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美洲大蠊肽Periplanetasin-4可抑制艰难梭菌毒素A诱导的小鼠肠道细胞毒性和炎症反应。

The American cockroach peptide periplanetasin-4 inhibits Clostridium difficile toxin A-induced cell toxicities and inflammatory responses in the mouse gut.

作者信息

Yoon I Na, Lu Li Fang, Hong Ji, Zhang Peng, Kim Dae Hong, Kang Jin Ku, Hwang Jae Sam, Kim Ho

机构信息

Division of Life Science and Chemistry, College of Natural Science, Daejin University, Pocheon, Gyeonggido, 11159, Korea.

Hainan Institute of Science and Technology, Haikou, 571126, China.

出版信息

J Pept Sci. 2017 Nov;23(11):833-839. doi: 10.1002/psc.3046. Epub 2017 Sep 26.

Abstract

Many reports have shown that crude extracts of the American cockroach have therapeutic effects on inflammation. In a previous study, our research group showed that an antimicrobial peptide (Periplanetasin-2) derived from the American cockroach via de novo transcriptome analysis inhibited apoptosis of human colonocytes and inflammatory responses of the mouse gut caused by Clostridium difficile toxin A. Here, we examined whether Periplanetasin-4 (Peri-4), another antimicrobial peptide identified via de novo transcriptome analysis of the American cockroach, could also inhibit the various toxicities induced by C. difficile toxin A. We found that Peri-4 significantly reduced the cell viability loss and cell apoptosis caused by toxin A in vitro. Peri-4 also ameliorated the severe inflammatory responses seen in the toxin A-induced mouse enteritis model, rescuing the villus disruption and interleukin-6 production induced by luminal injection of toxin A into the mouse gut. Mechanistically, we found that Peri-4 could reduce toxin A-induced reactive oxygen species production to inhibit the activations of p38MAPK and p21 , which are critical for the cell damages induced by toxin A. These results collectively suggest that the Peri-4 may be a potential therapeutic agent for treating toxin A-induced pseudomembranous colitis. Copyright © 2017 European Peptide Society and John Wiley & Sons, Ltd.

摘要

许多报告表明,美洲大蠊的粗提物具有抗炎治疗作用。在之前的一项研究中,我们的研究小组通过从头转录组分析发现,一种源自美洲大蠊的抗菌肽(Periplanetasin-2)可抑制人结肠细胞的凋亡以及艰难梭菌毒素A引起的小鼠肠道炎症反应。在此,我们研究了通过美洲大蠊从头转录组分析鉴定出的另一种抗菌肽Periplanetasin-4(Peri-4)是否也能抑制艰难梭菌毒素A诱导的各种毒性。我们发现,Peri-4在体外显著降低了毒素A引起的细胞活力丧失和细胞凋亡。Peri-4还改善了毒素A诱导的小鼠肠炎模型中出现的严重炎症反应,挽救了向小鼠肠道腔内注射毒素A所诱导的绒毛破坏和白细胞介素-6的产生。从机制上讲,我们发现Peri-4可以减少毒素A诱导的活性氧生成,从而抑制p38MAPK和p21的激活,而这两者对于毒素A诱导的细胞损伤至关重要。这些结果共同表明,Peri-4可能是治疗毒素A诱导的伪膜性结肠炎的潜在治疗剂。版权所有© 2017欧洲肽学会和约翰·威利父子有限公司。

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