| 注册
首页|期刊导航|生物资源|Ⅰ型干扰素受体1基因敲除SD大鼠的遗传表型鉴定

Ⅰ型干扰素受体1基因敲除SD大鼠的遗传表型鉴定

蔡曾 鲜巧阳 包容 张璟怡 苏珊 龙子文 张璋 汤宏斌

生物资源2025,Vol.47Issue(6):551-555,5.
生物资源2025,Vol.47Issue(6):551-555,5.DOI:10.14188/j.ajsh.20251112002

Ⅰ型干扰素受体1基因敲除SD大鼠的遗传表型鉴定

Genetic phenotype identification of type Ⅰ interferon receptor 1-gene knockout SD rats

蔡曾 1鲜巧阳 1包容 1张璟怡 1苏珊 1龙子文 1张璋 1汤宏斌1

作者信息

  • 1. 武汉大学 动物实验中心/ABSL-Ⅲ实验室,湖北 武汉 430072
  • 折叠

摘要

Abstract

Type Ⅰ interferon(IFN-I)is a central cytokine in host antiviral immunity,and its signaling pathway is al-so closely associated with the pathogenesis of autoimmune diseases and tumors.Gene knockout animal models are crucial tools for studying the function of this pathway.However,the widely used type Ⅰ interferon receptor 1(IFNAR1)knock-out mouse model has limitations,including species differences and technical constraints,which restrict its translational value.To address this,we successfully generated an Ifnar1 knockout model in Sprague Dawley(SD)rats using CRIS-PR/Cas9 technology.Through genotyping of the offspring,we established a stable strain of Ifnar1-/-homozygous rats.Phenotypic analysis revealed no significant differences in morphology,behavior,or reproductive capability between the knockout and wild-type rats.Furthermore,immunohistochemical staining confirmed the complete absence of IFNAR1 protein expression in multiple tissues of Ifnar1-/-rats,including the liver,spleen,kidney,brain,and reproductive organs.The generation of this Ifnar1 knockout rat model provides a novel and promising preclinical platform for investigating the in vivo functions of the type Ⅰ interferon signaling pathway in a physiological context that more closely recapitulates human biology,and for evaluating the efficacy of related therapeutics.

关键词

Ⅰ型干扰素/基因敲除/大鼠模型

Key words

type Ⅰ interferon/gene knockout/rat model

分类

医药卫生

引用本文复制引用

蔡曾,鲜巧阳,包容,张璟怡,苏珊,龙子文,张璋,汤宏斌..Ⅰ型干扰素受体1基因敲除SD大鼠的遗传表型鉴定[J].生物资源,2025,47(6):551-555,5.

基金项目

国家重点研发计划(2021YFF0702002),湖北省实验动物研究科技项目(2022DFE022),湖北省自然科学基金(2024AFB103) (2021YFF0702002)

生物资源

1006-8376

访问量1
|
下载量0
段落导航相关论文