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线粒体功能障碍和有缺陷的线粒体自噬在自闭症谱系障碍中的关键作用。

Critical role of dysfunctional mitochondria and defective mitophagy in autism spectrum disorders.

机构信息

Hengyang Key Laboratory of Neurodegeneration and Cognitive Impairment & Institute of Neuroscience, Hengyang Medical College, University of South China, Hengyang, Hunan, 421001, People's Republic of China; Lhasa Guangsheng Hospital, Lhasa, People's Republic of China.

Hengyang Key Laboratory of Neurodegeneration and Cognitive Impairment & Institute of Neuroscience, Hengyang Medical College, University of South China, Hengyang, Hunan, 421001, People's Republic of China; Lhasa Guangsheng Hospital, Lhasa, People's Republic of China.

出版信息

Brain Res Bull. 2021 Mar;168:138-145. doi: 10.1016/j.brainresbull.2020.12.022. Epub 2021 Jan 2.

Abstract

Autism spectrum disorders (ASDs) are a group of complex neurodevelopmental disorders, including autistic disorder, Asperger's syndrome, pervasive developmental disorder and childhood disintegrative disorder. Mitochondria not only provide neurons with energy in the form of ATP to sustain neuron growth, proliferation and neurodevelopment, but also regulate neuron apoptosis, intracellular calcium ion (Ca) homeostasis, and reactive oxygen species (ROS) clearance. Due to their postmitotic state and high energy-demanded feature, neurons are particularly prone to mitophagy and mitochondrial disfunction. Mitophagy, a selective autophagy, is critical for sustaining mitochondrial turnover and quality control via eliminating unwanted and dysfunctional mitochondria in neurons. Dysfunctional mitochondria and dysregulated mitophagy have been closely associated with the onset of ASDs. In this review, we summarize the mechanism of mitophagy and its role in neurons, and the consequence of mitophagy dysfunction in ASDs. Deeper appreciation of the role of mitophagy in ASDs pathology is required for developing new therapeutic approaches.

摘要

自闭症谱系障碍(ASD)是一组复杂的神经发育障碍,包括自闭症、阿斯伯格综合征、广泛性发育障碍和儿童瓦解性障碍。线粒体不仅以 ATP 的形式为神经元提供能量来维持神经元的生长、增殖和神经发育,还调节神经元凋亡、细胞内钙离子(Ca)稳态和活性氧(ROS)清除。由于神经元处于有丝分裂后状态且能量需求高,因此特别容易发生线粒体自噬和线粒体功能障碍。线粒体自噬是一种选择性自噬,通过清除神经元中不需要的和功能失调的线粒体,对于维持线粒体的周转率和质量控制至关重要。功能失调的线粒体和失调的线粒体自噬与 ASD 的发病密切相关。在这篇综述中,我们总结了线粒体自噬的机制及其在神经元中的作用,以及线粒体自噬功能障碍在 ASD 中的后果。为了开发新的治疗方法,需要更深入地了解线粒体自噬在 ASD 病理学中的作用。

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