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本文引用的文献

1
An inducible glycogen synthase-1 knockout halts but does not reverse Lafora disease progression in mice.诱导型糖原合酶-1 敲除可阻止但不能逆转小鼠的拉佛拉病进展。
J Biol Chem. 2021 Jan-Jun;296:100150. doi: 10.1074/jbc.RA120.015773. Epub 2020 Dec 10.
2
Suppression of glycogen synthesis as a treatment for Lafora disease: Establishing the window of opportunity.抑制糖原合成作为拉福拉病的治疗方法:确定治疗时机。
Neurobiol Dis. 2021 Jan;147:105173. doi: 10.1016/j.nbd.2020.105173. Epub 2020 Nov 7.
3
Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora disease.PPP1R3D 缺失优先抑制致命性癫痫性 Lafora 病小鼠模型中的神经元和心脏 Lafora 体形成。
J Neurochem. 2021 Jun;157(6):1897-1910. doi: 10.1111/jnc.15176. Epub 2020 Oct 10.
4
Antisense oligonucleotides increase expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome.反义寡核苷酸可增加表达,减少癫痫发作和 Dravet 综合征小鼠模型中 SUDEP 的发生率。
Sci Transl Med. 2020 Aug 26;12(558). doi: 10.1126/scitranslmed.aaz6100.
5
Reactive Glia-Derived Neuroinflammation: a Novel Hallmark in Lafora Progressive Myoclonus Epilepsy That Progresses with Age.反应性神经胶质衍生的神经炎症:在拉福拉进行性肌阵挛性癫痫中随着年龄增长而进展的新特征。
Mol Neurobiol. 2020 Mar;57(3):1607-1621. doi: 10.1007/s12035-019-01842-z. Epub 2019 Dec 5.
6
Skeletal Muscle Glycogen Chain Length Correlates with Insolubility in Mouse Models of Polyglucosan-Associated Neurodegenerative Diseases.骨骼肌糖原链长与多聚糖相关神经退行性疾病小鼠模型中的不溶性相关。
Cell Rep. 2019 Apr 30;27(5):1334-1344.e6. doi: 10.1016/j.celrep.2019.04.017.
7
Astrocytes and neurons produce distinct types of polyglucosan bodies in Lafora disease.Lafora 病中星形胶质细胞和神经元产生不同类型的多聚葡聚糖体。
Glia. 2018 Oct;66(10):2094-2107. doi: 10.1002/glia.23463. Epub 2018 Aug 26.
8
Lafora disease - from pathogenesis to treatment strategies.拉佛拉病——从发病机制到治疗策略。
Nat Rev Neurol. 2018 Oct;14(10):606-617. doi: 10.1038/s41582-018-0057-0.
9
Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy.依库珠单抗治疗晚发性脊髓性肌萎缩症的疗效观察:一项随机、双盲、安慰剂对照 3 期试验
N Engl J Med. 2018 Feb 15;378(7):625-635. doi: 10.1056/NEJMoa1710504.
10
Astrocytes: new players in progressive myoclonus epilepsy of Lafora type.星形胶质细胞:Lafora 型进行性肌阵挛癫痫的新角色。
Hum Mol Genet. 2018 Apr 1;27(7):1290-1300. doi: 10.1093/hmg/ddy044.

Gys1 反义疗法可挽救小鼠拉福拉病的神经病理学基础。

Gys1 antisense therapy rescues neuropathological bases of murine Lafora disease.

机构信息

Program in Genetics and Genome Biology, The Hospital for Sick Children Research Institute, Toronto, ON M5G 0A4, Canada.

Division of Neurology, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

出版信息

Brain. 2021 Nov 29;144(10):2985-2993. doi: 10.1093/brain/awab194.

DOI:10.1093/brain/awab194
PMID:33993268
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8634080/
Abstract

Lafora disease is a fatal progressive myoclonus epilepsy. At root, it is due to constant acquisition of branches that are too long in a subgroup of glycogen molecules, leading them to precipitate and accumulate into Lafora bodies, which drive a neuroinflammatory response and neurodegeneration. As a potential therapy, we aimed to downregulate glycogen synthase, the enzyme responsible for glycogen branch elongation, in mouse models of the disease. We synthesized an antisense oligonucleotide (Gys1-ASO) that targets the mRNA of the brain-expressed glycogen synthase 1 gene (Gys1). We administered Gys1-ASO by intracerebroventricular injection and analysed the pathological hallmarks of Lafora disease, namely glycogen accumulation, Lafora body formation, and neuroinflammation. Gys1-ASO prevented Lafora body formation in young mice that had not yet formed them. In older mice that already exhibited Lafora bodies, Gys1-ASO inhibited further accumulation, markedly preventing large Lafora bodies characteristic of advanced disease. Inhibition of Lafora body formation was associated with prevention of astrogliosis and strong trends towards correction of dysregulated expression of disease immune and neuroinflammatory markers. Lafora disease manifests gradually in previously healthy teenagers. Our work provides proof of principle that an antisense oligonucleotide targeting the GYS1 mRNA could prevent, and halt progression of, this catastrophic epilepsy.

摘要

拉佛拉病是一种致命的进行性肌阵挛性癫痫。从根本上说,它是由于糖元分子亚群中不断形成过长的分支,导致它们沉淀并聚积形成拉佛拉体,从而引发神经炎症反应和神经退行性变。作为一种潜在的治疗方法,我们旨在下调疾病小鼠模型中负责糖原分支伸长的糖原合酶的表达。我们合成了一种针对脑表达的糖原合酶 1 基因(Gys1)mRNA 的反义寡核苷酸(Gys1-ASO)。我们通过脑室内注射给予 Gys1-ASO,并分析拉佛拉病的病理特征,即糖原积累、拉佛拉体形成和神经炎症。Gys1-ASO 可预防尚未形成拉佛拉体的年轻小鼠形成拉佛拉体。在已经出现拉佛拉体的老年小鼠中,Gys1-ASO 抑制了进一步的积累,明显阻止了晚期疾病中特征性的大拉佛拉体。拉佛拉体形成的抑制与星形胶质细胞增生的预防以及疾病免疫和神经炎症标志物失调表达的纠正趋势相关。拉佛拉病在以前健康的青少年中逐渐出现。我们的工作提供了原理证明,即针对 GYS1mRNA 的反义寡核苷酸可以预防和阻止这种灾难性癫痫的进展。