Mitoregulin supports mitochondrial membrane integrity and protects against cardiac ischaemia–reperfusion injury
Year: 2026
Type: article
Abstract: AIMS: We and others discovered a highly conserved mitochondrial transmembrane microprotein, named Mitoregulin (Mtln), that supports lipid metabolism. We reported that Mtln strongly binds cardiolipin (CL), increases mitochondrial respiration and Ca2+ retention capacities, and reduces reactive oxygen species (ROS). Here, we extend our observation of Mtln-CL binding and examine Mtln influence on cristae structure and mitochondrial membrane integrity during stress. METHODS AND RESULTS: We demonstrate that mitochondria from constitutive- and inducible Mtln-knockout (KO) mice are susceptible to membrane freeze-damage and that this can be rescued by acute Mtln re-expression. In mitochondrial-simulated lipid monolayers, we show that synthetic Mtln decreases lipid packing and monolayer elasticity. Lipidomics revealed that Mtln-KO heart tissues show broad decreases in 22:6-containing lipids and increased cardiolipin damage/remodelling. Finally, we demonstrate that Mtln-KO mice suffer worse myocardial ischaemia-reperfusion injury, hinting at a translationally relevant role for Mtln in cardioprotection. CONCLUSION: Our work supports a model in which Mtln binds cardiolipin and stabilizes mitochondrial membranes to broadly influence diverse mitochondrial functions, including lipid metabolism, while also protecting against stress.
Source: Cardiovascular Research
DOI: 10.1093/cvr/cvag011
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $5,329
Funders: American Heart Association, University of Texas Southwestern Medical Center, National Institutes of Health, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: G1842406475, The physiologic and genomic relevance of mitoregulin in ischemic heart failure, Funds to acquire a JEOL JSM-7401F FESEM, Predoctoral Training in the Pharmacological Sciences, G766600706, Investigating a novel NaV1.5 N-terminal microprotein arising from alternative polyadenylation of SCN5A, Nutrition Obesity Research Center (NORC), Basic and Translational Studies in Redox Regulation of Cardiovascular Physiology and Disease
OpenAlex ID: W7124972543
