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Formation of Hirano Bodies after Inducible Expression of a Modified Form of an Actin-Cross-Linking Protein

机译:诱导表达的肌动蛋白交联蛋白的修饰形式后平野机构的形成。

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Hirano bodies are cytoplasmic inclusions composed mainly of actin and actin-associated proteins. The formation of Hirano bodies during various neurodegenerative disorders, including Alzheimer's disease and amyotrophic lateral sclerosis, has been reported. Although the underlying molecular mechanisms that lead to the formation of these inclusions in the brain are not known, expression of the C-terminal fragment (CT) (amino acids 124 to 295) from the endogenous 34-kDa actin-binding protein of Dictyostelium discoideum leads to the formation of actin inclusions in vivo. In the current study, we report the development of an inducible expression system to study the early phases of Hirano body formation using an inducible promoter system (rnrB). By fusing the CT to a green fluorescent protein (CT-GFP), we monitored protein expression and localization by fluorescence microscopy, flow cytometry, and Western blot analysis. We observed an increase in the number and size of inclusions formed following induction of the CT-GFP vector system. Time-lapse microscopy studies revealed that the CT-GFP foci associated with the cell cortex and fused to form a single large aggregate. Transmission electron microscopy further demonstrates that these inclusions have a highly ordered ultrastructure, a pathological hallmark of Hirano bodies observed in postmortem brain samples from patients with various neurodegenerative disorders. Collectively, this system provides a method to visualize and characterize the events that surround early actin inclusion formation in a eukaryotic model.
机译:平野小体是主要由肌动蛋白和肌动蛋白相关蛋白组成的胞质内含物。据报道,在各种神经退行性疾病,包括阿尔茨海默氏病和肌萎缩性侧索硬化症中,Hirano体的形成。尽管导致这些内含物在大脑中形成的潜在分子机制尚不清楚,但其内源性34-kDa肌动蛋白结合蛋白的C末端片段(CT)(氨基酸124至295)的表达> Dictyostelium discoideum 导致体内肌动蛋白内含物的形成。在当前的研究中,我们报告了一种诱导型表达系统的开发,以使用诱导型启动子系统( rnrB )研究平野身体形成的早期阶段。通过将CT融合到绿色荧光蛋白(CT-GFP),我们通过荧光显微镜,流式细胞术和Western印迹分析监测了蛋白的表达和定位。我们观察到诱导CT-GFP载体系统后形成的内含物的数量和大小都有所增加。延时显微镜研究表明,CT-GFP灶与细胞皮层相关并融合形成单个大的聚集体。透射电子显微镜进一步证明这些包裹体具有高度有序的超微结构,这是在患有各种神经退行性疾病的患者的死后脑样本中观察到的平野尸体的病理学特征。总的来说,该系统提供了一种方法来可视化和表征真核模型中围绕早期肌动蛋白包涵体形成的事件。

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