Suppr超能文献

诱导长非编码 RNA 转录本 NR_045064 促进防御基因转录并有助于肠道上皮细胞对 感染的反应。

Induction of a Long Noncoding RNA Transcript, NR_045064, Promotes Defense Gene Transcription and Facilitates Intestinal Epithelial Cell Responses against Infection.

机构信息

Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, NE 68178.

Research Division of Immunology, Department of Medicine, Cedars-Sinai Medical Center, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90048.

出版信息

J Immunol. 2018 Dec 15;201(12):3630-3640. doi: 10.4049/jimmunol.1800566. Epub 2018 Nov 16.

Abstract

is an important opportunistic intestinal pathogen for immunocompromised individuals and a common cause of diarrhea in young children in developing countries. Gastrointestinal epithelial cells play a central role in activating and orchestrating host immune responses against infection, but underlying molecular mechanisms are not fully understood. We report in this paper that infection causes significant alterations in long noncoding RNA (lncRNA) expression profiles in murine intestinal epithelial cells. Transcription of a panel of lncRNA genes, including , in infected cells is controlled by the NF-κB signaling. Functionally, inhibition of NR_045064 induction increases parasite burden in intestinal epithelial cells. Induction of NR_045064 enhances the transcription of selected defense genes in host cells following infection. Epigenetic histone modifications are involved in NR_045064-mediated transcription of associated defense genes in infected host cells. Moreover, the p300/MLL-associated chromatin remodeling is involved in NR_045064-mediated transcription of associated defense genes in intestinal epithelial cells following infection. Expression of NR_045064 and associated genes is also identified in intestinal epithelium in C57BL/6J mice following phosphorothioate oligodeoxynucleotide or LPS stimulation. Our data demonstrate that lncRNAs, such as NR_045064, play a role in regulating epithelial defense against microbial infection.

摘要

是免疫功能低下个体的重要机会性肠道病原体,也是发展中国家幼儿腹泻的常见病因。胃肠道上皮细胞在激活和协调宿主对感染的免疫反应方面发挥着核心作用,但潜在的分子机制尚不完全清楚。我们在本文中报道,感染导致小鼠肠道上皮细胞中长非编码 RNA(lncRNA)表达谱发生显著改变。一组 lncRNA 基因,包括 ,在感染细胞中的转录受 NF-κB 信号的控制。功能上,抑制 NR_045064 的诱导会增加肠道上皮细胞中的寄生虫负担。NR_045064 的诱导增强了宿主细胞在感染后对选定防御基因的转录。表观遗传组蛋白修饰参与感染宿主细胞中 NR_045064 介导的相关防御基因的转录。此外,p300/MLL 相关染色质重塑参与感染后肠道上皮细胞中 NR_045064 介导的相关防御基因的转录。在 C57BL/6J 小鼠用硫代磷酸寡脱氧核苷酸或 LPS 刺激后,也在肠上皮细胞中检测到 NR_045064 和相关基因的表达。我们的数据表明,lncRNA 如 NR_045064,在调节上皮防御微生物感染方面发挥作用。

相似文献

5
hijacks a host's long noncoding RNA U90926 to evade intestinal epithelial cell-autonomous antiparasitic defense.
Front Immunol. 2023 Jun 5;14:1205468. doi: 10.3389/fimmu.2023.1205468. eCollection 2023.
7
Interferon-λ3 Promotes Epithelial Defense and Barrier Function Against Cryptosporidium parvum Infection.
Cell Mol Gastroenterol Hepatol. 2019;8(1):1-20. doi: 10.1016/j.jcmgh.2019.02.007. Epub 2019 Mar 5.
9
mA mRNA Methylation Regulates Epithelial Innate Antimicrobial Defense Against Cryptosporidial Infection.
Front Immunol. 2021 Jul 6;12:705232. doi: 10.3389/fimmu.2021.705232. eCollection 2021.

引用本文的文献

1
LncRNA BACE1-AS delays the propagation of through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis.
Microbiol Spectr. 2025 Jul;13(7):e0202224. doi: 10.1128/spectrum.02022-24. Epub 2025 Jun 9.
2
Molecular pathogenesis of Cryptosporidium and advancements in therapeutic interventions.
Parasite. 2025;32:7. doi: 10.1051/parasite/2025001. Epub 2025 Feb 4.
4
Unveiling the Hidden Regulators: The Impact of lncRNAs on Zoonoses.
Int J Mol Sci. 2024 Mar 21;25(6):3539. doi: 10.3390/ijms25063539.
5
infection alters the intestinal mucosa transcriptome in neonatal calves: implications for immune function.
Front Immunol. 2024 Jan 22;15:1351427. doi: 10.3389/fimmu.2024.1351427. eCollection 2024.
6
hijacks a host's long noncoding RNA U90926 to evade intestinal epithelial cell-autonomous antiparasitic defense.
Front Immunol. 2023 Jun 5;14:1205468. doi: 10.3389/fimmu.2023.1205468. eCollection 2023.
8
Whole transcriptome analysis of HCT-8 cells infected by Cryptosporidium parvum.
Parasit Vectors. 2022 Nov 24;15(1):441. doi: 10.1186/s13071-022-05565-4.

本文引用的文献

1
A Map of Toll-like Receptor Expression in the Intestinal Epithelium Reveals Distinct Spatial, Cell Type-Specific, and Temporal Patterns.
Immunity. 2018 Sep 18;49(3):560-575.e6. doi: 10.1016/j.immuni.2018.07.016. Epub 2018 Aug 28.
2
Identification of a Predominantly Interferon-λ-Induced Transcriptional Profile in Murine Intestinal Epithelial Cells.
Front Immunol. 2017 Oct 16;8:1302. doi: 10.3389/fimmu.2017.01302. eCollection 2017.
4
Genome-scale activation screen identifies a lncRNA locus regulating a gene neighbourhood.
Nature. 2017 Aug 17;548(7667):343-346. doi: 10.1038/nature23451. Epub 2017 Aug 11.
5
Intervention of Dietary Dipeptide Gamma-l-Glutamyl-l-Valine (γ-EV) Ameliorates Inflammatory Response in a Mouse Model of LPS-Induced Sepsis.
J Agric Food Chem. 2017 Jul 26;65(29):5953-5960. doi: 10.1021/acs.jafc.7b02109. Epub 2017 Jul 10.
6
MLL3/MLL4 are required for CBP/p300 binding on enhancers and super-enhancer formation in brown adipogenesis.
Nucleic Acids Res. 2017 Jun 20;45(11):6388-6403. doi: 10.1093/nar/gkx234.
10
Methyltransferase-like protein 16 binds the 3'-terminal triple helix of MALAT1 long noncoding RNA.
Proc Natl Acad Sci U S A. 2016 Dec 6;113(49):14013-14018. doi: 10.1073/pnas.1614759113. Epub 2016 Nov 21.

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