Moon Eun-Kyung, Hong Yeonchul, Chung Dong-Il, Kong Hyun-Hee
Department of Parasitology, Kyungpook National University School of Medicine, Taegu, Republic of Korea.
Mol Biochem Parasitol. 2012 Oct;185(2):121-6. doi: 10.1016/j.molbiopara.2012.07.008. Epub 2012 Aug 14.
Using the microarray to identify encystation mediating factors, significantly higher expression of a cysteine protease gene was observed in cysts, compared with trophozoites. Results of real-time PCR analysis also showed a magnificent increase of cysteine protease levels during encystation of Acanthamoeba. We named the gene cyst specific cysteine protease (cscp) of Acanthamoeba. The purified recombinant protein of CSCP showed activities of papain and cathepsin B against the substrates. During encystation, EGFP fused CSCP showed colocalization with LysoTracker, an autophagosome marker, in transiently transfected amoeba. Amoeba transfected with siRNA against cscp was unable to form mature cysts. Undigested mitochondria in vacuole like structures were observed in cscp siRNA treated cells by transmission electron microscopy. These results provide evidence of the important role of CSCP in autophagosomal degradation of cell constituents, particularly mitochondria, during encystation of Acanthamoeba.
利用微阵列鉴定包囊化介导因子,与滋养体相比,在包囊中观察到一种半胱氨酸蛋白酶基因的表达显著更高。实时PCR分析结果还显示,棘阿米巴包囊化过程中半胱氨酸蛋白酶水平大幅增加。我们将该基因命名为棘阿米巴的包囊特异性半胱氨酸蛋白酶(cscp)。纯化的CSCP重组蛋白对底物显示出木瓜蛋白酶和组织蛋白酶B的活性。在包囊化过程中,EGFP融合的CSCP在瞬时转染的变形虫中与自噬体标记物LysoTracker共定位。用针对cscp的siRNA转染的变形虫无法形成成熟的包囊。通过透射电子显微镜在cscp siRNA处理的细胞中观察到空泡样结构中未消化的线粒体。这些结果提供了证据,证明CSCP在棘阿米巴包囊化过程中对细胞成分尤其是线粒体的自噬体降解起重要作用。