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Charcot-Marie-Tooth 4C 型神经病模型中的基因替代疗法。

Gene replacement therapy in a model of Charcot-Marie-Tooth 4C neuropathy.

机构信息

Neuroscience Laboratory and Neurology Clinics, The Cyprus Institute of Neurology and Genetics and Cyprus School of Molecular Medicine, Nicosia, Cyprus.

Department of Neuroscience and Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

Brain. 2019 May 1;142(5):1227-1241. doi: 10.1093/brain/awz064.

Abstract

Charcot-Marie-Tooth disease type 4C is the most common recessively inherited demyelinating neuropathy that results from loss of function mutations in the SH3TC2 gene. Sh3tc2-/- mice represent a well characterized disease model developing early onset progressive peripheral neuropathy with hypo- and demyelination, slowing of nerve conduction velocities and disturbed nodal architecture. The aim of this project was to develop a gene replacement therapy for treating Charcot-Marie-Tooth disease type 4C to rescue the phenotype of the Sh3tc2-/- mouse model. We generated a lentiviral vector LV-Mpz.SH3TC2.myc to drive expression of the human SH3TC2 cDNA under the control of the Mpz promoter specifically in myelinating Schwann cells. The vector was delivered into 3-week-old Sh3tc2-/- mice by lumbar intrathecal injection and gene expression was assessed 4-8 weeks after injection. Immunofluorescence analysis showed presence of myc-tagged human SH3TC2 in sciatic nerves and lumbar roots in the perinuclear cytoplasm of a subset of Schwann cells, in a dotted pattern co-localizing with physiologically interacting protein Rab11. Quantitative PCR analysis confirmed SH3TC2 mRNA expression in different peripheral nervous system tissues. A treatment trial was initiated in 3 weeks old randomized Sh3tc2-/- littermate mice which received either the full or mock (LV-Mpz.Egfp) vector. Behavioural analysis 8 weeks after injection showed improved motor performance in rotarod and foot grip tests in treated Sh3tc2-/- mice compared to mock vector-treated animals. Moreover, motor nerve conduction velocities were increased in treated Sh3tc2-/- mice. On a structural level, morphological analysis revealed significant improvement in g-ratios, myelin thickness, and ratios of demyelinated fibres in lumbar roots and sciatic nerves of treated Sh3tc2-/- mice. Finally, treated mice also showed improved nodal molecular architecture and reduction of blood neurofilament light levels, a clinically relevant biomarker for axonal injury/degeneration. This study provides a proof of principle for viral gene replacement therapy targeted to Schwann cells to treat Charcot-Marie-Tooth disease type 4C and potentially other similar demyelinating inherited neuropathies.

摘要

遗传性运动感觉神经病 4C 型是最常见的隐性遗传性脱髓鞘神经病,由 SH3TC2 基因突变导致功能丧失引起。Sh3tc2-/- 小鼠是一种特征明确的疾病模型,表现为早期发病的进行性周围神经病,伴有Hypo-和脱髓鞘、神经传导速度减慢以及神经节结构紊乱。本项目的目的是开发一种针对遗传性运动感觉神经病 4C 型的基因替代疗法,以挽救 Sh3tc2-/- 小鼠模型的表型。我们生成了一种慢病毒载体 LV-Mpz.SH3TC2.myc,以在髓鞘形成施万细胞中受 Mpz 启动子控制,驱动人 SH3TC2 cDNA 的表达。该载体通过腰椎蛛网膜下腔注射递送至 3 周龄的 Sh3tc2-/- 小鼠中,并在注射后 4-8 周评估基因表达。免疫荧光分析显示,在 Sh3tc2-/- 小鼠的坐骨神经和腰神经根中,在施万细胞的核周细胞质中存在 Myc 标记的人 SH3TC2,呈点状,与生理相互作用的蛋白 Rab11 共定位。定量 PCR 分析证实了不同周围神经系统组织中 SH3TC2 mRNA 的表达。在 3 周龄随机 Sh3tc2-/- 同窝仔鼠中启动了治疗试验,这些仔鼠接受了完整的或模拟(LV-Mpz.Egfp)载体的治疗。注射 8 周后的行为分析显示,与模拟载体治疗的动物相比,治疗的 Sh3tc2-/- 小鼠在旋转棒和足部抓握测试中的运动表现得到改善。此外,治疗的 Sh3tc2-/- 小鼠的运动神经传导速度增加。在结构水平上,形态学分析显示,治疗的 Sh3tc2-/- 小鼠的腰椎神经根和坐骨神经中的 g-比、髓鞘厚度和脱髓鞘纤维比例均有显著改善。最后,治疗小鼠还显示出节点分子结构的改善和血液神经丝轻链水平的降低,这是轴突损伤/退化的一种临床相关生物标志物。本研究为针对施万细胞的病毒基因替代疗法治疗遗传性运动感觉神经病 4C 型和潜在的其他类似脱髓鞘遗传性神经病提供了原理验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d255/6487329/80fa6b836056/awz064f1.jpg

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