Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies

Abstract Myocardial ischemia has the highest disease burden among all cardiovascular diseases making it a significant challenge to the global public health. It can result in myocardial cell damage and death due to impaired mitochondrial and endoplasmic reticulum (ER) functions. These two organelles...

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Main Authors: Chen Chen, Guohua Dai, Maoxia Fan, Xingmeng Wang, Kaibin Niu, Wulin Gao
Format: Article
Language:English
Published: BMC 2025-03-01
Series:Journal of Translational Medicine
Subjects:
Online Access:https://doi.org/10.1186/s12967-025-06262-3
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author Chen Chen
Guohua Dai
Maoxia Fan
Xingmeng Wang
Kaibin Niu
Wulin Gao
author_facet Chen Chen
Guohua Dai
Maoxia Fan
Xingmeng Wang
Kaibin Niu
Wulin Gao
author_sort Chen Chen
collection DOAJ
description Abstract Myocardial ischemia has the highest disease burden among all cardiovascular diseases making it a significant challenge to the global public health. It can result in myocardial cell damage and death due to impaired mitochondrial and endoplasmic reticulum (ER) functions. These two organelles are important regulators of cell death. In recent years, research has shifted from isolated studies of individual organelles to a more integrative approach, with a particular focus on their membrane contact sites—Mitochondria-Associated Endoplasmic Reticulum Membranes (MAMs). These dynamic microdomains play a crucial role in regulating material exchange and signal transduction between the endoplasmic reticulum and mitochondria. This review comprehensively describes the intricate structure of MAMs and their multifaceted roles in cellular pathophysiological processes. Particular focus was directed at the far-reaching effects of MAMs in regulating key pathological events including calcium homeostasis, mitochondrial dysfunction, ER stress, oxidative stress, and autophagy in ischemic heart disease (IHD). The potential treatment targets and regulatory mechanisms of MAMs were discussed and summarized, providing novel research directions and treatment approaches for improving myocardial ischemia-related diseases. Graphical Abstract
format Article
id doaj-art-92ffae5e41f440f384eda831689edb14
institution DOAJ
issn 1479-5876
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publishDate 2025-03-01
publisher BMC
record_format Article
series Journal of Translational Medicine
spelling doaj-art-92ffae5e41f440f384eda831689edb142025-08-20T03:05:44ZengBMCJournal of Translational Medicine1479-58762025-03-0123112310.1186/s12967-025-06262-3Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategiesChen Chen0Guohua Dai1Maoxia Fan2Xingmeng Wang3Kaibin Niu4Wulin Gao5First Clinical Medical College, Shandong University of Traditional Chinese MedicineDepartment of Geriatrics, Affiliated Hospital of Shandong University of Traditional Chinese MedicineFirst Clinical Medical College, Shandong University of Traditional Chinese MedicineFirst Clinical Medical College, Shandong University of Traditional Chinese MedicineFirst Clinical Medical College, Shandong University of Traditional Chinese MedicineDepartment of Geriatrics, Affiliated Hospital of Shandong University of Traditional Chinese MedicineAbstract Myocardial ischemia has the highest disease burden among all cardiovascular diseases making it a significant challenge to the global public health. It can result in myocardial cell damage and death due to impaired mitochondrial and endoplasmic reticulum (ER) functions. These two organelles are important regulators of cell death. In recent years, research has shifted from isolated studies of individual organelles to a more integrative approach, with a particular focus on their membrane contact sites—Mitochondria-Associated Endoplasmic Reticulum Membranes (MAMs). These dynamic microdomains play a crucial role in regulating material exchange and signal transduction between the endoplasmic reticulum and mitochondria. This review comprehensively describes the intricate structure of MAMs and their multifaceted roles in cellular pathophysiological processes. Particular focus was directed at the far-reaching effects of MAMs in regulating key pathological events including calcium homeostasis, mitochondrial dysfunction, ER stress, oxidative stress, and autophagy in ischemic heart disease (IHD). The potential treatment targets and regulatory mechanisms of MAMs were discussed and summarized, providing novel research directions and treatment approaches for improving myocardial ischemia-related diseases. Graphical Abstracthttps://doi.org/10.1186/s12967-025-06262-3Mitochondria-associated endoplasmic reticulum membranesMyocardial ischemiaCalcium homeostasisCellular stress
spellingShingle Chen Chen
Guohua Dai
Maoxia Fan
Xingmeng Wang
Kaibin Niu
Wulin Gao
Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies
Journal of Translational Medicine
Mitochondria-associated endoplasmic reticulum membranes
Myocardial ischemia
Calcium homeostasis
Cellular stress
title Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies
title_full Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies
title_fullStr Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies
title_full_unstemmed Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies
title_short Mitochondria-associated endoplasmic reticulum membranes and myocardial ischemia: from molecular mechanisms to therapeutic strategies
title_sort mitochondria associated endoplasmic reticulum membranes and myocardial ischemia from molecular mechanisms to therapeutic strategies
topic Mitochondria-associated endoplasmic reticulum membranes
Myocardial ischemia
Calcium homeostasis
Cellular stress
url https://doi.org/10.1186/s12967-025-06262-3
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