Suppr超能文献

硬脂酸通过自噬-CTSB-NLRP3 途径诱导肝细胞细胞焦亡。

Elaidic acid induced hepatocyte pyroptosis via autophagy-CTSB-NLRP3 pathway.

机构信息

College of Food Science and Engineering, Jilin University, Changchun, Jilin, 130062, People's Republic of China.

College of Food Science and Engineering, Jilin University, Changchun, Jilin, 130062, People's Republic of China; Key Laboratory of Zoonosis, Ministry of Education College of Veterinary Medicine, Jilin University, Changchun, Jilin, 130062, People's Republic of China.

出版信息

Food Chem Toxicol. 2023 Nov;181:114060. doi: 10.1016/j.fct.2023.114060. Epub 2023 Sep 23.

Abstract

Elaidic acid (EA, C18:1 trans) is a kind of principal Trans fatty acid (TFA) and is widely found in processed food. Pyroptosis is a form of programmed cell death, distinct from apoptosis and traditional necrosis. Excessive pyroptosis could induce body injury and serious inflammation. However, the effect of EA on pyroptosis has not been reported. In the study, we found that EA exposure caused liver damage and hepatocyte pyroptosis by testing GSDMD-N, Caspase 1, IL-18, and IL-1β in mice and HepG2 cells. Further exploring the mechanisms, we found that EA-induced pyroptosis depended on Cathepsin B (CTSB)-mediated NLRP3 inflammasome activation. Cell autophagy was closely related to lysosomes. Our study revealed that EA promoted hepatocyte autophagy, and activated autophagy induced lysosomal membrane permeabilization (LMP) and CTSB leakage. Inhibition of autophagy by 3-MA mitigated the CTSB leak, reduced the activation of the NLRP3 inflammasome, and then attenuated the EA-induced pyroptosis. In summary, these results indicated that EA induced hepatocyte pyroptosis via autophagy-CTSB-NLRP3 inflammasome pathway. The study revealed new insights into the toxicity mechanism of EA.

摘要

反式油酸(EA,C18:1 反式)是主要的反式脂肪酸(TFA)之一,广泛存在于加工食品中。细胞焦亡是一种程序性细胞死亡形式,与细胞凋亡和传统坏死不同。过度的细胞焦亡会导致机体损伤和严重的炎症。然而,EA 对细胞焦亡的影响尚未见报道。在这项研究中,我们通过检测小鼠和 HepG2 细胞中的 GSDMD-N、Caspase 1、IL-18 和 IL-1β,发现 EA 暴露会导致肝脏损伤和肝实质细胞焦亡。进一步探索其机制,我们发现 EA 诱导的细胞焦亡依赖于组织蛋白酶 B(CTSB)介导的 NLRP3 炎性体激活。细胞自噬与溶酶体密切相关。我们的研究表明,EA 促进了肝实质细胞自噬,激活的自噬诱导了溶酶体膜通透性(LMP)和 CTSB 渗漏。3-MA 抑制自噬减轻了 CTSB 的渗漏,减少了 NLRP3 炎性体的激活,从而减轻了 EA 诱导的细胞焦亡。综上所述,这些结果表明,EA 通过自噬-CTSB-NLRP3 炎性体途径诱导肝实质细胞焦亡。该研究揭示了 EA 毒性作用机制的新见解。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验