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The volume-regulated anion channel (LRRC8) in nodose neurons is sensitive to acidic pH
Runping Wang, Yongjun Lu, Susheel Gunasekar, Yanhui Zhang, Christopher J. Benson, Mark W. Chapleau, Rajan Sah, François M. Abboud
Runping Wang, Yongjun Lu, Susheel Gunasekar, Yanhui Zhang, Christopher J. Benson, Mark W. Chapleau, Rajan Sah, François M. Abboud
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Research Article Cell biology

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

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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

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Figure 5

ROS generation during the pHo-conditioned current.

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ROS generation during the pHo-conditioned current.
The images in A and B...
The images in A and B represent the bright fields and dihydroethidium (DHE) fluorescence images of 2 different cultures of nodose neurons. (A) The cells were observed for up to 30 minutes after DHE loading in a bath solution at pHo 7.4, without exposing them to low pHo 6.0 (control). (B) The cells were loaded with DHE and then exposed transiently to pHo 6.0. The middle image shows minimal fluorescence before exposure to pHo 6.0, and the right image shows pronounced fluorescence approximately 10 minutes after exposure to pHo 6.0. The corresponding graphs (C and D) show that after loading with DHE (large black arrows); the slope of spontaneous fluorescence seen over 30 minutes without exposure to low pHo is minimal in C (control cells) as reflected in the third fluorescence image in A. (D) The slope is dramatically increased following the 3 transient exposures to pHo 6.0 (small red arrows) as reflected in fluorescence image in B. The dot plot shows the slopes of fluorescence of individual neurons averaging 0.04 ± 0.01 units/min before and 0.12 ± 0.02 units/min after exposure to low pHo (n = 31 neurons from 2 mice, **P < 0.01 compared with before exposure). Statistical comparison is a paired 2-tailed Student’s t test.

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ISSN 2379-3708

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