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长非编码反义 RNA JHDM1D-AS1 调控人单核细胞炎症反应。

The Long Non-Coding Antisense RNA JHDM1D-AS1 Regulates Inflammatory Responses in Human Monocytes.

机构信息

Amsterdam University Medical Centers, Center for Experimental and Molecular Medicine, University of Amsterdam, Amsterdam, Netherlands.

Division of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.

出版信息

Front Cell Infect Microbiol. 2022 Jul 12;12:934313. doi: 10.3389/fcimb.2022.934313. eCollection 2022.

Abstract

Monocytes are key players in innate immunity, with their ability to regulate inflammatory responses and combat invading pathogens. There is a growing body of evidence indicating that long non-coding RNA (lncRNA) participate in various cellular biological processes, including the innate immune response. The immunoregulatory properties of numerous lncRNAs discovered in monocytes remain largely unexplored. Here, by RNA sequencing, we identified a lncRNA JHDM1D-AS1, which was upregulated in blood monocytes obtained from patients with sepsis relative to healthy controls. expression was induced in primary human monocytes exposed to Toll-like receptor ligands, such as lipopolysaccharide (LPS), or bacteria. The inducibility of expression in monocytes depended, at least in part, on nuclear factor-κB activation. JHDM1D-AS1 knockdown experiments in human monocyte-derived macrophages revealed significantly enhanced expression of inflammatory mediators, before and after exposure to LPS, relative to control cells. Specifically, genes involved in inflammatory responses were upregulated (e.g., , , , , , and ), whereas genes involved in anti-inflammatory pathways were downregulated (e.g., and ). overexpression in a pro-monocytic cell line revealed diminished pro-inflammatory responses subsequent to LPS challenge. Collectively, these findings identify as a potential anti-inflammatory mediator induced in response to inflammatory stimuli.

摘要

单核细胞是先天免疫的关键参与者,具有调节炎症反应和抵御入侵病原体的能力。越来越多的证据表明,长非编码 RNA(lncRNA)参与各种细胞生物学过程,包括先天免疫反应。单核细胞中发现的许多 lncRNA 的免疫调节特性在很大程度上仍未得到探索。在这里,我们通过 RNA 测序鉴定了一个 lncRNA JHDM1D-AS1,它在脓毒症患者的血液单核细胞中相对于健康对照上调。在暴露于 Toll 样受体配体(如脂多糖(LPS)或细菌)的原代人单核细胞中诱导表达。单核细胞中表达的诱导至少部分取决于核因子-κB 的激活。在人单核细胞衍生的巨噬细胞中进行 JHDM1D-AS1 敲低实验后,与对照细胞相比,在暴露于 LPS 前后,炎症介质的表达显著增强。具体而言,参与炎症反应的基因上调(例如, 、 、 、 、 和 ),而参与抗炎途径的基因下调(例如 和 )。在促单核细胞系中的过表达表明,在 LPS 挑战后,促炎反应减弱。总之,这些发现表明 作为一种潜在的抗炎介质,可响应炎症刺激诱导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d6/9315269/7b155c35fb97/fcimb-12-934313-g001.jpg

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