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自噬与精神分裂症:深入探讨神经元细胞内稳态失调如何影响精神分裂症的发病机制

Autophagy and Schizophrenia: A Closer Look at How Dysregulation of Neuronal Cell Homeostasis Influences the Pathogenesis of Schizophrenia.

作者信息

Schneider Jaime L, Miller Ann M, Woesner Mary E

机构信息

Department of Psychiatry & Behavioral Sciences, Albert Einstein College of Medicine, Bronx NY.

Department of Psychiatry & Behavioral Sciences, Albert Einstein College of Medicine, Bronx NY.; Bronx Psychiatric Center, Bronx, NY.

出版信息

Einstein J Biol Med. 2016;31(1-2):34-39. doi: 10.23861/EJBM201631752.

DOI:10.23861/EJBM201631752
PMID:28239307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5321090/
Abstract

Autophagy, the process of degrading intracellular components in lysosomes, plays an important role in the central nervous system by contributing to neuronal homeostasis. Autophagic failure has been linked to neurologic dysfunction and a variety of neurodegenerative diseases. Recent investigation has revealed a novel role for autophagy in the context of mental illness, namely in schizophrenia. This article summarizes the phenomenology, genetics, and structural/histopathological brain abnormalities associated with schizophrenia. We review studies that demonstrate for the first time a connection between autophagy malfunction and schizophrenia. Transcriptional profiling in schizophrenia patients uncovered a dysregulation of autophagy-related genes spatially confined to a specific area of the cortex, Brodmann Area 22, which has been previously implicated in the positive symptoms of schizophrenia. We also discuss the role of autophagy activators in schizophrenia and whether they may be useful adjuvants to the traditional antipsychotic medications currently used as the standard of care. In summary, the field has progressed beyond the basic concept that autophagy impairment predisposes to neurodegeneration, to a mechanistic understanding that loss of autophagy can disrupt neuronal cell biology and predispose to mood disorders, psychotic symptoms, and behavioral change.

摘要

自噬是一种在溶酶体中降解细胞内成分的过程,通过维持神经元内环境稳定在中枢神经系统中发挥重要作用。自噬功能障碍与神经功能障碍及多种神经退行性疾病有关。最近的研究揭示了自噬在精神疾病(即精神分裂症)中的新作用。本文总结了与精神分裂症相关的现象学、遗传学以及大脑结构/组织病理学异常。我们回顾了首次证明自噬功能异常与精神分裂症之间存在关联的研究。对精神分裂症患者的转录谱分析发现,自噬相关基因的失调在空间上局限于大脑皮层的一个特定区域,即布罗德曼22区,该区域此前被认为与精神分裂症的阳性症状有关。我们还讨论了自噬激活剂在精神分裂症中的作用,以及它们是否可能成为目前作为标准治疗药物使用的传统抗精神病药物的有用辅助药物。总之,该领域已经超越了自噬损伤易导致神经退行性变的基本概念,发展到对自噬缺失会破坏神经元细胞生物学并易引发情绪障碍、精神症状和行为改变的机制性理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a37c/5321090/6e5c0a56e131/nihms847197f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a37c/5321090/6e5c0a56e131/nihms847197f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a37c/5321090/6e5c0a56e131/nihms847197f1.jpg

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本文引用的文献

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Autophagy defects at weaning impair complement-dependent synaptic pruning and induce behavior deficits.断奶时自噬缺陷会损害补体依赖性突触修剪,并导致行为缺陷。
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Autophagy-related gene model as a novel risk factor for schizophrenia.自噬相关基因模型作为精神分裂症的一个新的危险因素。
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Chlorpromazine affects autophagy in association with altered Rag GTPase-mTORC1-TFEB signaling.氯丙嗪通过改变Rag GTP酶-mTORC1-TFEB信号传导来影响自噬。
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Antipsychotics Affect Satellite III (1q12) Copy Number Variations in the Cultured Human Skin Fibroblasts.抗精神病药影响培养的人皮肤成纤维细胞中的卫星 III(1q12)拷贝数变异。
Int J Mol Sci. 2023 Jul 10;24(14):11283. doi: 10.3390/ijms241411283.
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自噬在中枢神经系统的生理与病理过程中的作用
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