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In vivo longitudinal visualization of the brain neuroinflammatory response at the cellular level in LysM-GFP mice induced by 3-nitropropionic acid

机译:在3-硝基乙酸诱导的Lysm-GFP小鼠中的细胞水平下脑神经炎响应的体内纵向可视化

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摘要

Blood-brain barrier (BBB) dysfunction is related to the development of neuroinflammation in the central nervous system (CNS). Neuroinflammation has been implicated as one of the key factors in the pathogenesis of neurodegenerative diseases such as Alzheimer’s disease, Huntington’s disease, and Parkinson’s disease. Despite its importance, the impacts and underlying cellular mechanisms of chronic BBB impairment in neurodegenerative diseases are poorly understood. In this work, we performed a longitudinal intravital brain imaging of mouse model with neuroinflammation induced by 3-nitropropionic acid (3-NP). For this, we obtained a transgenic LysM-GFP mouse expressing the green fluorescence protein (GFP) in a subset of leukocytes. By using intravenously injected fluorescence blood tracers, we longitudinally observed dynamic cellular behaviors and the BBB integrity through a 30-day neuroinflammatory state. Vascular leakages in the cerebral cortex reflecting BBB impairment were observed at two weeks, which persisted to the third week, followed by a severe inflammatory response with massive leukocytes infiltration at day 30. These descriptions can help in the development of novel approaches to treat neurodegenerative conditions.
机译:血脑屏障(BBB)功能障碍与中枢神经系统(CNS)中神经炎症的发育有关。神经引起炎症被归因于神经变性疾病的发病机制,如阿尔茨海默病,亨廷顿疾病和帕金森病的关键因素之一。尽管重要的是,神经变性疾病慢性BBB损伤的影响和潜在的细胞机制尚不清楚。在这项工作中,我们对由3-硝基乙酸(3-NP)诱导的神经炎炎症进行小鼠模型进行了纵向脊髓瘤成像。为此,我们在白细胞的子集中获得了表达绿色荧光蛋白(GFP)的转基因Lysm-GFP小鼠。通过使用静脉内注射的荧光血液示踪剂,通过30天的神经炎症状态,我们纵向观察到动态细胞行为和BBB完整性。在两周内观察到反映BBB损伤的脑皮层中的血管泄漏,其持续到第三周,其次是在第30天具有巨大的白细胞浸润的严重炎症反应。这些描述可以帮助开发新的治疗神经变性病症的方法。

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