Jin Huan, Yin Shutao, Song Xinhua, Zhang Enxiang, Fan Lihong, Hu Hongbo
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Department of Nutrition and Health, College of Food Science and Nutritional Engineering, China Agricultural University, No17 Qinghua East Road, Haidian District, Beijing 100083, China.
College of Veterinary Medicine, China Agricultural University, No2 Yunamingyuan West Road, Haidian District, Beijing 100193, China.
Sci Rep. 2016 Apr 13;6:24455. doi: 10.1038/srep24455.
Patulin is a major mycotoxin found in fungal contaminated fruits and their derivative products. Previous studies showed that patulin was able to induce increase of reactive oxygen species (ROS) generation and oxidative stress was suggested to play a pivotal role in patulin-induced multiple toxic signaling. The objective of the present study was to investigate the functional role of p53 in patulin-induced oxidative stress. Our study demonstrated that higher levels of ROS generation and DNA damage were induced in wild-type p53 cell lines than that found in either knockdown or knockout p53 cell lines in response to patulin exposure, suggesting p53 activation contributed to patulin-induced ROS generation. Mechanistically, we revealed that the pro-oxidant role of p53 in response to patulin was attributed to its ability to suppress catalase activity through up-regulation of PIG3. Moreover, these in vitro findings were further validated in the p53 wild-type/knockout mouse model. To the best of our knowledge, this is the first report addressing the functional role of p53 in patulin-induced oxidative stress. The findings of the present study provided novel insights into understanding mechanisms behind oxidative stress in response to patulin exposure.
展青霉素是一种主要存在于受真菌污染的水果及其衍生产品中的霉菌毒素。先前的研究表明,展青霉素能够诱导活性氧(ROS)生成增加,并且氧化应激被认为在展青霉素诱导的多种毒性信号传导中起关键作用。本研究的目的是探讨p53在展青霉素诱导的氧化应激中的功能作用。我们的研究表明,在野生型p53细胞系中,与展青霉素暴露后的p53敲低或敲除细胞系相比,ROS生成水平和DNA损伤更高,这表明p53激活促进了展青霉素诱导的ROS生成。从机制上讲,我们发现p53在响应展青霉素时的促氧化作用归因于其通过上调PIG3来抑制过氧化氢酶活性的能力。此外,这些体外研究结果在p53野生型/敲除小鼠模型中得到了进一步验证。据我们所知,这是第一份关于p53在展青霉素诱导的氧化应激中的功能作用的报告。本研究结果为理解展青霉素暴露后氧化应激背后的机制提供了新的见解。