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2
Cerebellar demyelination and neurodegeneration associated with mTORC1 hyperactivity may contribute to the developmental onset of autism-like neurobehavioral phenotype in a rat model.小脑脱髓鞘和与 mTORC1 过度活跃相关的神经退行性变可能导致大鼠模型中自闭症样神经行为表型的发育性发作。
Autism Res. 2022 May;15(5):791-805. doi: 10.1002/aur.2688. Epub 2022 Feb 18.
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Myelination Deficits in the Auditory Brainstem of a Mouse Model of Fragile X Syndrome.脆性X综合征小鼠模型听觉脑干中的髓鞘形成缺陷
Front Neurosci. 2021 Nov 11;15:772943. doi: 10.3389/fnins.2021.772943. eCollection 2021.
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Free-floating Immunostaining of Mouse Brains.游离免疫染色的鼠脑。
J Vis Exp. 2021 Oct 7(176). doi: 10.3791/62876.
5
A myelin-related transcriptomic profile is shared by Pitt-Hopkins syndrome models and human autism spectrum disorder.Pitt-Hopkins 综合征模型和人类自闭症谱系障碍共享与髓鞘相关的转录组特征。
Nat Neurosci. 2020 Mar;23(3):375-385. doi: 10.1038/s41593-019-0578-x. Epub 2020 Feb 3.
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Oligodendrocytes in Development, Myelin Generation and Beyond.少突胶质细胞在发育、髓鞘生成及其他方面的作用。
Cells. 2019 Nov 12;8(11):1424. doi: 10.3390/cells8111424.
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Axonal Computations.轴突计算
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8
The Molecular Basis for Remyelination Failure in Multiple Sclerosis.多发性硬化症中髓鞘修复失败的分子基础。
Cells. 2019 Aug 3;8(8):825. doi: 10.3390/cells8080825.
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Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug.神经元中 Gtf2i 的缺失与威廉姆斯综合征有关,可导致行为和髓鞘改变,一种髓鞘修复药物可对此进行挽救。
Nat Neurosci. 2019 May;22(5):700-708. doi: 10.1038/s41593-019-0380-9. Epub 2019 Apr 22.
10
Quantitative analysis of lipid debris accumulation caused by cuprizone induced myelin degradation in different CNS areas.定量分析不同中枢神经系统区域因杯状蛋白诱导髓鞘降解而导致的脂质碎片堆积。
Brain Res Bull. 2018 Mar;137:277-284. doi: 10.1016/j.brainresbull.2018.01.003. Epub 2018 Jan 8.

相干反斯托克斯拉曼光谱(CARS)在脑片髓鞘成像中的应用。

Coherent Anti-Stokes Raman Spectroscopy (CARS) Application for Imaging Myelination in Brain Slices.

机构信息

Department of Integrative Biology, Oklahoma State University;

Department of Physiology and Biophysics, University of Colorado Anschutz.

出版信息

J Vis Exp. 2022 Jul 22(185). doi: 10.3791/64013.

DOI:10.3791/64013
PMID:35938838
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9484306/
Abstract

Coherent anti-Stokes Raman spectroscopy (CARS) is a technique classically employed by chemists and physicists to produce a coherent signal of signature vibrations of molecules. However, these vibrational signatures are also characteristic of molecules within anatomical tissue such as the brain, making it increasingly useful and applicable for Neuroscience applications. For example, CARS can measure lipids by specifically exciting chemical bonds within these molecules, allowing for quantification of different aspects of tissue, such as myelin involved in neurotransmission. In addition, compared to other techniques typically used to quantify myelin, CARS can also be set up to be compatible with immunofluorescent techniques, allowing for co-labeling with other markers such as sodium channels or other components of synaptic transmission. Myelination changes are an inherently important mechanism in demyelinating diseases such as multiple sclerosis or other neurological conditions such as Fragile X Syndrome or autism spectrum disorders is an emerging area of research. In conclusion, CARS can be utilized in innovative ways to answer pressing questions in Neuroscience and provide evidence for underlying mechanisms related to many different neurological conditions.

摘要

相干反斯托克斯拉曼光谱(CARS)是一种化学家和物理学家经典使用的技术,用于产生分子特征振动的相干信号。然而,这些振动特征也是大脑等解剖组织内分子的特征,因此它在神经科学应用中变得越来越有用和适用。例如,CARS 可以通过专门激发这些分子内的化学键来测量脂质,从而可以定量组织的不同方面,如参与神经传递的髓鞘。此外,与通常用于定量髓鞘的其他技术相比,CARS 也可以设置为与免疫荧光技术兼容,从而可以与其他标记物(如钠通道或突触传递的其他成分)进行共标记。髓鞘变化是脱髓鞘疾病(如多发性硬化症)或其他神经状况(如脆性 X 综合征或自闭症谱系障碍)的固有重要机制,是一个新兴的研究领域。总之,CARS 可以以创新的方式用于回答神经科学中的紧迫问题,并为许多不同神经状况的相关潜在机制提供证据。