• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.3389/fcimb.2022.934313
PMID:35903199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9315269/
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/fb9b9532bebf/fcimb-12-934313-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d6/9315269/7b155c35fb97/fcimb-12-934313-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d6/9315269/a8081225c80f/fcimb-12-934313-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d6/9315269/fb9b9532bebf/fcimb-12-934313-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d6/9315269/7b155c35fb97/fcimb-12-934313-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d6/9315269/a8081225c80f/fcimb-12-934313-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d6/9315269/fb9b9532bebf/fcimb-12-934313-g003.jpg

相似文献

1
The Long Non-Coding Antisense RNA JHDM1D-AS1 Regulates Inflammatory Responses in Human Monocytes.长非编码反义 RNA JHDM1D-AS1 调控人单核细胞炎症反应。
Front Cell Infect Microbiol. 2022 Jul 12;12:934313. doi: 10.3389/fcimb.2022.934313. eCollection 2022.
2
Upregulation of JHDM1D-AS1 alleviates neuroinflammation and neuronal injury via targeting miR-101-3p-DUSP1 in spinal cord after brachial plexus injury.JHDM1D-AS1 的上调通过靶向 miR-101-3p-DUSP1 减轻臂丛神经损伤后脊髓的神经炎症和神经元损伤。
Int Immunopharmacol. 2020 Dec;89(Pt A):106962. doi: 10.1016/j.intimp.2020.106962. Epub 2020 Oct 8.
3
LIN28B-AS1-IGF2BP1 association is required for LPS-induced NFκB activation and pro-inflammatory responses in human macrophages and monocytes.LIN28B-AS1-IGF2BP1 相互作用对于 LPS 诱导的人巨噬细胞和单核细胞中 NFκB 激活和促炎反应是必需的。
Biochem Biophys Res Commun. 2019 Nov 12;519(3):525-532. doi: 10.1016/j.bbrc.2019.09.012. Epub 2019 Sep 17.
4
LncRNA JHDM1D-AS1 Suppresses MPP + -Induced Neuronal Injury in Parkinson's Disease via miR-134-5p/PIK3R3 Axis.长链非编码 RNA JHDM1D-AS1 通过 miR-134-5p/PIK3R3 轴抑制帕金森病中 MPP+诱导的神经元损伤。
Neurotox Res. 2021 Dec;39(6):1771-1781. doi: 10.1007/s12640-021-00437-8. Epub 2021 Nov 13.
5
Long Non-coding RNA JHDM1D-AS1 Interacts with DHX15 Protein to Enhance Non-Small-Cell Lung Cancer Growth and Metastasis.长链非编码RNA JHDM1D-AS1与DHX15蛋白相互作用以促进非小细胞肺癌的生长和转移。
Mol Ther Nucleic Acids. 2019 Dec 6;18:831-840. doi: 10.1016/j.omtn.2019.09.028. Epub 2019 Oct 10.
6
Long Noncoding RNA JHDM1D-AS1 Promotes Tumor Growth by Regulating Angiogenesis in Response to Nutrient Starvation.长链非编码RNA JHDM1D-AS1通过调节血管生成对营养饥饿的反应来促进肿瘤生长。
Mol Cell Biol. 2017 Aug 28;37(18). doi: 10.1128/MCB.00125-17. Print 2017 Sep 15.
7
JHDM1D-AS1-driven inhibition of miR-940 releases ARTN expression to induce breast carcinogenesis.JHDM1D-AS1 驱动的 miR-940 抑制作用释放 ARTN 表达,从而诱导乳腺癌发生。
Clin Transl Oncol. 2023 Jul;25(7):2192-2203. doi: 10.1007/s12094-023-03102-y. Epub 2023 Mar 2.
8
Palmitic Acid-Induced Long Noncoding RNA Regulates Inflammation via Interaction With RNA-Binding Protein ELAVL1 in Monocytes and Macrophages.棕榈酸诱导的长非编码 RNA 通过与单核细胞和巨噬细胞中的 RNA 结合蛋白 ELAVL1 相互作用调节炎症。
Arterioscler Thromb Vasc Biol. 2023 Jul;43(7):1157-1175. doi: 10.1161/ATVBAHA.122.318536. Epub 2023 Apr 27.
9
LncRNA Is a Key Biomarker for Progression and Modulation of Gemcitabine Sensitivity in Bladder Cancer Cells.长链非编码 RNA 是膀胱癌细胞中吉西他滨敏感性进展和调节的关键生物标志物。
Molecules. 2023 Mar 6;28(5):2412. doi: 10.3390/molecules28052412.
10
Upregulation of JHDM1D-AS1 protects PDLSCs from HO-induced apoptosis by decreasing DNAJC10 via phosphorylation of eIF2α.JHDM1D-AS1 的上调通过磷酸化 eIF2α 降低 DNAJC10 来保护 PDLSCs 免受 HO 诱导的细胞凋亡。
Biochimie. 2019 Oct;165:48-56. doi: 10.1016/j.biochi.2019.06.018. Epub 2019 Jul 2.

引用本文的文献

1
Identification of key genes and development of an identifying machine learning model for sepsis.脓毒症关键基因的鉴定及识别机器学习模型的开发
Inflamm Res. 2025 Jun 30;74(1):100. doi: 10.1007/s00011-025-02068-7.
2
CRISPRi screen uncovers lncRNA regulators of human monocyte growth.CRISPR干扰筛选揭示人类单核细胞生长的长链非编码RNA调控因子。
J Biol Chem. 2025 May 7;301(6):110204. doi: 10.1016/j.jbc.2025.110204.
3
Advancing sepsis diagnosis and immunotherapy machine learning-driven identification of stable molecular biomarkers and therapeutic targets.

本文引用的文献

1
Web-based LinRegPCR: application for the visualization and analysis of (RT)-qPCR amplification and melting data.基于网络的 LinRegPCR:用于可视化和分析(RT)-qPCR 扩增和熔解数据的应用程序。
BMC Bioinformatics. 2021 Aug 24;22(1):398. doi: 10.1186/s12859-021-04306-1.
2
The long non-coding RNA LUCAT1 is a negative feedback regulator of interferon responses in humans.长非编码 RNA LUCAT1 是人类干扰素反应的负反馈调节因子。
Nat Commun. 2020 Dec 11;11(1):6348. doi: 10.1038/s41467-020-20165-5.
3
The leukocyte non-coding RNA landscape in critically ill patients with sepsis.
推进脓毒症诊断与免疫治疗:机器学习驱动的稳定分子生物标志物和治疗靶点识别
Sci Rep. 2025 Mar 11;15(1):8333. doi: 10.1038/s41598-025-93010-8.
4
KDM7A-DT induces genotoxic stress, tumorigenesis, and progression of p53 missense mutation-associated invasive breast cancer.KDM7A-DT诱导基因毒性应激、肿瘤发生以及与p53错义突变相关的浸润性乳腺癌的进展。
Front Oncol. 2024 May 2;14:1227151. doi: 10.3389/fonc.2024.1227151. eCollection 2024.
5
Salmonella manipulates the host to drive pathogenicity via induction of interleukin 1β.沙门氏菌通过诱导白细胞介素 1β来操纵宿主以促进发病。
PLoS Biol. 2024 Jan 18;22(1):e3002486. doi: 10.1371/journal.pbio.3002486. eCollection 2024 Jan.
6
Novel long non-coding RNAs associated with inflammation and macrophage activation in human.新型长链非编码 RNA 与人的炎症和巨噬细胞活化有关。
Sci Rep. 2023 Mar 10;13(1):4036. doi: 10.1038/s41598-023-30568-1.
危重症脓毒症患者白细胞非编码 RNA 图谱。
Elife. 2020 Dec 11;9:e58597. doi: 10.7554/eLife.58597.
4
Upregulation of JHDM1D-AS1 alleviates neuroinflammation and neuronal injury via targeting miR-101-3p-DUSP1 in spinal cord after brachial plexus injury.JHDM1D-AS1 的上调通过靶向 miR-101-3p-DUSP1 减轻臂丛神经损伤后脊髓的神经炎症和神经元损伤。
Int Immunopharmacol. 2020 Dec;89(Pt A):106962. doi: 10.1016/j.intimp.2020.106962. Epub 2020 Oct 8.
5
The circular RNA landscape in specific peripheral blood mononuclear cells of critically ill patients with sepsis.危重症脓毒症患者特定外周血单个核细胞中的环状 RNA 图谱。
Crit Care. 2020 Jul 13;24(1):423. doi: 10.1186/s13054-020-03146-4.
6
Long Non-coding RNA JHDM1D-AS1 Interacts with DHX15 Protein to Enhance Non-Small-Cell Lung Cancer Growth and Metastasis.长链非编码RNA JHDM1D-AS1与DHX15蛋白相互作用以促进非小细胞肺癌的生长和转移。
Mol Ther Nucleic Acids. 2019 Dec 6;18:831-840. doi: 10.1016/j.omtn.2019.09.028. Epub 2019 Oct 10.
7
Microglia Biology: One Century of Evolving Concepts.小胶质细胞生物学:百年演变概念。
Cell. 2019 Oct 3;179(2):292-311. doi: 10.1016/j.cell.2019.08.053.
8
Upregulation of JHDM1D-AS1 protects PDLSCs from HO-induced apoptosis by decreasing DNAJC10 via phosphorylation of eIF2α.JHDM1D-AS1 的上调通过磷酸化 eIF2α 降低 DNAJC10 来保护 PDLSCs 免受 HO 诱导的细胞凋亡。
Biochimie. 2019 Oct;165:48-56. doi: 10.1016/j.biochi.2019.06.018. Epub 2019 Jul 2.
9
The long noncoding RNA regulates CD8 T cells in response to viral infection.长非编码 RNA 调节病毒感染后 CD8 T 细胞的功能。
Proc Natl Acad Sci U S A. 2019 Jun 11;116(24):11916-11925. doi: 10.1073/pnas.1819457116. Epub 2019 May 28.
10
RNA-Seq Signatures Normalized by mRNA Abundance Allow Absolute Deconvolution of Human Immune Cell Types.RNA-Seq 特征通过 mRNA 丰度标准化可实现人类免疫细胞类型的绝对分解。
Cell Rep. 2019 Feb 5;26(6):1627-1640.e7. doi: 10.1016/j.celrep.2019.01.041.