首都医科大学学报 ›› 2021, Vol. 42 ›› Issue (4): 568-574.doi: 10.3969/j.issn.1006-7795.2021.04.010

• 基础研究 • 上一篇    下一篇

肝细胞条件性Eva1a/Tmem166基因敲除小鼠的表型分析

陈建宏1, 林欣2, 冯金秋2, 丁鹏鹏1, 王苗苗1, 林琳1, 刘红1*, 吴静3*   

  1. 1.首都医科大学附属北京世纪坛医院消化内科,北京 100038;
    2.北京大学人类疾病基因研究中心,北京 100083;
    3.首都医科大学附属北京友谊医院消化内科 国家消化系统疾病临床医学研究中心 北京市消化疾病中心 消化疾病癌前病变北京市重点实验室,北京 100050
  • 收稿日期:2020-12-01 出版日期:2021-08-21 发布日期:2021-07-29
  • 基金资助:
    国家自然科学基金(81900505),北京市医院管理中心“青苗”计划资助项目(QML20200702),北京世纪坛医院青年基金(2018-q09)。

Phenotypic analysis of hepatocyte-specific Eva1a/Tmem166 gene knockout mice

Chen Jianhong1, Lin Xin2, Feng Jinqiu2, Ding Pengpeng1, Wang Miaomiao1, Lin Lin1, Liu Hong1*, Wu Jing3*   

  1. 1. Department of Gastroenterology, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China;
    2. Peking University Center for Human Diseases Genomics, Beijing 100083, China;
    3. Department of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, National Clinical Research Center for Digestive Diseases, Beijing Digestive Disease Center, Beijing Key Laboratory for Precancerous Lesion of Digestive Diseases, Beijing 100050, China
  • Received:2020-12-01 Online:2021-08-21 Published:2021-07-29
  • Contact: * E-mail:wujing36youyi@ccmu.edu.cn; liuhong_sjt@ccmu.edu.cn
  • Supported by:
    National Natural Science Foundation of China (81900505), Beijing Municipal Administration of Hospitals' Youth Programe (QML20200702), Youth Fund of Beijing Shijitan Hospital (2018-q09).

摘要: 目的 应用Cre-LoxP技术构建自噬相关基因Eva1a肝细胞条件性敲除小鼠初步探讨Eva1a基因敲除对小鼠表型的影响。方法 LoxP标记的Eva1aflox/+小鼠与Alb-Cre工具鼠通过多次繁殖杂交,构建纯合型肝细胞条件性Eva1a基因敲除(Eva1aflox/flox: Alb-Cre)小鼠模型。选取Eva1aflox/flox: Alb-Cre小鼠与同窝野生(Eva1aflox/flox)小鼠雌雄进行体质量、肝指数、肝脏组织学、肝功能、糖脂代谢以及细胞自噬等表型分析。结果 Eva1a纯合型基因敲除小鼠无胚胎致死现象,出生后一般生理状况良好。常规饲养条件下,肝脏Eva1a基因条件性敲除在小鼠体质量、肝脏外观以及组织结构、肝指数、肝功能、糖脂代谢及自噬等与野生型小鼠差异无统计学意义。结论 肝细胞条件性Eva1a基因敲除对小鼠生理条件下的表型无显著影响,为进一步探讨Eva1a在肝脏疾病状态下的作用及分子机制提供了动物模型。

关键词: Eva1a/Tmem166, 基因敲除, 肝脏, 表型

Abstract: Objective To construct mice models with hepatocyte-specific knockout of autophagy related gene Eva1a using Cre-LoxP technique, and to preliminarily explore the effect of Eva1a gene knockout on the phenotype of mice. Methods LoxP-labeled Eva1aflox/+ mice and Alb-Cre mice were used to construct homozygous mice models with hepatocyte-specific Eva1a gene knockout (Eva1aflox/flox: Alb-Cre) through multiple generations of hybridization. Eva1aflox/flox: Alb-Cre mice and Eva1aflox/flox mice were selected for phenotypic analysis, including body mass, liver index, liver histology, liver function, glycolipid metabolism, and autophagy level. Results There was no fetal death in homozygous Eva1a knockout mice, and no significant changes in the physiological condition were found. In conventional feeding conditions, hepatocyte-specific Eva1a knockout had no significant difference in body weight, liver appearance, tissue structure, liver index, liver function, glucose and lipid metabolism, and autophagy level from wild-type mice. Conclusion Hepatocyte-specific Eva1a gene knockout had no significant effect on the phenotype of mice in the physiological condition, and our study provided an animal model to further explore the role and molecular mechanism of Eva1a in liver disease.

Key words: Eva1a/Tmem166, gene knockout, liver, phenotype

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