中国神经再生研究(英文版) ›› 2026, Vol. 21 ›› Issue (10): 4745-4757.doi: 10.4103/NRR.NRR-D-25-00857

• 综述:退行性病与再生 • 上一篇    下一篇

线粒体相关内质网膜及钙离子交换:衰老与神经退行性疾病研究的新方向

  

  • 出版日期:2026-10-15 发布日期:2026-06-12
  • 基金资助:
    国家自然科学基金(82374580)和首都卫生改善与研究专项资金(2022-2 2233)

Mitochondria-associated endoplasmic reticulum membranes and calcium ion exchange: A novel direction for aging and neurodegenerative diseases

Yuxuan Yang1, Mengjie Chen1, Lingling Ding1, *, Jiaxi Liu1, Jiansheng Luo2, Ruyu Yan1, Jiaqi Ning1, Siyi Xie1, Xiang Li3, Zhihao Ren1, Ruiling Zhou1, Zhuoya Chen1   

  1. 1School of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China; 
    2Characteristic Medical Center of Chinese People’s Armed Police Force, Tianjin, China
  • Online:2026-10-15 Published:2026-06-12
  • Contact: Lingling Ding, MD, dinglingling301@126.com.
  • Supported by:
    This work was supported in part by the National Natural Science Foundation of China, No. 82374580; Capital Funds for Health Improvement and Research, No. 2022-2 2233 (both to LD).

摘要:

线粒体相关内质网膜作为关键的信号枢纽,介导内质网与线粒体之间的跨细胞器通信,特别是在钙离子交换中发挥重要作用,这一动态界面调控着生物能量代谢、凋亡、自噬和应激反应等关键细胞过程。线粒体相关内质网膜相关钙离子转运的失调会破坏细胞内稳态,导致线粒体功能障碍、氧化应激和神经元死亡,这些是衰老及神经退行性疾病的标志。文章着重探讨了线粒体相关内质网膜内蛋白复合物的功能及其在衰老及神经退行性疾病中由线粒体相关内质网膜调控的钙离子信号通路的病理机制,特别强调钙离子转运相关结构的改变是多种神经退行性疾病共有的机制。在阿尔茨海默病中,线粒体相关内质网膜呈现高活性状态,促进β-淀粉样蛋白的生成并增强内质网向线粒体的钙离子流,而在帕金森病和肌萎缩侧索硬化症中,线粒体相关内质网膜活性降低,导致线粒体钙离子缓冲能力下降,加剧兴奋性毒性。线粒体相关内质网膜驻留蛋白在各类神经退行性疾病中均出现紊乱,导致内质网-线粒体通信异常。最新研究表明,线粒体相关内质网膜在疾病进展中具有双向作用,补偿机制常会加重病理进程。针对线粒体相关内质网膜完整性的治疗策略有望缓解神经退行性病变。因此,线粒体相关内质网膜介导的钙离子交换在衰老及神经退行性疾病中扮演关键角色,是极具潜力的治疗靶点。


https://orcid.org/0000-0002-2125-8452 (Lingling Ding)

关键词: 衰老, 阿尔茨海默病, 肌萎缩侧索硬化症, 钙离子通道, 额颞叶痴呆, 线粒体相关内质网膜, 多发性硬化症, 神经退行性疾病, 帕金森病, 程序性细胞死亡

Abstract:

Mitochondria-associated endoplasmic reticulum membranes serve as crucial signaling hubs mediating communication between the endoplasmic reticulum and mitochondria, and play a central role in calcium ion exchange. This dynamic interface regulates key cellular processes including bioenergetic metabolism, apoptosis, autophagy, and stress responses. Dysregulation of calcium transport associated with mitochondria-associated endoplasmic reticulum membranes can disrupt intracellular homeostasis, leading to mitochondrial dysfunction, oxidative stress, and neuronal death, which are hallmarks of aging and neurodegenerative diseases. This review systematically examines the functions of protein complexes within mitochondria-associated endoplasmic reticulum membranes and the pathogenic mechanisms of calcium signaling regulated by these membranes in neurodegenerative disorders. It places particular emphasis on structural alterations in calcium ion transport machinery as a common mechanism underlying various neurodegenerative diseases. In Alzheimer’s disease, mitochondria-associated endoplasmic reticulum membranes exhibit a hyperactive state, promoting the generation of amyloid-β and enhancing calcium ion flux from the endoplasmic reticulum to the mitochondria. In contrast, in Parkinson’s disease and amyotrophic lateral sclerosis, the activity of mitochondria-associated endoplasmic reticulum membranes is reduced, leading to a decline in mitochondrial calcium ion buffering capacity and exacerbating excitotoxicity. Proteins residing in mitochondria-associated endoplasmic reticulum membranes are disrupted across various neurodegenerative diseases, resulting in abnormal communication between the endoplasmic reticulum and mitochondria. Recent studies indicate that mitochondria-associated endoplasmic reticulum membranes play a bidirectional role in disease progression, and compensatory mechanisms often exacerbate the pathological process. Therapeutic strategies aimed at preserving the integrity of mitochondria-associated endoplasmic reticulum membranes hold promise for alleviating neurodegenerative damage. Therefore, calcium ion exchange mediated by mitochondria-associated endoplasmic reticulum membranes plays a key role in aging and neurodegenerative diseases, making it a highly promising therapeutic target.

Key words: aging, Alzheimer’s disease, amyotrophic lateral sclerosis, calcium channels, frontotemporal dementia, mitochondria-associated endoplasmic reticulum membranes, multiple sclerosis, neurodegenerative diseases, Parkinson’s disease, programmed cell death