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人脑类器官模型在人类神经精神连接疾病研究中的现状和未来

Present and Future Modeling of Human Psychiatric Connectopathies With Brain Organoids.

机构信息

Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California.

Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California.

出版信息

Biol Psychiatry. 2023 Apr 1;93(7):606-615. doi: 10.1016/j.biopsych.2022.12.017. Epub 2022 Dec 23.

DOI:10.1016/j.biopsych.2022.12.017
PMID:36759258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11229385/
Abstract

Brain organoids derived from human pluripotent stem cells are emerging as a powerful tool to model cellular aspects of neuropsychiatric disorders, including alterations in cell proliferation, differentiation, migration, and lineage trajectory. To date, most contributions in the field have focused on modeling cellular impairment of the cerebral cortex, with few studies probing dysfunction in local network connectivity. However, it is increasingly more apparent that these psychiatric disorders are connectopathies involving multiple brain structures and the connections between them. Therefore, the lack of reproducible anatomical features in these 3-dimensional cultures represents a major bottleneck for effectively modeling brain connectivity at the micro(cellular) level and at the macroscale level between brain regions. In this perspective, we review the use of current organoid protocols to model neuropsychiatric disorders with a specific emphasis on the potential and limitations of the current strategies to model impairments in functional connectivity. Finally, we discuss the importance of adopting interdisciplinary strategies to establish next-generation, multiregional organoids that can model, with higher fidelity, the dysfunction in the development and functionality of long-range connections within the brain of patients affected by psychiatric disorders.

摘要

人脑类器官源自人类多能干细胞,现已成为神经精神疾病细胞方面建模的有力工具,包括细胞增殖、分化、迁移和谱系轨迹的改变。迄今为止,该领域的大多数研究都集中在模拟大脑皮层的细胞功能障碍上,很少有研究探究局部网络连接的功能障碍。然而,越来越明显的是,这些精神疾病是涉及多个脑结构及其之间连接的连接病。因此,这些 3 维培养物中缺乏可重复的解剖特征,是在微(细胞)水平和大脑区域之间的宏观水平上有效模拟脑连接的主要瓶颈。在这方面,我们回顾了当前使用类器官技术来模拟神经精神疾病的方法,特别强调了当前用于模拟功能连接障碍的策略的潜力和局限性。最后,我们讨论了采用跨学科策略来建立新一代、多区域类器官的重要性,这些类器官可以更准确地模拟受精神疾病影响的患者大脑中长程连接的发育和功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4862/11229385/76db1584c13b/nihms-2005885-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4862/11229385/66039259ebe5/nihms-2005885-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4862/11229385/76db1584c13b/nihms-2005885-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4862/11229385/66039259ebe5/nihms-2005885-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4862/11229385/76db1584c13b/nihms-2005885-f0002.jpg

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本文引用的文献

1
Complex activity and short-term plasticity of human cerebral organoids reciprocally connected with axons.人类脑类器官的复杂活动和短期可塑性与轴突相互连接。
Nat Commun. 2024 Apr 10;15(1):2945. doi: 10.1038/s41467-024-46787-7.
2
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex.细胞命运决策图揭示了人类发育新皮层中大量绕过中间祖细胞的直接神经发生。
Nat Cell Biol. 2024 May;26(5):698-709. doi: 10.1038/s41556-024-01393-z. Epub 2024 Mar 28.
3
An epigenetic barrier sets the timing of human neuronal maturation.表观遗传屏障决定了人类神经元成熟的时间。
Nature. 2024 Feb;626(8000):881-890. doi: 10.1038/s41586-023-06984-8. Epub 2024 Jan 31.
4
Modeling idiopathic autism in forebrain organoids reveals an imbalance of excitatory cortical neuron subtypes during early neurogenesis.在大脑器官样体中模拟特发性自闭症揭示了早期神经发生过程中兴奋性皮质神经元亚型的失衡。
Nat Neurosci. 2023 Sep;26(9):1505-1515. doi: 10.1038/s41593-023-01399-0. Epub 2023 Aug 10.
5
Benchmarking brain organoid recapitulation of fetal corticogenesis.脑类器官对胎儿皮质发生的重演性基准测试。
Transl Psychiatry. 2022 Dec 20;12(1):520. doi: 10.1038/s41398-022-02279-0.
6
Ascertaining cells' synaptic connections and RNA expression simultaneously with barcoded rabies virus libraries.利用带有条形码的狂犬病毒文库同时确定细胞的突触连接和 RNA 表达。
Nat Commun. 2022 Nov 16;13(1):6993. doi: 10.1038/s41467-022-34334-1.
7
Maturation and circuit integration of transplanted human cortical organoids.移植的人类皮质类器官的成熟和回路整合。
Nature. 2022 Oct;610(7931):319-326. doi: 10.1038/s41586-022-05277-w. Epub 2022 Oct 12.
8
CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories.CHD8 杂合性不足将自闭症与兴奋性和抑制性轨迹的短暂改变联系起来。
Cell Rep. 2022 Apr 5;39(1):110615. doi: 10.1016/j.celrep.2022.110615.
9
Autism genes converge on asynchronous development of shared neuron classes.自闭症基因集中于共享神经元类别的异步发育。
Nature. 2022 Feb;602(7896):268-273. doi: 10.1038/s41586-021-04358-6. Epub 2022 Feb 2.
10
Dissecting the molecular basis of human interneuron migration in forebrain assembloids from Timothy syndrome.剖析蒂莫西综合征患者前脑类器官中人类中间神经元迁移的分子基础。
Cell Stem Cell. 2022 Feb 3;29(2):248-264.e7. doi: 10.1016/j.stem.2021.11.011. Epub 2022 Jan 5.