Mohan A Anjana, Talwar Priti
Apoptosis and Cell Survival Research Laboratory, 412G Pearl Research Park, Department of Biosciences, School of Biosciences and Technology, Vellore Institute of Technology, Vellore, Tamil Nadu, 632014, India.
Cell Mol Biol Lett. 2025 Mar 28;30(1):35. doi: 10.1186/s11658-025-00714-w.
Mitochondria-associated membranes (MAMs) are tethering regions amid the membranes of the endoplasmic reticulum (ER) and mitochondria. They are a lipid raft-like structure occupied by various proteins that facilitates signal transduction between the two organelles. The MAM proteome participates in cellular functions such as calcium (Ca) homeostasis, lipid synthesis, ER stress, inflammation, autophagy, mitophagy, and apoptosis. The human kinome is a superfamily of homologous proteins consisting of 538 kinases. MAM-associated kinases participate in the aforementioned cellular functions and act as cell fate executors. Studies have proved the dysregulated kinase interactions in MAM as an etiology for various diseases including cancer, diabetes mellitus, neurodegenerative diseases, cardiovascular diseases (CVDs), and obesity. Several small kinase inhibitory molecules have been well explored as promising drug candidates in clinical trials with an accelerating impact in the field of precision medicine. This review narrates the physiological actions, pathophysiology, and therapeutic potential of MAM-associated kinases with recent updates in the field.
线粒体相关膜(MAMs)是内质网(ER)和线粒体膜之间的连接区域。它们是一种类似脂筏的结构,被各种蛋白质占据,有助于两个细胞器之间的信号转导。MAM蛋白质组参与细胞功能,如钙(Ca)稳态、脂质合成、内质网应激、炎症、自噬、线粒体自噬和细胞凋亡。人类激酶组是一个由538种激酶组成的同源蛋白质超家族。与MAM相关的激酶参与上述细胞功能,并作为细胞命运执行者。研究已证明MAM中激酶相互作用失调是包括癌症、糖尿病、神经退行性疾病、心血管疾病(CVDs)和肥胖症在内的各种疾病的病因。几种小激酶抑制分子已在临床试验中作为有前景的候选药物得到充分探索,对精准医学领域产生了加速影响。这篇综述叙述了与MAM相关激酶的生理作用、病理生理学和治疗潜力,并介绍了该领域的最新进展。