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RIP2 敲低的鸡 HD11 巨噬细胞中长非编码 RNA 的表达谱与禽致病性大肠杆菌(APEC)感染相关。

Long noncoding RNAs expression profile of RIP2 knockdown in chicken HD11 macrophages associated with avian pathogenic E. coli (APEC) infection.

机构信息

College of Animal Science and Technology, Yangzhou University, Yangzhou, 225009, China.

College of Animal Science and Technology, Yangzhou University, Yangzhou, 225009, China; Joint International Research Laboratory of Agriculture & Agri-Product Safety, Ministry of Education, Yangzhou University, Yangzhou, 225009, China.

出版信息

Dev Comp Immunol. 2023 May;142:104650. doi: 10.1016/j.dci.2023.104650. Epub 2023 Feb 2.

Abstract

Avian pathogenic E. coli (APEC) has been detected to cause many acute and chronic diseases, resulting in huge economic losses to the poultry industry. Previous experiments have identified the effect of receptor interacting serine/threonine kinase 2 (RIP2) gene in APEC infection. Moreover, increasing evidence indicates that long noncoding RNAs (lncRNAs) play important roles in the anti-bacteria responses. However, little is known about the functions of lncRNAs, especially related to RIP2, in response to APEC. Therefore, we tried to reveal lncRNAs potentially involved in the immune and inflammatory response against APEC infection, with a particular focus on those possibly correlated with RIP2. A total of 1856 and 1373 differentially expressed (DE) lncRNAs were identified in knockdown of RIP2 cells following APEC infection (shRIP2+APEC) vs. APEC and shRIP2 vs. wild type cells (WT), respectively, which were mainly enriched in lysosome, phagosome, NOD-like receptor signaling pathway, TGF-beta signaling pathway. Significantly, TCONS_00009695 regulated by RIP2 could directly alter the expression of target BIRC3 to modulate cytokines and to participate in immune and inflammatory response against APEC infection. Our findings aid to a better understanding of host responses to APEC infection and provide new directions for understanding the potential association between lncRNAs and APEC pathogenesis.

摘要

禽致病性大肠杆菌(APEC)已被发现可引起许多急性和慢性疾病,给家禽业造成巨大的经济损失。先前的实验已经确定了受体相互作用丝氨酸/苏氨酸激酶 2(RIP2)基因在 APEC 感染中的作用。此外,越来越多的证据表明,长链非编码 RNA(lncRNA)在抗菌反应中发挥重要作用。然而,人们对 lncRNA 的功能知之甚少,特别是与 RIP2 相关的功能,在应对 APEC 方面。因此,我们试图揭示 lncRNA 可能参与针对 APEC 感染的免疫和炎症反应,特别关注那些可能与 RIP2 相关的 lncRNA。在 RIP2 敲低细胞感染 APEC(shRIP2+APEC)与 APEC 和 RIP2 敲低细胞(WT)相比,分别鉴定出 1856 个和 1373 个差异表达(DE)lncRNA,它们主要富集在溶酶体、吞噬体、NOD 样受体信号通路、TGF-β信号通路。值得注意的是,由 RIP2 调节的 TCONS_00009695 可以直接改变靶基因 BIRC3 的表达,从而调节细胞因子,并参与针对 APEC 感染的免疫和炎症反应。我们的研究结果有助于更好地理解宿主对 APEC 感染的反应,并为理解 lncRNA 与 APEC 发病机制之间的潜在关联提供了新的方向。

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