The Hv1 proton channel responds to mechanical stimuli

Author:

Pathak Medha M.1,Tran Truc1,Hong Liang1,Joós Béla2,Morris Catherine E.3,Tombola Francesco1ORCID

Affiliation:

1. Department of Physiology and Biophysics, University of California, Irvine, CA 92697

2. Department of Physics, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada

3. Ottawa Hospital Research Institute, Ottawa, Ontario K1H 8M5, Canada

Abstract

The voltage-gated proton channel, Hv1, is expressed in tissues throughout the body and plays important roles in pH homeostasis and regulation of NADPH oxidase. Hv1 operates in membrane compartments that experience strong mechanical forces under physiological or pathological conditions. In microglia, for example, Hv1 activity is potentiated by cell swelling and causes an increase in brain damage after stroke. The channel complex consists of two proton-permeable voltage-sensing domains (VSDs) linked by a cytoplasmic coiled-coil domain. Here, we report that these VSDs directly respond to mechanical stimuli. We find that membrane stretch facilitates Hv1 channel opening by increasing the rate of activation and shifting the steady-state activation curve to less depolarized potentials. In the presence of a transmembrane pH gradient, membrane stretch alone opens the channel without the need for strong depolarizations. The effect of membrane stretch persists for several minutes after the mechanical stimulus is turned off, suggesting that the channel switches to a “facilitated” mode in which opening occurs more readily and then slowly reverts to the normal mode observed in the absence of membrane stretch. Conductance simulations with a six-state model recapitulate all the features of the channel’s response to mechanical stimulation. Hv1 mechanosensitivity thus provides a mechanistic link between channel activation in microglia and brain damage after stroke.

Funder

National Institutes of Health

University of California, Irvine

Natural Sciences and Engineering Research Council of Canada

Ottawa Hospital Research Institute

Publisher

Rockefeller University Press

Subject

Physiology

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