Lipid Peroxidation Drives Renal Cyst Growth In Vitro through Activation of TMEM16A

Schreiber R, Buchholz B, Kraus A, Schley G, Scholz J, Ousingsawat J, Kunzelmann K (2019)


Publication Type: Journal article

Publication year: 2019

Journal

Book Volume: 30

Pages Range: 228-242

Journal Issue: 2

DOI: 10.1681/ASN.2018010039

Abstract

Background Transepithelial chloride2 secretion, through the chloride channels cystic fibrosis transmembrane conductance regulator (CFTR) and TMEM16A (anoctamin 1), drives cyst enlargement in polycystic kidney disease (PKD). Polycystic kidneys are hypoxic, and oxidative stress activates TMEM16A. However, mechanisms for channel activation in PKD remain obscure.Methods Using tissue samples from patients with autosomal dominant PKD, embryonic kidney cultures, and anMDCK in vitro cyst model, we assessed peroxidation of plasmamembrane phospholipids in human and mouse polycystic kidneys. We also used electrophysiologic Ussing chamber and patch clamp experiments to analyze activation of TMEM16A and growth of renal cysts.Results Peroxidation of phospholipids in human and mouse kidneys as well as MDCK cysts in vitro is probably due to enhanced levels of reactive oxygen species. Lipid peroxidation correlated with increased cyst volume as shown in renal cultures and MDCK cysts in three-dimensional cultures. Reactive oxygen species and lipid peroxidation strongly activated TMEM16A, leading to depletion of calciumion stores and store-operated calcium influx. Activation of TMEM16A-and CFTR-dependent chloride secretion strongly augmented cyst growth. Exposure to scavengers of reactive oxygen species, such as glutathione, coenzyme Q10, or idebenone (a synthetic coenzyme Q10 homolog), as well as inhibition of oxidative lipid damage by ferrostatin-1 largely reduced activation of TMEM16A. Inhibition of TMEM16A reduced proliferation and fluid secretion in vitro.Conclusions These findings indicate that activation of TMEM16A by lipid peroxidation drives growth of renal cysts. We propose direct inhibition of TMEM16A or inhibition of lipid peroxidation as potentially powerful therapeutic approaches to delay cyst development in PKD.

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APA:

Schreiber, R., Buchholz, B., Kraus, A., Schley, G., Scholz, J., Ousingsawat, J., & Kunzelmann, K. (2019). Lipid Peroxidation Drives Renal Cyst Growth In Vitro through Activation of TMEM16A. Journal of the American Society of Nephrology, 30(2), 228-242. https://dx.doi.org/10.1681/ASN.2018010039

MLA:

Schreiber, Rainer, et al. "Lipid Peroxidation Drives Renal Cyst Growth In Vitro through Activation of TMEM16A." Journal of the American Society of Nephrology 30.2 (2019): 228-242.

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