Suppr超能文献

在体外和体内,miRNA - 133通过靶向IRAK - 1的TLR组分增强受细菌攻击的刺参体腔细胞吞噬作用。

miRNA-133 augments coelomocyte phagocytosis in bacteria-challenged Apostichopus japonicus via targeting the TLR component of IRAK-1 in vitro and in vivo.

作者信息

Lu Meng, Zhang Peng-Juan, Li Cheng-Hua, Lv Zhi-Meng, Zhang Wei-Wei, Jin Chun-Hua

机构信息

School of Marine Sciences, Ningbo University, Ningbo, Zhejiang Province 315211, P.R China.

出版信息

Sci Rep. 2015 Jul 30;5:12608. doi: 10.1038/srep12608.

Abstract

In this study, we explored the potential roles of miRNA-133 in regulating TLR pathways in the sea cucumber Apostichopus japonicus. Target screening of RNA-Seq data successfully identified interleukin-1 receptor-associated kinase (AjIRAK-1) as a putative target of miR-133. This result was further validated by negative expression profiles in Vibrio splendidus-challenged coelomocytes and lipopolysaccharide (LPS)-exposed cell cultures. HEK-293T cells transfected with a dual-luciferase reporter fused to the 3'UTR of wild-type or mutant AjIRAK-1 exhibited a 52.9% reduction in luciferase activity (p < 0.01) compared to controls. Co-infection with a miR-133 mimics or a specific siRNA targeting AjIRAK-1 significantly repressed the mRNA and protein expression levels of AjIRAK-1 and its downstream molecules, such as AjTRAF6 and Ajp105, in primary coelomocytes. In contrast, a miR-133 inhibitor significantly increased the expression of these TLR pathway members. The injection of miR-133 agomir or AjIRAK-1 siRNA into sea cucumbers not only decreased the expression of AjIRAK-1 and its downstream molecules but also significantly increased V. splendidus coelomocyte phagocytosis. All of the present data provide direct evidence that miR-133 is involved in TLR cascade modulation through AjIRAK-1 targeting to promote V. splendidus coelomocyte phagocytosis in these non-model invertebrates.

摘要

在本研究中,我们探讨了miRNA-133在调控刺参TLR通路中的潜在作用。通过对RNA-Seq数据进行靶标筛选,成功鉴定白细胞介素-1受体相关激酶(AjIRAK-1)为miR-133的假定靶标。在灿烂弧菌攻击的体腔细胞和暴露于脂多糖(LPS)的细胞培养物中的阴性表达谱进一步验证了这一结果。用与野生型或突变型AjIRAK-1的3'UTR融合的双荧光素酶报告基因转染的HEK-293T细胞,与对照相比,荧光素酶活性降低了52.9%(p < 0.01)。在原代体腔细胞中,与miR-133模拟物或靶向AjIRAK-1的特异性siRNA共感染显著抑制了AjIRAK-1及其下游分子(如AjTRAF6和Ajp105)的mRNA和蛋白表达水平。相反,miR-133抑制剂显著增加了这些TLR通路成员的表达。向刺参注射miR-133激动剂或AjIRAK-1 siRNA不仅降低了AjIRAK-1及其下游分子的表达,还显著增加了灿烂弧菌体腔细胞的吞噬作用。所有现有数据提供了直接证据,表明miR-133通过靶向AjIRAK-1参与TLR级联调节,以促进这些非模式无脊椎动物中灿烂弧菌体腔细胞的吞噬作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b8e/4519775/40a6eca1a3ab/srep12608-f1.jpg

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