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腺苷酸激酶 1 在日本血吸虫尾蚴表皮发育中的作用。

Role of adenylate kinase 1 in the integument development of Schistosoma japonicum schistosomula.

机构信息

Medical department, City College, Wuhan University of Science and Technology, Wuhan, 430083, China.

Department of Blood Transfusion, Henan Provincial People's Hospital, People's Hospital of Zhengzhou Universit,Zhengzhou 450003,China.

出版信息

Acta Trop. 2020 Jul;207:105467. doi: 10.1016/j.actatropica.2020.105467. Epub 2020 Apr 8.

Abstract

Schistosomula antigens play an important role in the growth and development of Schistosoma japonicum. We investigated the role of S. japonicum adenylate kinase 1 (SjAK1) in the growth and development of schistosomula. Quantitative real-time PCR showed that SjAK1 mRNA was expressed in all schistosomula stages, but increased gradually with the development of S. japonicum schistosomula. Using immunohistochemical techniques, the AK1 protein was found to be mainly distributed in the tegument and in some parenchymal tissues of the schistosomula. Double-stranded RNA-mediated knockdown of AK1 reduced AK1 mRNA transcripts by more than 90%; western blot analysis demonstrated that AK1 protein expression decreased by 66%. Scanning electron microscopy following RNA-mediated AK1 knockdown demonstrated that the sensory papillae degenerated significantly. Transmission electron microscopy demonstrated that the mean thickness of the tegument in the SjAK1 interference group was lower than that in the negative control group. Terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) suggested that, compared with the negative control group, apoptosis increased in the interference group. These results show that AK1 may be involved in the growth and development of S. japonicum schistosomula, and thus may be a target when developing treatments for schistosomiasis.

摘要

日本血吸虫的童虫抗原在其生长和发育中起着重要作用。我们研究了日本血吸虫腺嘌呤激酶 1(SjAK1)在童虫生长和发育中的作用。实时定量 PCR 显示 SjAK1mRNA 在所有童虫期都有表达,但随着日本血吸虫童虫的发育逐渐增加。用免疫组织化学技术发现 AK1 蛋白主要分布在童虫的表皮和一些实质组织中。双链 RNA 介导的 AK1 敲低使 AK1mRNA 转录物减少了 90%以上;Western blot 分析表明 AK1 蛋白表达减少了 66%。RNA 介导的 AK1 敲低后的扫描电镜显示感觉乳突明显退化。透射电镜显示 SjAK1 干扰组的表皮平均厚度低于阴性对照组。末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)表明,与阴性对照组相比,干扰组的细胞凋亡增加。这些结果表明 AK1 可能参与了日本血吸虫童虫的生长和发育,因此可能是开发血吸虫病治疗方法的一个靶点。

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