实用医学杂志 ›› 2023, Vol. 39 ›› Issue (3): 278-284.doi: 10.3969/j.issn.1006⁃5725.2023.03.003

• 基础研究 • 上一篇    下一篇

ANGPTL8敲除减轻DEN诱导的小鼠急性肝损伤

高玉玖1,2,3 胡蓉1,4 方晨1,3 李盼盼1,5 孟享1,5 郭兴荣1,3 冯莹1,3   

  1. 1 湖北医药学院附属太和医院,基础医学院,胚胎干细胞研究湖北省重点实验室(湖北十堰 442000); 2 湖北省十堰市太和医院肾内科(湖北十堰 442000);3 十堰市太和医院脐带血造血干细胞治疗临床医学 研究中心(湖北十堰 442000);4 湖北医药学院生物医学工程学院(湖北十堰 442000); 5 湖北医药学院第一临床学院(湖北十堰 442000)

  • 出版日期:2023-02-10 发布日期:2023-02-10
  • 通讯作者: 冯莹 E⁃mail:fyhappy.hello@163.com
  • 基金资助:
    国家自然科学基金项目(编号:82073232,82101632,81700769,81641028);十堰市科技局指导项目(编号:21Y38);湖北
    医药学院大学生创新项目(编号:202210929002)

ANGPTL8 knockout alleviates DEN⁃induced acute liver injury

GAO Yujiu*,HU Rong,FANG Chen, LI Panpan,MENG Xiang,GUO Xingrong,FENG Ying.   

  1. Hubei Key Laboratory of Embryonic Stem Cell Research School of Basic Medical SciencesTaihe HospitalHubei University of MedicineShiyan 442000China;*Depart⁃ ment of NephrologyTaihe HospitalShiyan 442000China;*Hubei Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem CellsTaihe HospitalShiyan 442000China
  • Online:2023-02-10 Published:2023-02-10
  • Contact: FENG Ying E⁃mail:fyhappy.hello@163.com

摘要:

目的 探讨血管生成素样蛋白 8(ANGPTL8)在 N⁃二乙基亚硝胺(DEN)诱导小鼠急性肝损伤 中的作用及机制。方法 选取雄性野生型(WT)和 ANGPTL8 敲除(ANGPTL8 KO)C57BL/6J 小鼠,腹腔注射 DEN(50 mg/kg)诱导急性肝损伤模型(15日龄各组32只,8周龄各组14只)。利用PCR和免疫荧光检测肝组 织和肝原代细胞中ANGPTL8的表达变化;试剂盒检测血清中ALT、AST含量;HE染色观察肝脏组织病理学 变化;流式细胞术和共聚焦显微镜分析肝原代细胞活性氧(ROS)累积差异;ELISA 检测血液中炎症因子 IL⁃6、IL⁃1β 含量;TUNEL 染色检测肝细胞凋亡水平。结果 DEN 诱导 3 d 显著上调肝脏中 ANGPTL8 表达; WT 小鼠相比,ANGPTL8 KO 可显著下调 DEN 诱导小鼠血清中 ALT AST、IL⁃6 IL⁃1β 水平;ANGPTL8 KO小鼠肝小叶紊乱程度、炎症细胞浸润、肝细胞淤血、空泡样变和坏死程度较轻;ANGPTL8 KO小鼠显著改 DEN诱导的肝细胞ROS累积和凋亡。结论 DEN上调肝脏中ANGPTL8表达,ANGPTL8进一步促进肝脏 急性炎症期ROS累积、炎症因子表达和肝细胞凋亡,从而加剧DEN诱导的急性肝损伤。

关键词:

ANGPTL8, 急性肝损伤, 活性氧, 炎症因子, 凋亡

Abstract:

Objective To investigate the role and mechanism of angiopoietin⁃like protein 8(ANGPTL8 in N⁃diethylnitrosamine(DEN)⁃induced acute liver injury in mice. Methods Male wild⁃type(WT)and ANGPTL8 knockout(ANGPTL8 KO)C57BL/6J mice were selected and injected with DEN(50 mg/kg)intraperitoneally to induce acute liver injury models(32 mice in each group at 15 days of age and 14 mice in each group at 8 weeks of age). The expression of ANGPTL8 in liver tissue and primary liver cells were detected by PCR and immunofluores⁃ cence;the levels of ALT and AST in serum were detected by the kit;the histopathological changes of liver were observed by HE staining;in the accumulation of reactive oxygen species(ROS)in primary liver cells was examined by flow cytometry and confocal microscopy;the levels of inflammatory factors IL⁃6 and IL⁃1β serum were detected by ELISA;the apoptosis of hepatocytes were detected by TUNEL staining. Results The expression of ANGPTL8 in the liver was significantly up⁃regulated at 3 days after DEN stimulation. Compared with WT mice,ANGPTL8 KO could significantly down⁃regulate the levels of ALT,AST,IL⁃6 and IL⁃1β in the serum induced by DEN;the hepatic lobular disorder,inflammation⁃related cell infiltration,hepatocyte congestion,vacuolar degeneration and necrosis induced by DEN were significantly improved in ANGPTL8 KO mice;the ROS accumulation and hepatocytes apoptosis induced by DEN were dramatically induced in ANGPTL8 KO mice. Conclusion DEN up⁃regulates the expression of ANGPTL8 in the liver,and ANGPTL8 further promotes the accumulation of ROS,the expression and secretion of inflammatory factors and hepatocyte apoptosis,which eventually aggravates DEN⁃induced acute liver injury.

Key words:

ANGPTL8, acute liver injury, reactive oxygen species, inflammatory factors, apoptosis