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本文引用的文献

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Autophagic lipid metabolism sustains mTORC1 activity in TSC-deficient neural stem cells.自噬脂质代谢维持 TSC 缺陷性神经干细胞中的 mTORC1 活性。
Nat Metab. 2019 Nov;1(11):1127-1140. doi: 10.1038/s42255-019-0137-5. Epub 2019 Nov 11.
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Cortical Transplantation of Brain-Mimetic Glycosaminoglycan Scaffolds and Neural Progenitor Cells Promotes Vascular Regeneration and Functional Recovery after Ischemic Stroke in Mice.脑仿生糖胺聚糖支架和神经祖细胞的皮质移植促进缺血性卒中后小鼠的血管再生和功能恢复。
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Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localization.肌萎缩侧索硬化症相关蛋白通过调节应激颗粒动态和运动神经元存活蛋白定位来充当融合蛋白毒性的修饰物。
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Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia.22q11.2 缺失综合征和精神分裂症患者诱导多能干细胞源性神经元中的线粒体缺陷。
Transl Psychiatry. 2019 Nov 18;9(1):302. doi: 10.1038/s41398-019-0643-y.
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The application of human pluripotent stem cells to model the neuronal and glial components of neurodevelopmental disorders.人类多能干细胞在神经发育障碍的神经元和神经胶质成分模型中的应用。
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Polygenic risk scores in psychiatry: Will they be useful for clinicians?精神病学中的多基因风险评分:它们对临床医生有用吗?
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Myelin status and oligodendrocyte lineage cells over time after spinal cord injury: What do we know and what still needs to be unwrapped?脊髓损伤后髓鞘状态和少突胶质细胞谱系细胞的时间变化:我们了解什么,还有什么需要揭示?
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Current understandings of the trajectory and emerging correlates of cognitive impairment in bipolar disorder: An overview of evidence.当前对双相情感障碍认知障碍轨迹和新兴相关性的理解:证据概述。
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Imaging Genetics Towards a Refined Diagnosis of Schizophrenia.影像遗传学助力精神分裂症的精准诊断
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干细胞调控作为严重精神障碍和认知障碍的治疗方法

Modulation of Stem Cells as Therapeutics for Severe Mental Disorders and Cognitive Impairments.

作者信息

Zhang Yongbo, Zhao Yingying, Song Xiaopeng, Luo Hua, Sun Jinmei, Han Chunyu, Gu Xiaohuan, Li Jun, Cai Guilan, Zhu Yanbing, Liu Zhandong, Wei Ling, Wei Zheng Zachory

机构信息

Department of Neurology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

Experimental and Translational Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

出版信息

Front Psychiatry. 2020 Apr 30;11:80. doi: 10.3389/fpsyt.2020.00080. eCollection 2020.

DOI:10.3389/fpsyt.2020.00080
PMID:32425815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7205035/
Abstract

Severe mental illnesses (SMI) such as schizophrenia and bipolar disorder affect 2-4% of the world population. Current medications and diagnostic methods for mental illnesses are not satisfying. In animal studies, stem cell therapy is promising for some neuropsychiatric disorders and cognitive/social deficits, not only treating during development (targeting modulation and balancing) but also following neurodegeneration (cell replacement and regenerating support). We believe that novel interventions such as modulation of particular cell populations to develop cell-based treatment can improve cognitive and social functions in SMI. With pathological synaptic/myelin damage, oligodendrocytes seem to play a role. In this review, we have summarized oligodendrogenesis mechanisms and some related calcium signals in neural cells and stem/progenitor cells. The related benefits from endogenous stem/progenitor cells within the brain and exogenous stem cells, including multipotent mesenchymal-derived stromal cells (MSC), fetal neural stem cells (NSC), pluripotent stem cells (PSC), and differentiated progenitors, are discussed. These also include stimulating mechanisms of oligodendrocyte proliferation, maturation, and myelination, responsive to the regenerative effects by both endogenous stem cells and transplanted cells. Among the mechanisms, calcium signaling regulates the neuronal/glial progenitor cell (NPC/GPC)/oligodendrocyte precursor cell (OPC) proliferation, migration, and differentiation, dendrite development, and synaptic plasticity, which are involved in many neuropsychiatric diseases in human. On the basis of numerous protein annotation and protein-protein interaction databases, a total of 119 calcium-dependent/activated proteins that are related to neuropsychiatry in human are summarized in this investigation. One of the advanced methods, the calcium/cation-channel-optogenetics-based stimulation of stem cells and transplanted cells, can take advantage of calcium signaling regulations. Intranasal-to-brain delivery of drugs and stem cells or local delivery with the guidance of brain imaging techniques may provide a unique new approach for treating psychiatric disorders. It is also expected that preconditioning stem cell therapy following precise brain imaging as pathological confirmation has high potential if translated to cell clinic use. Generally, modulable cell transplantation followed by stimulations should provide paracrine protection, synaptic modulation, and myelin repair for the brain in SMI.

摘要

精神分裂症和双相情感障碍等严重精神疾病影响着全球2%至4%的人口。目前针对精神疾病的药物和诊断方法并不令人满意。在动物研究中,干细胞疗法对某些神经精神疾病和认知/社交缺陷具有前景,不仅可在发育过程中进行治疗(靶向调节和平衡),还可在神经退行性变后进行治疗(细胞替代和再生支持)。我们认为,诸如调节特定细胞群以开发基于细胞的治疗方法等新型干预措施,可以改善严重精神疾病患者的认知和社交功能。鉴于存在病理性突触/髓鞘损伤,少突胶质细胞似乎发挥了作用。在本综述中,我们总结了少突胶质细胞生成机制以及神经细胞和干/祖细胞中的一些相关钙信号。讨论了脑内源性干/祖细胞和外源性干细胞(包括多能间充质来源的基质细胞(MSC)、胎儿神经干细胞(NSC)、多能干细胞(PSC)和分化的祖细胞)的相关益处。这些还包括少突胶质细胞增殖、成熟和髓鞘形成的刺激机制,其对内源性干细胞和移植细胞的再生效应均有反应。在这些机制中,钙信号调节神经元/神经胶质祖细胞(NPC/GPC)/少突胶质细胞前体细胞(OPC)的增殖、迁移和分化、树突发育以及突触可塑性,而这些都与人类的许多神经精神疾病有关。基于众多蛋白质注释和蛋白质-蛋白质相互作用数据库,本研究共总结了119种与人类神经精神疾病相关的钙依赖性/激活蛋白。先进方法之一,即基于钙/阳离子通道光遗传学对干细胞和移植细胞进行刺激,可利用钙信号调节。药物和干细胞的鼻内至脑递送或在脑成像技术引导下的局部递送可能为治疗精神疾病提供一种独特的新方法。如果转化为细胞临床应用,预计在精确脑成像作为病理确认后进行预处理干细胞治疗具有很高的潜力。一般来说,可调节的细胞移植后进行刺激应为严重精神疾病患者的大脑提供旁分泌保护、突触调节和髓鞘修复。