Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • Resource and Technical Advances
    • Clinical Medicine
    • Reviews
    • Editorials
    • Perspectives
    • Top read articles
  • JCI This Month
    • Current issue
    • Past issues

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Editorials
  • Viewpoint
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising
  • Job board
  • Contact
The volume-regulated anion channel (LRRC8) in nodose neurons is sensitive to acidic pH
Runping Wang, … , Rajan Sah, François M. Abboud
Runping Wang, … , Rajan Sah, François M. Abboud
Published March 9, 2017
Citation Information: JCI Insight. 2017;2(5):e90632. https://doi.org/10.1172/jci.insight.90632.
View: Text | PDF
Research Article Cell biology

The volume-regulated anion channel (LRRC8) in nodose neurons is sensitive to acidic pH

  • Text
  • PDF
Abstract

The leucine rich repeat containing protein 8A (LRRC8A), or SWELL1, is an essential component of the volume-regulated anion channel (VRAC) that is activated by cell swelling and ionic strength. We report here for the first time to our knowledge its expression in a primary cell culture of nodose ganglia neurons and its localization in the soma, neurites, and neuronal membrane. We show that this neuronal VRAC/SWELL1 senses low external pH (pHo) in addition to hypoosmolarity. A robust sustained chloride current is seen in 77% of isolated nodose neurons following brief exposures to extracellular acid pH. Its activation involves proton efflux, intracellular alkalinity, and an increase in NOX-derived H2O2. The molecular identity of both the hypoosmolarity-induced and acid pHo–conditioned VRAC as LRRC8A (SWELL1) was confirmed by Cre-flox–mediated KO, shRNA-mediated knockdown, and CRISPR/Cas9-mediated LRRC8A deletion in HEK cells and in primary nodose neuronal cultures. Activation of VRAC by low pHo reduces neuronal injury during simulated ischemia and N-methyl-D-aspartate–induced (NMDA-induced) apoptosis. These results identify the VRAC (LRRC8A) as a dual sensor of hypoosmolarity and low pHo in vagal afferent neurons and define the mechanisms of its activation and its neuroprotective potential.

Authors

Runping Wang, Yongjun Lu, Susheel Gunasekar, Yanhui Zhang, Christopher J. Benson, Mark W. Chapleau, Rajan Sah, François M. Abboud

×

Figure 1

A prolonged pHo-conditioned inward current and depolarizations.

Options: View larger image (or click on image) Download as PowerPoint
A prolonged pHo-conditioned inward current and depolarizations.
(A) A re...
(A) A representative inward current evoked from a nodose neuron after 3 brief sequential exposures to extracellular pHo 6.0, indicated by the vertical black arrows. The membrane potential was held at –60 mV. The peak currents seen in 17 of 22 individual neurons are shown. The current density is pHo dependent and averaged 8.5 ± 2.1 pA/pF for pHo 7.0 (n = 2 mice); 10.8 ± 2.9 pA/pF for pHo 6.5 (n = 2 mice); 21.2 ± 2.7 pA/pF for pHo 6.0 (n = 6 mice, P = 0.037 by ANOVA). (B) The currents evoked in control solutions (21.2 ± 2.7 pA/pF, n = 3 mice) are maintained in extracellular Ca2+ and Na+ free solution (19.3 ± 3.1 pA/pF, n = 3 mice), in intracellular K+ free solutions (17.4 ± 4.2 pA/pF, n = 5 mice ), and in solutions free of all permeable cations (25.9 ± 6.6 pA/pF, n = 3 mice ) but are absent in solutions of 4 mM intracellular Cl– (0.6 ± 0.2 pA/pF, n = 5 mice, **P < 0.001 vs. control by ANOVA). (C) Under current clamp conditions, progressive depolarizations and action potentials were evoked following the transient sequential pHo 6.0 applications (black arrows). The tracing and panel to the left show the mean maximum depolarizations of 35.2 ± 4.4 mV (n = 5 mice) at equimolar (133 mM) [Cl–]i and [Cl–]o and an equilibrium potential of ~0 mV. The tracing and panel to the right show the membrane potential and maximum depolarizations recorded with the perforated patch clamp using gramicidin to maintain physiologic intracellular [Cl–]i and an equilibrium potential that is more negative hence a lesser maximal depolarization (12.7 ± 3.4 mV, n = 2 mice). All panels include responses of individual neurons and the means ± SE.

Copyright © 2023 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts