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在早期发育过程中描绘神经元形态的靶向方法。

Targeted approaches to delineate neuronal morphology during early development.

作者信息

Liu Bimin, Li Yuxiao, Ren Miao, Li Xiangning

机构信息

State Key Laboratory of Digital Medical Engineering, School of Biomedical Engineering, Hainan University, Haikou, China.

Key Laboratory of Biomedical Engineering of Hainan Province, School of Biomedical Engineering, Hainan University, Haikou, China.

出版信息

Front Cell Neurosci. 2023 Oct 3;17:1259360. doi: 10.3389/fncel.2023.1259360. eCollection 2023.

DOI:10.3389/fncel.2023.1259360
PMID:37854514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10579594/
Abstract

Understanding the developmental changes that affect neurons is a key step in exploring the assembly and maturation of neural circuits in the brain. For decades, researchers have used a number of labeling techniques to visualize neuronal morphology at different stages of development. However, the efficiency and accuracy of neuronal labeling technologies are limited by the complexity and fragility of neonatal brains. In this review, we illustrate the various labeling techniques utilized for examining the neurogenesis and morphological changes occurring during the early stages of development. We compare the advantages and limitations of each technique from different aspects. Then, we highlight the gaps remaining in our understanding of the structure of neurons in the neonatal mouse brain.

摘要

了解影响神经元的发育变化是探索大脑神经回路组装和成熟的关键一步。几十年来,研究人员使用了多种标记技术来观察神经元在不同发育阶段的形态。然而,神经元标记技术的效率和准确性受到新生大脑复杂性和脆弱性的限制。在这篇综述中,我们阐述了用于研究发育早期神经发生和形态变化的各种标记技术。我们从不同方面比较了每种技术的优缺点。然后,我们强调了在理解新生小鼠大脑神经元结构方面仍存在的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822d/10579594/00d229836295/fncel-17-1259360-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822d/10579594/a02789b33687/fncel-17-1259360-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822d/10579594/fa357bf4019c/fncel-17-1259360-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822d/10579594/00d229836295/fncel-17-1259360-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822d/10579594/a02789b33687/fncel-17-1259360-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822d/10579594/fa357bf4019c/fncel-17-1259360-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/822d/10579594/00d229836295/fncel-17-1259360-g003.jpg

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本文引用的文献

1
Estimates of total neuron number show that neonatal ethanol causes immediate and lasting neuron loss in cortical and subcortical areas.对神经元总数的估计表明,新生儿接触乙醇会导致皮质和皮质下区域立即且持久的神经元损失。
Front Neurosci. 2023 May 2;17:1186529. doi: 10.3389/fnins.2023.1186529. eCollection 2023.
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Single-Cell Labeling Strategies to Dissect Neuronal Structures and Local Functions.用于剖析神经元结构和局部功能的单细胞标记策略。
Biology (Basel). 2023 Feb 16;12(2):321. doi: 10.3390/biology12020321.
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模式化 cPCDH 表达调控新皮层的精细组织。
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Acetylcholine deficiency disrupts extratelencephalic projection neurons in the prefrontal cortex in a mouse model of Alzheimer's disease.乙酰胆碱缺乏会破坏阿尔茨海默病小鼠模型前额叶皮层的外端脑投射神经元。
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Plastic embedding for precise imaging of large-scale biological tissues labeled with multiple fluorescent dyes and proteins.用于对用多种荧光染料和蛋白质标记的大规模生物组织进行精确成像的塑料包埋。
Biomed Opt Express. 2021 Oct 6;12(11):6730-6745. doi: 10.1364/BOE.435120. eCollection 2021 Nov 1.
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Architectures of neuronal circuits.神经元回路的结构。
Science. 2021 Sep 3;373(6559):eabg7285. doi: 10.1126/science.abg7285.
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Retrograde fluorogold labeling of retinal ganglion cells in neonatal mice.新生小鼠视网膜神经节细胞的逆行荧光金标记
Ann Transl Med. 2021 May;9(10):878. doi: 10.21037/atm-21-2022.
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