Experimental Cell Research, Journal Year: 2024, Volume and Issue: unknown, P. 114380 - 114380
Published: Dec. 1, 2024
Language: Английский
Experimental Cell Research, Journal Year: 2024, Volume and Issue: unknown, P. 114380 - 114380
Published: Dec. 1, 2024
Language: Английский
Biomedicine & Pharmacotherapy, Journal Year: 2025, Volume and Issue: 183, P. 117838 - 117838
Published: Jan. 11, 2025
Language: Английский
Citations
0Phytomedicine, Journal Year: 2025, Volume and Issue: 138, P. 156411 - 156411
Published: Jan. 21, 2025
Language: Английский
Citations
0Biomedicine & Pharmacotherapy, Journal Year: 2025, Volume and Issue: 183, P. 117840 - 117840
Published: Jan. 21, 2025
Language: Английский
Citations
0Cellular Signalling, Journal Year: 2025, Volume and Issue: 130, P. 111663 - 111663
Published: Feb. 15, 2025
Language: Английский
Citations
0Cellular Signalling, Journal Year: 2025, Volume and Issue: 129, P. 111662 - 111662
Published: Feb. 16, 2025
Language: Английский
Citations
0Journal of Translational Medicine, Journal Year: 2025, Volume and Issue: 23(1)
Published: March 6, 2025
Myocardial ischemia has the highest disease burden among all cardiovascular diseases making it a significant challenge to global public health. It can result in myocardial cell damage and death due impaired mitochondrial endoplasmic reticulum (ER) functions. These two organelles are important regulators of death. In recent years, research shifted from isolated studies individual more integrative approach, with particular focus on their membrane contact sites-Mitochondria-Associated Endoplasmic Reticulum Membranes (MAMs). dynamic microdomains play crucial role regulating material exchange signal transduction between mitochondria. This review comprehensively describes intricate structure MAMs multifaceted roles cellular pathophysiological processes. Particular was directed at far-reaching effects key pathological events including calcium homeostasis, dysfunction, ER stress, oxidative autophagy ischemic heart (IHD). The potential treatment targets regulatory mechanisms were discussed summarized, providing novel directions approaches for improving ischemia-related diseases.
Language: Английский
Citations
0European Journal of Pharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 177477 - 177477
Published: March 1, 2025
Language: Английский
Citations
0Cellular Signalling, Journal Year: 2025, Volume and Issue: unknown, P. 111734 - 111734
Published: March 1, 2025
Language: Английский
Citations
0Experimental Cell Research, Journal Year: 2025, Volume and Issue: unknown, P. 114537 - 114537
Published: March 1, 2025
Language: Английский
Citations
0Cellular & Molecular Biology Letters, Journal Year: 2025, Volume and Issue: 30(1)
Published: March 28, 2025
Abstract Mitochondria-associated membranes (MAMs) are tethering regions amid the of endoplasmic reticulum (ER) and mitochondria. They a lipid raft-like structure occupied by various proteins that facilitates signal transduction between two organelles. The MAM proteome participates in cellular functions such as calcium (Ca 2+ ) homeostasis, synthesis, ER stress, inflammation, autophagy, mitophagy, apoptosis. human kinome is superfamily homologous consisting 538 kinases. MAM-associated kinases participate aforementioned act cell fate executors. Studies have proved dysregulated kinase interactions an etiology for diseases including cancer, diabetes mellitus, neurodegenerative diseases, cardiovascular (CVDs), obesity. Several small inhibitory molecules been well explored promising drug candidates clinical trials with accelerating impact field precision medicine. This review narrates physiological actions, pathophysiology, therapeutic potential recent updates field. Graphical
Language: Английский
Citations
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