Mitochondrial Stress Links Environmental Triggers with Pro-Inflammatory Signaling in Crohn’s Disease
Authors:
- Flores Martín-ReyesFMFlores Martín-Reyes
- Manuel BernalMBManuel Bernal
- Cristina Rodríguez-DíazCRCristina Rodríguez-Díaz
- Damaris Rodríguez-De Los ReyesDRDamaris Rodríguez-De Los Reyes
- Ailec Ho-PlagaroAHAilec Ho-Plagaro
- Francisca Rodríguez-PachecoFRFrancisca Rodríguez-Pacheco
- Laura Camacho-MartelLCLaura Camacho-Martel
- Raquel Camargo-CameroRCRaquel Camargo-Camero
- Francisco J. Rodríguez-GonzálezFRFrancisco J. Rodríguez-González
- Guillermo Alcain-MartínezGAGuillermo Alcain-Martínez
- Rafael Martín-MasotRMRafael Martín-Masot
- Víctor M. Navas-LópezVNVíctor M. Navas-López
Open Access
- 13 December 2023
- journal article
- research article
- Published by MDPI AG in Antioxidants
- Vol. 12 (12) , 2105
Abstract
Inflammatory Bowel Diseases (IBD) are a group of chronic, inflammatory disorders of the gut. The incidence and activity of IBD are determined by both genetic and environmental factors. Among these factors, polymorphisms in genes related to autophagy and the consumption of non-steroidal anti-inflammatory drugs (NSAIDs) have been consistently associated with IBD. We show that NSAIDs induce mitochondrial stress and mitophagy in intestinal epithelial cells. In an altered mitophagy context simulating that observed in IBD patients, NSAID-induced mitochondrial stress leads to the release of mitochondrial components, which act as Danger Associated Molecular Patterns with pro-inflammatory potential. Furthermore, colonic organoids from Crohn’s disease patients and healthy donors show activation of the mitochondrial Unfolded Protein Response (UPRmt) upon treatment with ibuprofen. Finally, colon biopsies from Crohn’s disease patients in remission or with low-to-moderate activity also show expression of genes involved in UPRmt, while patients with severe activity show no increase compared to healthy donors. Our results suggest the involvement of mitochondria in the mechanisms triggering inflammation in IBD after NSAID use. Moreover, our results highlight the clinical relevance of mitochondrial stress and activation of the UPRmt pathway in the pathophysiology of Crohn’s disease.Keywords
Funding Information
- Ministerio de Ciencia, Innovación y Universidades (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- Instituto de Salud Carlos III (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- FEDER funds/Consejería de Economía y Conocimiento, Empresas y Universidad de la Junta de Andalucía (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- Consejería de Salud y Familia de la Junta de Andalucía (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- European Union (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- Nicolas Monardes program from the Consejería de Salud de Andalucía (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- ISCIII (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- Ministerio de Ciencia e Innovación (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
- Industria, Conocimiento y Universidades de Junta de Andalucía (IJCI-2017-31466, PI18/01652, UMA20-FEDERJA-081, PI-0244-2021, CP22/00050, RC-0005-2020, FI19/00189, CP18/00042, CD21/00198, IJC2018-037657-I, DOC_01610)
This publication has 35 references indexed in Scilit:
- Atg16l1 is Required for Autophagy in Intestinal Epithelial Cells and Protection of Mice From Salmonella InfectionGastroenterology, 2013
- Mitochondrial morphology in mitophagy and macroautophagyBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 2013
- Fiji: an open-source platform for biological-image analysisNature Methods, 2012
- Oxidized Mitochondrial DNA Activates the NLRP3 Inflammasome during ApoptosisImmunity, 2012
- Induction of dsRNA-activated protein kinase links mitochondrial unfolded protein response to the pathogenesis of intestinal inflammationGut, 2011
- Mitochondrial respiratory chain in the colonic mucosal of patients with ulcerative colitisMolecular and Cellular Biochemistry, 2010
- Circulating mitochondrial DAMPs cause inflammatory responses to injuryNature, 2010
- Bioequivalence study of three ibuprofen formulations after single dose administration in healthy volunteersBMC Pharmacology, 2008
- Cellular Imaging Predictions of Clinical Drug-Induced Liver InjuryToxicological Sciences, 2008
- Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisNature Genetics, 2007