4.7 Article

Renal Deletion of LRRC8/VRAC Channels Induces Proximal Tubulopathy

Journal

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Volume 33, Issue 8, Pages 1528-1545

Publisher

AMER SOC NEPHROLOGY
DOI: 10.1681/ASN.2021111458

Keywords

VSOR; RVD; transepithelial; glycosuria; chloride channel; Cl-? channel; lysosome; Fanconi-like syndrome

Funding

  1. European Research Council Advanced Grant VOLSIGNAL [740537]
  2. Deutsche Forschungsgemeinschaft [SFB 1365]
  3. Fondation Louis-Jeantet (Prix Louis-Jeantet de Medecine) [2000]

Ask authors/readers for more resources

This study found that VRAC/LRRC8 channels play an important role in the kidney, particularly in the function and integrity of proximal tubules. LRRC8 channels may be crucial for the basolateral exit of many organic compounds.
Background Volume-regulated anion channels (VRACs) are heterohexamers of LRRC8A with LRRC8B, -C, -D, or -E in various combinations. Depending on the subunit composition, these swelling-activated channels conduct chloride, amino acids, organic osmolytes, and drugs. Despite VRACs' role in cell volume regulation, and large osmolarity changes in the kidney, neither the localization nor the function of VRACs in the kidney is known. Methods Mice expressing epitope-tagged LRRC8 subunits were used to determine the renal localization of all VRAC subunits. Mice carrying constitutive deletions of Lrrc8b-e, or with inducible or cell-specific ablation of Lrrc8a, were analyzed to assess renal functions of VRACs. Analysis included histology, urine and serum parameters in different diuresis states, and metabolomics. Results The kidney expresses all five VRAC subunits with strikingly distinct localization. Whereas LRRC8C is exclusively found in vascular endothelium, all other subunits are found in the nephron. LRRC8E is specific for intercalated cells, whereas LRRC8A, LRRC8B, and LRRC8D are prominent in basolateral membranes of proximal tubules. Conditional deletion of LRRC8A in proximal but not distal tubules and constitutive deletion of LRRC8D cause proximal tubular injury, increased diuresis, and mild Fanconi-like symptoms. Conclusions VRAC/LRRC8 channels are crucial for the function and integrity of proximal tubules, but not for more distal nephron segments despite their larger need for volume regulation. LRRC8A/D channels may be required for the basolateral exit of many organic compounds, including cellular metabolites, in proximal tubules. Proximal tubular injury likely results from combined accumulation of several transported molecules in the absence of VRAC channels.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available