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本文引用的文献

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Progressive multiple sclerosis: from pathogenic mechanisms to treatment.进行性多发性硬化症:从发病机制到治疗。
Brain. 2017 Mar 1;140(3):527-546. doi: 10.1093/brain/aww258.
2
The dual S1PR1/S1PR5 drug BAF312 (Siponimod) attenuates demyelination in organotypic slice cultures.双重S1PR1/S1PR5药物BAF312(西尼莫德)可减轻器官型脑片培养中的脱髓鞘现象。
J Neuroinflammation. 2016 Feb 8;13:31. doi: 10.1186/s12974-016-0494-x.
3
Microglial brain region-dependent diversity and selective regional sensitivities to aging.小胶质细胞脑区依赖性多样性及对衰老的选择性区域敏感性。
Nat Neurosci. 2016 Mar;19(3):504-16. doi: 10.1038/nn.4222. Epub 2016 Jan 18.
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Therapeutic Advances and Future Prospects in Progressive Forms of Multiple Sclerosis.进展性多发性硬化症的治疗进展与未来前景。
Neurotherapeutics. 2016 Jan;13(1):58-69. doi: 10.1007/s13311-015-0409-z.
5
Galactosylsphingosine (psychosine)-induced demyelination is attenuated by sphingosine 1-phosphate signalling.半乳糖基鞘氨醇(精神鞘氨醇)诱导的脱髓鞘作用因1-磷酸鞘氨醇信号传导而减弱。
J Cell Sci. 2015 Nov 1;128(21):3878-87. doi: 10.1242/jcs.169342. Epub 2015 Sep 10.
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Organotypic brain slice cultures: A review.器官型脑片培养:综述
Neuroscience. 2015 Oct 1;305:86-98. doi: 10.1016/j.neuroscience.2015.07.086. Epub 2015 Aug 5.
7
Organotypic Hippocampal Slices as Models for Stroke and Traumatic Brain Injury.器官型海马切片作为中风和创伤性脑损伤的模型
Mol Neurobiol. 2016 Aug;53(6):4226-4237. doi: 10.1007/s12035-015-9362-4. Epub 2015 Jul 30.
8
S100B as a Potential Biomarker and Therapeutic Target in Multiple Sclerosis.S100B作为多发性硬化症的潜在生物标志物和治疗靶点。
Mol Neurobiol. 2016 Aug;53(6):3976-3991. doi: 10.1007/s12035-015-9336-6. Epub 2015 Jul 17.
9
From mishap to model: The origins and utility of experimental autoimmune encephalomyelitis.从意外发现到模型:实验性自身免疫性脑脊髓炎的起源与应用
Biomed J. 2015 May-Jun;38(3):177-80. doi: 10.4103/2319-4170.158498.
10
N-3 polyunsaturated fatty acids in animal models with neuroinflammation: An update.神经炎症动物模型中的n-3多不饱和脂肪酸:最新进展
Eur J Pharmacol. 2016 Aug 15;785:187-206. doi: 10.1016/j.ejphar.2015.05.045. Epub 2015 May 30.

成年中枢神经系统的器官型培养:体外研究脱髓鞘和髓鞘再生的新模型。

Organotypic Cultures from the Adult CNS: A Novel Model to Study Demyelination and Remyelination Ex Vivo.

机构信息

Laboratory of Molecular Cell Biology, College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK, Canada.

Neuroscience Research Cluster, University of Saskatchewan, Saskatoon, SK, Canada.

出版信息

Cell Mol Neurobiol. 2018 Jan;38(1):317-328. doi: 10.1007/s10571-017-0529-6. Epub 2017 Aug 9.

DOI:10.1007/s10571-017-0529-6
PMID:28795301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11481926/
Abstract

Experimental models of multiple sclerosis (MS) have significantly advanced our understanding of pathophysiology and therapeutic interventions. Although in vivo rodent models are considered to most closely represent the complex cellular and molecular disease states of the human central nervous system (CNS), these can be costly to maintain and require long timelines. Organotypic slice cultures maintain the cytotypic organization observed in the intact CNS, yet provide many of the experimental advantages of in vitro cell culture models. Cerebellar organotypic cultures have proven useful for studying myelination and remyelination, but this model has only been established using early postnatal tissue. This young brain tissue allows for neuro development ex vivo to mimic the 'mature' CNS; however, there are many differences between postnatal and adult organotypic cultures. This may be particularly relevant to MS, as a major barrier to myelin regeneration is age. This paper describes a modified protocol to study demyelination and remyelination in adult cerebellar tissue, which has been used to demonstrate neuroprotection with omega-3 fatty acids. Thus, adult cerebellar organotypic cultures provide a novel ex vivo platform for screening potential therapies in myelin degeneration and repair.

摘要

实验性多发性硬化症 (MS) 模型极大地促进了我们对病理生理学和治疗干预的理解。尽管体内啮齿动物模型被认为最能代表人类中枢神经系统 (CNS) 的复杂细胞和分子疾病状态,但这些模型维持成本高,需要很长的时间。器官型切片培养保持了完整 CNS 中观察到的细胞表型组织,但提供了许多体外细胞培养模型的实验优势。小脑器官型培养已被证明可用于研究髓鞘形成和再髓鞘化,但这种模型仅使用早期产后组织建立。这种年轻的脑组织允许体外神经发育来模拟“成熟”的 CNS;然而,产后和成年器官型培养之间存在许多差异。这在多发性硬化症中可能特别重要,因为髓鞘再生的一个主要障碍是年龄。本文描述了一种改良的方案,用于研究成年小脑组织中的脱髓鞘和再髓鞘化,该方案已被用于证明 ω-3 脂肪酸的神经保护作用。因此,成年小脑器官型培养为筛选髓鞘退化和修复的潜在治疗方法提供了一个新的体外平台。