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IRE1α 分支而非 PERK 分支的未折叠蛋白反应的激活有助于展青霉素 B1 诱导的肝毒性。

Activation of the IRE1α Arm, but not the PERK Arm, of the Unfolded Protein Response Contributes to Fumonisin B1-Induced Hepatotoxicity.

机构信息

Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Food Science and Nutritional Engineering, Beijing Key Laboratory for Food Non-thermal Processing, China Agricultural University, Beijing 100083, China.

College of Veterinary Medicine, China Agricultural University, No. 2 Yunamingyuan West Road, Haidian District, Beijing 100193, China.

出版信息

Toxins (Basel). 2020 Jan 16;12(1):55. doi: 10.3390/toxins12010055.

Abstract

Previous studies by us or others have shown that endoplasmic reticulum (ER) stress was activated by fumonisin 1 (FB1) exposure, which is considered to be a critical event in the FB1-induced toxic effect. However, the detailed mechanisms underlying FB1-induced ER stress-mediated liver toxicity remain elusive. The objectives of the present study were designed to address the following issues: (1) the contribution of each arm of the unfolded protein response (UPR); (2) the downstream targets of ER stress that mediated FB1-induced liver toxicity; and (3) the relationship between ER stress and oxidative stress triggered by FB1. We also investigated whether the inhibition of ER stress by its inhibitor could offer protection against FB1-induced hepatotoxicity in vivo, which has not been critically addressed previously. The results showed that the activation of the IRE1α axis, but not of the PERK axis, of UPR contributed to FB1-induced ER stress-mediated hepatocyte toxicity; the activation of the Bax/Bak-mediated mitochondrial pathway lay downstream of IRE1α to trigger mitochondrial-dependent apoptosis in response to FB1; FB1-induced oxidative stress and ER stress augmented each other through a positive feedback mechanism; tauroursodeoxycholic acid (TUDCA)-mediated ER stress inactivation is an effective approach to counteract FB1-induced hepatotoxicity in vivo. The data of the present study allow us to better understand the mechanisms of FB1-induced hepatotoxicity.

摘要

先前我们或其他人的研究表明,内质网(ER)应激被伏马菌素 1(FB1)暴露激活,这被认为是 FB1 诱导的毒性作用中的一个关键事件。然而,FB1 诱导的 ER 应激介导的肝毒性的详细机制仍不清楚。本研究的目的是解决以下问题:(1)未折叠蛋白反应(UPR)各分支的贡献;(2)介导 FB1 诱导的肝毒性的 ER 应激的下游靶标;以及(3)FB1 引发的 ER 应激与氧化应激之间的关系。我们还研究了 ER 应激抑制剂是否可以在体内抑制 FB1 诱导的肝毒性,这在以前的研究中尚未得到严格解决。结果表明,UPR 的 IRE1α 轴的激活,但不是 PERK 轴的激活,有助于 FB1 诱导的 ER 应激介导的肝细胞毒性;IRE1α 激活下游 Bax/Bak 介导的线粒体途径,以响应 FB1 触发线粒体依赖性细胞凋亡;FB1 诱导的氧化应激和 ER 应激通过正反馈机制相互增强;牛磺熊脱氧胆酸(TUDCA)介导的 ER 应激失活是一种有效的方法,可以在体内对抗 FB1 诱导的肝毒性。本研究的数据使我们能够更好地理解 FB1 诱导的肝毒性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e1e/7020448/1d6d4baab313/toxins-12-00055-g001.jpg

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