological regulation in different cell types. This is followed by a discussion of the more recently emerging unconventional roles for the V-ATPase, such as its role as a protein interaction hub involved in cell signaling, and the (patho)physiological implications of these interactions. Finally, the central importance of endosomal acidification and V-ATPase activity on viral infection will be discussed in the context of the current COVID-19 pandemic.

Keywords: acidification; endosomal trafficking; pH regulation; pathophysiology; proton pumping ATPase.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Angiotensin-Converting Enzyme 2 / metabolism
  • COVID-19 / virology*
  • Humans
  • Proton-Translocating ATPases / genetics
  • Proton-Translocating ATPases / metabolism*
  • SARS-CoV-2*
  • Signal Transduction
  • Virus Internalization

Substances

  • Angiotensin-Converting Enzyme 2
  • Proton-Translocating ATPases