Suppr超能文献

活体成像在髓鞘碱性蛋白启动子驱动荧光素酶转基因小鼠模型中的髓鞘化事件研究。

In Vivo Optical Imaging of Myelination Events in a Myelin Basic Protein Promoter-Driven Luciferase Transgenic Mouse Model.

机构信息

1 Translational In Vivo Model, Global Research Platform, Sanofi R&D, Framingham, MA, USA.

2 Multiple Sclerosis Cluster, Neuroscience Research, Sanofi R&D, Framingham, MA, USA.

出版信息

ASN Neuro. 2018 Jan-Dec;10:1759091418777329. doi: 10.1177/1759091418777329.

Abstract

The compact myelin sheath is important for axonal function, and its loss can lead to neuronal cell death and irreversible functional deficits. Myelin is vulnerable to a variety of metabolic, toxic, and autoimmune insults. In diseases like multiple sclerosis, there is currently no therapy to stop myelin loss, underscoring the need for neuroprotective and remyelinating therapies. Noninvasive, robust techniques are also needed to confirm the effect of such therapies in animal models. This article describes the generation, characterization, and potential uses for a myelin basic protein-luciferase (MBP-luci) transgenic mouse model, in which the firefly luciferase reporter gene is selectively controlled by the MBP promoter. In vivo bioluminescence imaging can be used to visualize and quantify demyelination and remyelination at the transcriptional level, noninvasively, and in real time. Transgenic mice were assessed in the cuprizone-induced model of demyelination, and luciferase activity highly correlated with demyelination and remyelination events as confirmed by both magnetic resonance imaging and postmortem histological analysis. Furthermore, MBP-luci mice demonstrated enhanced luciferase signal and remyelination in the cuprizone model after treatment with a peroxisome proliferator activated receptor-delta selective agonist and quetiapine. Imaging sensitivity was further enhanced by using CycLuc 1, a luciferase substrate, which has greater blood-brain barrier penetration. We demonstrated the utility of MBP-luci model in tracking myelin changes in real time and supporting target and therapeutic validation efforts.

摘要

紧凑的髓鞘对于轴突功能很重要,其丢失会导致神经元细胞死亡和不可逆转的功能缺陷。髓鞘容易受到各种代谢、毒性和自身免疫的影响。在多发性硬化症等疾病中,目前没有治疗方法可以阻止髓鞘丢失,这突显了神经保护和髓鞘再生治疗的必要性。还需要非侵入性、强大的技术来确认此类治疗方法在动物模型中的效果。本文介绍了髓鞘碱性蛋白-荧光素酶(MBP-luci)转基因小鼠模型的产生、特征和潜在用途,该模型中的荧光素酶报告基因受 MBP 启动子的选择性控制。体内生物发光成像可用于在转录水平上可视化和定量评估脱髓鞘和髓鞘再生,具有非侵入性和实时性。在脱髓鞘的铜诱导模型中评估了转基因小鼠,并且荧光素酶活性与磁共振成像和死后组织学分析证实的脱髓鞘和髓鞘再生事件高度相关。此外,在使用过氧化物酶体增殖物激活受体-δ选择性激动剂和喹硫平治疗后,MBP-luci 小鼠在铜诱导模型中表现出增强的荧光素酶信号和髓鞘再生。使用 CycLuc 1(一种具有更大血脑屏障穿透性的荧光素酶底物)进一步增强了成像灵敏度。我们证明了 MBP-luci 模型在实时跟踪髓鞘变化和支持靶标和治疗验证方面的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37fc/5987236/d46cba87eb9c/10.1177_1759091418777329-fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验