The critical role of endoplasmic reticulum stress and the stimulator of interferon genes (STING) pathway in kidney fi brosis

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Andrade-Silva, Magaiver ; Dhillon, Poonam ; Sanchez-Navarro, Andrea ; Mukhi, Dhanunjay ; Hu, Hailong ; Kolligundla, Lakshmi P. ; Bergeson, Andrea ; Abedini, Amin ; Levinsohn, Jonathan ; Dumoulin, Bernhard ; Camara, Niels O. S. ; Miner, Jonathan J. ; Susztak, Katalin

• Document type: Journal article
• Source: Kidney International; v. 107, n. 2, p. 15-pg., 2025-01-21.

Abstract

Endoplasmic reticulum (ER) stress is a condition in which the ER is overwhelmed and unable to manage its protein load properly. The precise activation mechanisms and role of ER stress in kidney disease remain unclear. To study this, we performed unbiased transcriptomics analysis to demonstrate ER stress in kidneys of patients with chronic kidney disease and in mouse models of acute and chronic kidney injury (cisplatin and unilateral ureteral obstruction and reanalyzed previously published data on folic acid and mitochondrial transcription factor A(TFAM) knockout mice). Inhibiting the protein kinase RNA-like ER kinase (PERK) arm of ER stress but not activating transcription factor 6 or inositol-requiring enzyme 1, protected mice from kidney fibrosis. The stimulator of interferon genes (STING) was identified as an important upstream activator of ER stress in kidney tubule cells. STING and PERK were found to physically interact, and STING agonists induced PERK activation in kidney tubule cells. Mice with a STING activating mutation presented with ER stress and kidney fibroinflammation. We also generated mice with a tubule specific STING deletion that were resistant to ER stress and kidney fibrosis. Human kidney spatial transcriptomics highlighted a spatial correlation between STING, ER stress and fibrotic gene expression. Thus, our results indicate that STING is an important upstream regulator of PERK and ER stress in tubule cells during kidney fibrosis development. (AU)

• FAPESP's process: 22/12517-7 - Unrevealing the molecular pathways triggered by the accumulation of intracellular DNA and RNA in diabetic kidney disease patients and mouse models of fibrosis
• Grantee: Magaiver Andrade Silva
• Support Opportunities: Scholarships abroad - Research Internship - Post-doctor