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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 6

The pHo-conditioned Cl– current and VRAC are mediated by H2O2 and NADPH oxidase activation.

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The pHo-conditioned Cl– current and VRAC are mediated by H2O2 and NADPH ...
(A) The pHo-conditioned current is not blocked by a 30-minute application of 300 U/ml of the membrane permeable superoxide dismutase–polyethylene glycol (PEG-SOD) (20 ± 5 in control neurons, n = 3 mice, vs. 23 ± 5 pA/pF in neurons treated with SOD, n = 3 mice); (B) the current is blocked by 1,000 U/ml of the membrane permeable PEG-catalase (25.7 ± 6.9 in control neurons vs. 6.5 ± 1.5 pA/pF in neurons pretreated with catalase; n = 4 mice,*P < 0.05); and (C) the current is blocked in neurons pretreated with the inhibitors of NADPH oxidase apocynin (300 μM) and DPI (30 μM) (11.5 ± 1.9, n = 3 mice, in control vs. 3.7 ±0.l9, n = 3 mice, with apocynin,**P < 0.01, and vs. 5.0 ± 1.0 pA/pF, n = 3 mice, with DPI,*P < 0.05). (D) The current induced by hypoosmolarity (210 mOsm) is also blocked after exposure to PEG catalase (1,000 U/ml) (23.3 ± 6.3 vs. 0.6 ± 0.4 pA/pF before and after catalase, n = 2 mice,*P < 0.05). (E) H2O2 (1 mM) induces a current (19.2 ± 2.5 pA/pF, n = 3 mice) that is similar to both the pHo-conditioned (22.4 ± 4.0 pA/pF, n = 4 mice) and hypoosmolarity-induced currents, as in D. The panels represent responses of individual neurons and the means ± SE of each group. Unpaired 2-tailed Student’s t test, except for D, where the analysis was paired.

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