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脊髓小脑共济失调 7 型视网膜变性小鼠模型中的细胞死亡机制

Cell Death Mechanisms in a Mouse Model of Retinal Degeneration in Spinocerebellar Ataxia 7.

机构信息

Inserm U1138. Centre des Recherches des Cordeliers, 15, rue de l'Ecole de Médecine, 78006 Paris, France; Université Pierre et Marie Curie, France; Université Paris Descartes, France.

Inserm U1138. Centre des Recherches des Cordeliers, 15, rue de l'Ecole de Médecine, 78006 Paris, France; Université Pierre et Marie Curie, France; Université Paris Descartes, France.

出版信息

Neuroscience. 2019 Feb 21;400:72-84. doi: 10.1016/j.neuroscience.2018.12.051. Epub 2019 Jan 6.

DOI:10.1016/j.neuroscience.2018.12.051
PMID:30625334
Abstract

Spino-cerebellar ataxia type 7 (SCA7) is a polyglutamine (polyQ) disorder characterized by neurodegeneration of the brain, cerebellum, and retina caused by a polyglutamine expansion in ataxin7. The presence of an expanded polyQ tract in a mutant protein is known to induce protein aggregation, cellular stress, toxicity, and finally cell death. However, the consequences of the presence of mutant ataxin7 in the retina and the mechanisms underlying photoreceptor degeneration remain poorly understood. In this study, we show that in a retinal SCA7 mouse model, polyQ ataxin7 induces stress within the retina and activates Muller cells. Moreover, unfolded protein response and autophagy are activated in SCA7 photoreceptors. We have also shown that the photoreceptor death does not involve a caspase-dependent apoptosis but instead involves apoptosis inducing factor (AIF) and Leukocyte Elastase Inhibitor (LEI/L-DNase II). When these two cell death effectors are downregulated by their siRNA, a significant reduction in photoreceptor death is observed. These results highlight the consequences of polyQ protein expression in the retina and the role of caspase-independent pathways involved in photoreceptor cell death.

摘要

脊髓小脑共济失调 7 型(SCA7)是一种多聚谷氨酰胺(polyQ)疾病,其特征是脑、小脑和视网膜的神经退行性变,由 ataxin7 中的多聚谷氨酰胺扩展引起。已知突变蛋白中存在扩展的 polyQ 片段会诱导蛋白聚集、细胞应激、毒性,最终导致细胞死亡。然而,突变 ataxin7 在视网膜中的存在的后果以及光感受器变性的机制仍知之甚少。在这项研究中,我们表明在视网膜 SCA7 小鼠模型中,polyQ ataxin7 会在视网膜内引起应激并激活 Muller 细胞。此外,未折叠蛋白反应和自噬在 SCA7 光感受器中被激活。我们还表明,光感受器死亡不涉及 caspase 依赖性细胞凋亡,而是涉及凋亡诱导因子(AIF)和白细胞弹性蛋白酶抑制剂(LEI/L-DNase II)。当通过 siRNA 下调这两种细胞死亡效应物时,观察到光感受器死亡显著减少。这些结果强调了 polyQ 蛋白在视网膜中的表达的后果以及 caspase 非依赖性途径在光感受器细胞死亡中的作用。

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引用本文的文献

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Life (Basel). 2022 Dec 22;13(1):23. doi: 10.3390/life13010023.
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PolyQ length co-evolution in neural proteins.神经蛋白中多聚谷氨酰胺长度的共同进化
NAR Genom Bioinform. 2021 May 14;3(2):lqab032. doi: 10.1093/nargab/lqab032. eCollection 2021 Jun.
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Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review.多聚谷氨酰胺常染色体显性遗传性脊髓小脑共济失调的眼科表现与遗传学:综述
Front Neurosci. 2020 Aug 21;14:892. doi: 10.3389/fnins.2020.00892. eCollection 2020.
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Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.脊髓小脑性共济失调 7 型的分子靶点和治疗策略。
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Delineating the role of eIF2α in retinal degeneration.阐明 eIF2α 在视网膜变性中的作用。
Cell Death Dis. 2019 May 28;10(6):409. doi: 10.1038/s41419-019-1641-y.