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Progressive Retinal Degeneration and Glial Activation in the CLN6nclf Mouse Model of Neuronal Ceroid Lipofuscinosis: A Beneficial Effect of DHA and Curcumin Supplementation

机译:CLN6nclf小鼠神经元性脂质脂肪增多症的CLN6nclf小鼠模型中的进行性视网膜变性和胶质细胞激活:DHA和姜黄素补充的有益作用。

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摘要

Neuronal ceroid lipofuscinosis (NCL) is a group of neurodegenerative lysosomal storage disorders characterized by vision loss, mental and motor deficits, and spontaneous seizures. Neuropathological analyses of autopsy material from NCL patients and animal models revealed brain atrophy closely associated with glial activity. Earlier reports also noticed loss of retinal cells and reactive gliosis in some forms of NCL. To study this phenomenon in detail, we analyzed the ocular phenotype of CLN6nclf mice, an established mouse model for variant-late infantile NCL. Retinal morphometry, immunohistochemistry, optokinetic tracking, electroretinography, and mRNA expression were used to characterize retinal morphology and function as well as the responses of Müller cells and microglia. Our histological data showed a severe and progressive degeneration in the CLN6nclf retina co-inciding with reactive Müller glia. Furthermore, a prominent phenotypic transformation of ramified microglia to phagocytic, bloated, and mislocalized microglial cells was identified in CLN6nclf retinas. These events overlapped with a rapid loss of visual perception and retinal function. Based on the strong microglia reactivity we hypothesized that dietary supplementation with immuno-regulatory compounds, curcumin and docosahexaenoic acid (DHA), could ameliorate microgliosis and reduce retinal degeneration. Our analyses showed that treatment of three-week-old CLN6nclf mice with either 5% DHA or 0.6% curcumin for 30 weeks resulted in a reduced number of amoeboid reactive microglia and partially improved retinal function. DHA-treatment also improved the morphology of CLN6nclf retinas with a preserved thickness of the photoreceptor layer in most regions of the retina. Our results suggest that microglial reactivity closely accompanies disease progression in the CLN6nclf retina and both processes can be attenuated with dietary supplemented immuno-modulating compounds.
机译:神经元类脂褐质沉着病(NCL)是一组神经退行性溶酶体贮积病,其特征在于视力丧失,精神和运动缺陷以及自发性癫痫发作。 NCL患者和动物模型的尸检材料的神经病理学分析显示,脑萎缩与神经胶质活动密切相关。较早的报道还注意到某些形式的NCL视网膜细胞丢失和反应性神经胶质增生。为了详细研究这种现象,我们分析了CLN6 nclf 小鼠的眼表型,CLN6 nclf 小鼠是晚期变异型NCL的已建立小鼠模型。视网膜形态测定,免疫组化,光动力学跟踪,视网膜电图和mRNA表达用于表征视网膜形态和功能以及Müller细胞和小胶质细胞的反应。我们的组织学数据显示,CLN6 nclf 视网膜与反应性Müller胶质细胞同时发生严重和进行性变性。此外,在CLN6 nclf 视网膜中发现了分枝的小胶质细胞向吞噬,肿和错误定位的小胶质细胞的显着表型转化。这些事件与视觉感知和视网膜功能的快速丧失重叠。基于强烈的小胶质细胞反应性,我们假设饮食中添加免疫调节化合物姜黄素和二十二碳六烯酸(DHA)可以减轻小胶质细胞增生并减少视网膜变性。我们的分析表明,用5%DHA或0.6%姜黄素治疗三周大的CLN6 nclf 小鼠30周可减少变形虫反应性小胶质细胞数量,并部分改善视网膜功能。 DHA处理还改善了CLN6 nclf 视网膜的形态,并在视网膜的大部分区域保留了感光层的厚度。我们的结果表明,小胶质细胞反应性与CLN6 nclf 视网膜中的疾病进展密切相关,并且饮食补充的免疫调节化合物可以减弱这两个过程。

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