首页|斑马鱼TDP43负调控工型干扰素的表达

斑马鱼TDP43负调控工型干扰素的表达

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TDP43是一种DNA/RNA结合蛋白,属于异质核糖核蛋白家族成员,在调控转录、mRNA稳定性及翻译等方面发挥重要作用.近年来有报道表明哺乳类TDP43参与了炎症和免疫反应,然而TDP43在免疫应答中的功能机制还不清楚.探索了斑马鱼TDP43在先天免疫反应中的功能.首先通过同源比对及构建TDP43的系统进化树,分析了 TDP43在不同物种中的进化特征,结果表明TDP43在哺乳类和鱼类中的相似度很高(60%以上).SVCV病毒感染斑马鱼和CIK细胞后,检测TDP43在各组织和细胞中表达发现,(脑、眼睛、肠、鳃、皮肤、心脏、肝脏和肾脏)和CIK细胞中均上调.体外构建TDP43真核表达载体或合成TDP43的小干扰RNA,在CIK细胞中过表达TDP43能够抑制了 Ⅰ型干扰素表达,而敲降TDP43则上调了 Ⅰ型干扰素的表达.此外,亚细胞定位分析表明TDP43主要定位于细胞核,说明TDP43可能是在细胞核中调控基因的转录而控制先天免疫反应.总之,我们研究了斑马鱼TDP43在响应病毒感染及在先天免疫反应中的功能.
Danio rerio TDP43 negatively regulates the expression of type Ⅰ IFN
TDP43,a DNA/RNA binding protein belonging to the heterologous ribonucleoprotein family,plays an important role in the regulation of transcription,mRNA stability,and translation.Recent studies showed the involvement of mammalian TDP43 in inflammation and immune response,yet the mechanism governing TDP43's function in immune response remained unclear.This study delved into the role of zebrafish TDP43 in innate immune response.Firstly,amino acid alignment and phylo-genetic tree showed that TDP43 has a high similarity(over 60%)in mammals and fish.Upon infection with SVCV,the expres-sion of TDP43 in zebrafish and CIK cells exhibited an upregulation in various organs,including the brain,eyes,intestine,gills,skin,heart,liver,and kidney,as well as CIK cells.Overexpression of TDP43 in CIK cells can inhibit the expression of type Ⅰ in-terferon,while knockdown of TDP43 led to an upregulation of type Ⅰ interferon.In addition,subcellular localization analysis showed that TDP43 was mainly located in the nucleus,indicating that TDP43 might control innate immune response by regula-ting gene transcription in the nucleus.In summary,this study offered insights into the role of zebrafish TDP43 in responding to viral infections.

zebrafishTDP43interferongrass carp kidney cellsexpressionregulation

胡美玲、于婷婷、卢君焱、花佳利、龚慧莹、杨珊珊、胡成钰、徐小文

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南昌大学生命科学学院,江西南昌 330031

斑马鱼 TDP43 干扰素 草鱼肾细胞 表达 调控

国家自然科学基金地区资助项目

32160872

2024

南昌大学学报(理科版)
南昌大学

南昌大学学报(理科版)

CSTPCD
影响因子:0.418
ISSN:1006-0464
年,卷(期):2024.48(2)
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