Reyes Juan F, Stone Karen, Ramos Jeanie, Maselli Andrew
Chicago State University, Department of Biological Sciences, 9501 S. King Drive, Chicago, IL 60628, USA.
Eukaryot Cell. 2009 Jun;8(6):852-7. doi: 10.1128/EC.00379-08. Epub 2009 Apr 10.
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.
Hirano小体是主要由肌动蛋白和肌动蛋白相关蛋白组成的细胞质内含物。据报道,在包括阿尔茨海默病和肌萎缩侧索硬化症在内的各种神经退行性疾病中会形成Hirano小体。尽管导致大脑中这些内含物形成的潜在分子机制尚不清楚,但盘基网柄菌内源性34 kDa肌动蛋白结合蛋白的C末端片段(CT)(氨基酸124至295)的表达会导致体内肌动蛋白内含物的形成。在本研究中,我们报告了一种诱导表达系统的开发,该系统使用诱导启动子系统(rnrB)来研究Hirano小体形成的早期阶段。通过将CT与绿色荧光蛋白(CT-GFP)融合,我们通过荧光显微镜、流式细胞术和蛋白质印迹分析监测了蛋白质的表达和定位。我们观察到诱导CT-GFP载体系统后形成的内含物数量和大小增加。延时显微镜研究表明,CT-GFP病灶与细胞皮层相关并融合形成单个大聚集体。透射电子显微镜进一步证明,这些内含物具有高度有序的超微结构,这是在各种神经退行性疾病患者的死后脑样本中观察到的Hirano小体的病理特征。总的来说,该系统提供了一种方法,可在真核模型中可视化和表征围绕早期肌动蛋白内含物形成的事件。