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首页> 外文期刊>Acta Neuropathologica Communications >Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography
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Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography

机译:光谱域光学相干断层扫描技术在非侵入性评估小儿和幼年神经元类固醇脂褐变小鼠模型中的视网膜改变

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IntroductionThe neuronal ceroid lipofuscinoses constitute a group of fatal inherited lysosomal storage diseases that manifest in profound neurodegeneration in the CNS. Visual impairment usually is an early symptom and selective degeneration of retinal neurons has been described in patients suffering from distinct disease subtypes. We have previously demonstrated that palmitoyl protein thioesterase 1 deficient ( Ppt1 -/- ) mice, a model of the infantile disease subtype, exhibit progressive axonal degeneration in the optic nerve and loss of retinal ganglion cells, faithfully reflecting disease severity in the CNS. Here we performed spectral domain optical coherence tomography (OCT) in Ppt1 -/- and ceroid lipofuscinosis neuronal 3 deficient ( Cln3 -/- ) mice, which are models of infantile and juvenile neuronal ceroid lipofuscinosis, respectively, in order to establish a non-invasive method to assess retinal alterations and monitor disease severity in vivo . ResultsBlue laser autofluorescence imaging revealed increased accumulation of autofluorescent storage material in the inner retinae of 7-month-old Ppt1 -/- and of 16-month-old Cln3 -/- mice in comparison with age-matched control littermates. Additionally, optical coherence tomography demonstrated reduced thickness of retinae in knockout mice in comparison with age-matched control littermates. High resolution scans and manual measurements allowed for separation of different retinal composite layers and revealed a thinning of layers in the inner retinae of both mouse models at distinct ages. OCT measurements correlated well with subsequent histological analysis of the same retinae. ConclusionsThese results demonstrate the feasibility of OCT to assess neurodegenerative disease severity in mouse models of neuronal ceroid lipofuscinosis and might have important implications for diagnostic evaluation of disease progression and therapeutic efficacy in patients. Moreover, the non-invasive method allows for longitudinal studies in experimental models, reducing the number of animals used for research.
机译:简介神经元类固醇脂褐藻糖脂构成一组致命的遗传性溶酶体贮积病,表现为中枢神经系统严重的神经变性。视力障碍通常是一种早期症状,在患有不同疾病亚型的患者中已经描述了视网膜神经元的选择性变性。先前我们已经证明,棕榈酰蛋白硫酯酶1缺陷型(Ppt1 -/-)小鼠是婴儿疾病亚型的模型,在视神经中表现出进行性轴突变性和视网膜神经节细胞丢失,如实反映中枢神经系统疾病的严重程度。在这里,我们对Ppt1 -/-和类固醇脂褐藻病神经元3缺陷(Cln3 -/-)小鼠进行了光谱域光学相干断层扫描(OCT),这是婴儿和小儿模型。为了建立一种非侵入性的方法来评估视网膜病变并在体内监测疾病的严重程度,分别对青少年神经元性类脂褐藻病进行了研究。结果蓝色激光自发荧光成像显示7个月大的Ppt1 -/-和16个月大的Cln3 -/-的视网膜内部自发荧光存储材料的积累增加与年龄匹配的对照同窝仔相比。此外,与年龄匹配的对照同窝仔相比,光学相干断层扫描显示出基因敲除小鼠的视网膜厚度减少。高分辨率扫描和手动测量允许分离不同的视网膜复合层,并揭示了两个小鼠模型在不同年龄时视网膜内侧的层变薄。 OCT测量值与随后对同一视网膜的组织学分析密切相关。结论这些结果表明,OCT可以评估神经元类脂褐藻病小鼠模型中神经退行性疾病的严重程度,并且可能对患者疾病进展和治疗效果的诊断评估具有重要意义。此外,非侵入性方法允许在实验模型中进行纵向研究,从而减少了用于研究的动物数量。

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