Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney
Festa, Beatrice Paola; Chen, Zhiyong; Berquez, Marine; Debaix, Huguette; Tokonami, Natsuko; Prange, Jenny Ann; Hoek, Glenn Van De; Alessio, Cremonesi; Raimondi, Andrea; Nevo, Nathalie; Giles, Rachel H.; Devuyst, Olivier; Luciani, Alessandro
(2018) Nature Communications [E], volume 9, issue 1
(Article)
Abstract
The endolysosomal system sustains the reabsorptive activity of specialized epithelial cells. Lysosomal storage diseases such as nephropathic cystinosis cause a major dysfunction of epithelial cells lining the kidney tubule, resulting in massive losses of vital solutes in the urine. The mechanisms linking lysosomal defects and epithelial dysfunction remain unknown, preventing
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the development of disease-modifying therapies. Here we demonstrate, by combining genetic and pharmacologic approaches, that lysosomal dysfunction in cystinosis results in defective autophagy-mediated clearance of damaged mitochondria. This promotes the generation of oxidative stress that stimulates Gα12/Src-mediated phosphorylation of tight junction ZO-1 and triggers a signaling cascade involving ZO-1-associated Y-box factor ZONAB, which leads to cell proliferation and transport defects. Correction of the primary lysosomal defect, neutralization of mitochondrial oxidative stress, and blockage of tight junction-associated ZONAB signaling rescue the epithelial function. We suggest a link between defective lysosome-autophagy degradation pathways and epithelial dysfunction, providing new therapeutic perspectives for lysosomal storage disorders.
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Keywords: Fanconi syndrome, Lysosomes, Macroautophagy, Mechanisms of disease, General Chemistry, General Biochemistry,Genetics and Molecular Biology, General Physics and Astronomy
ISSN: 2041-1723
Publisher: Nature Publishing Group
Note: Funding Information: We are grateful to Fonds National de la Recherche Scientifique and the Fonds de la Recherche Scientifique Médicale (Brussels, Belgium), the European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreement number 305608 (EURenOmics) and under the grant agreement number 608847 (IKPP2), the Cystinosis Research Foundation (Irvine, CA, USA), the Swiss National Science Foundation (project grant 31003A-169850), the clinical research priority programs (KFSP) Molecular Imaging Network Zurich (MINZ) and RADIZ (Rare Disease Initiative Zurich) of the UZH, the Dutch Kidney Foundation (project grant 16OI06) and the Swiss National Centre of Competence in Research (NCCR) Kidney Control of Homeostasis (Kidney.CH) for support and Junior Grant (to A.L.). We acknowledge Benjamin Klor-mann and Ive Logister for providing technical assistance; the Hubrecht Institute Zebrafish Caretaker team; Corinne Antignac (Imagine, Paris) for fruitful discussions and for providing the Ctns mice; and Pierre Verroust and Renata Kozyraki for providing reagents. We thank ALEMBIC facility at San Raffaele Scientific Institute (Milan, Italy) for providing EM assistance. Imaging was performed with equipment maintained by the Center for Microscopy and Image Analysis, University of Zurich. Publisher Copyright: © 2018 The Author(s).
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