• 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

相似文献

1
Host-microbiota interactions: epigenomic regulation.宿主-微生物群相互作用:表观基因组调控
Curr Opin Immunol. 2017 Feb;44:52-60. doi: 10.1016/j.coi.2016.12.001. Epub 2017 Jan 16.
2
Epigenomic regulation of host-microbiota interactions.宿主-微生物群相互作用的表观基因组调控
Trends Immunol. 2014 Nov;35(11):518-25. doi: 10.1016/j.it.2014.09.007. Epub 2014 Oct 22.
3
Dietary metabolites derived from gut microbiota: critical modulators of epigenetic changes in mammals.源自肠道微生物群的膳食代谢产物:哺乳动物表观遗传变化的关键调节因子。
Nutr Rev. 2017 May 1;75(5):374-389. doi: 10.1093/nutrit/nux001.
4
Epigenomics and the microbiota.表观基因组学与微生物群
Toxicol Pathol. 2015 Jan;43(1):101-6. doi: 10.1177/0192623314553805. Epub 2014 Oct 20.
5
Chromatin dynamics and histone modifications in intestinal microbiota-host crosstalk.肠道微生物群-宿主互作中的染色质动态和组蛋白修饰。
Mol Metab. 2020 Aug;38:100925. doi: 10.1016/j.molmet.2019.12.005. Epub 2019 Dec 27.
6
Integration of microbiome and epigenome to decipher the pathogenesis of autoimmune diseases.整合微生物组和表观基因组以破解自身免疫性疾病的发病机制。
J Autoimmun. 2017 Sep;83:31-42. doi: 10.1016/j.jaut.2017.03.009. Epub 2017 Mar 23.
7
The effects of commensal microbiota on immune cell subsets and inflammatory responses.共生微生物群对免疫细胞亚群和炎症反应的影响。
Immunol Rev. 2012 Jan;245(1):45-55. doi: 10.1111/j.1600-065X.2011.01083.x.
8
Microbiota-Derived Short-Chain Fatty Acids Modulate Expression of Determinants Required for Commensalism and Virulence.微生物群衍生的短链脂肪酸调节共生和毒力所需决定因素的表达。
mBio. 2017 May 9;8(3):e00407-17. doi: 10.1128/mBio.00407-17.
9
Microbiota-derived metabolite promotes HDAC3 activity in the gut.肠道微生物衍生代谢物促进 HDAC3 活性。
Nature. 2020 Oct;586(7827):108-112. doi: 10.1038/s41586-020-2604-2. Epub 2020 Jul 30.
10
Regulation of bacterial pathogenesis by intestinal short-chain Fatty acids.肠道短链脂肪酸对细菌致病性的调控
Adv Appl Microbiol. 2013;85:93-118. doi: 10.1016/B978-0-12-407672-3.00003-4.

引用本文的文献

1
Epigenetic modifications of gut microbiota and their potential role in atherosclerosis.肠道微生物群的表观遗传修饰及其在动脉粥样硬化中的潜在作用。
Front Pharmacol. 2025 Jul 16;16:1638240. doi: 10.3389/fphar.2025.1638240. eCollection 2025.
2
The role of probiotics in promoting systemic immune tolerance in systemic lupus erythematosus.益生菌在促进系统性红斑狼疮患者全身免疫耐受中的作用。
Gut Pathog. 2025 Jun 17;17(1):45. doi: 10.1186/s13099-025-00702-7.
3
Interaction between the breast tumor microenvironment and gut microbiome.乳腺肿瘤微环境与肠道微生物群之间的相互作用。
Gut Microbes. 2025 Dec;17(1):2514136. doi: 10.1080/19490976.2025.2514136. Epub 2025 Jun 8.
4
The microbiota: a crucial mediator in gut homeostasis and colonization resistance.微生物群:肠道稳态和定植抗性的关键调节因子。
Front Microbiol. 2024 Aug 6;15:1417864. doi: 10.3389/fmicb.2024.1417864. eCollection 2024.
5
Gut microbiota and epigenetic choreography: Implications for human health: A review.肠道微生物群与表观遗传协调:对人类健康的影响:综述。
Medicine (Baltimore). 2024 Jul 19;103(29):e39051. doi: 10.1097/MD.0000000000039051.
6
Vitamin D: An Essential Nutrient in the Dual Relationship between Autoimmune Thyroid Diseases and Celiac Disease-A Comprehensive Review.维生素 D:在自身免疫性甲状腺疾病和乳糜泻的双重关系中不可或缺的营养物质——全面综述
Nutrients. 2024 Jun 4;16(11):1762. doi: 10.3390/nu16111762.
7
Xiaoqinglong decoction mitigates nasal inflammation and modulates gut microbiota in allergic rhinitis mice.小青龙汤减轻变应性鼻炎小鼠的鼻腔炎症并调节肠道微生物群。
Front Microbiol. 2024 May 15;15:1290985. doi: 10.3389/fmicb.2024.1290985. eCollection 2024.
8
Potential Molecular Mechanisms of Alcohol Use Disorder with Non-Coding RNAs and Gut Microbiota for the Development of Superior Therapeutic Application.酒精使用障碍与非编码RNA和肠道微生物群在开发高级治疗应用方面的潜在分子机制
Genes (Basel). 2024 Mar 29;15(4):431. doi: 10.3390/genes15040431.
9
Intestinal microbiota regulates the gut-thyroid axis: the new dawn of improving Hashimoto thyroiditis.肠道微生物群调节肠道-甲状腺轴:改善桥本甲状腺炎的新曙光。
Clin Exp Med. 2024 Feb 22;24(1):39. doi: 10.1007/s10238-024-01304-4.
10
The Effects of Environmental Exposure on Epigenetic Modifications in Allergic Diseases.环境暴露对过敏性疾病中表观遗传修饰的影响。
Medicina (Kaunas). 2024 Jan 7;60(1):110. doi: 10.3390/medicina60010110.

本文引用的文献

1
Gut Microbiota: A Contributing Factor to Obesity.肠道微生物群:肥胖的一个促成因素。
Front Cell Infect Microbiol. 2016 Aug 30;6:95. doi: 10.3389/fcimb.2016.00095. eCollection 2016.
2
The Spectrum and Regulatory Landscape of Intestinal Innate Lymphoid Cells Are Shaped by the Microbiome.肠道固有淋巴细胞的谱和调控景观受微生物组的影响。
Cell. 2016 Aug 25;166(5):1231-1246.e13. doi: 10.1016/j.cell.2016.07.043. Epub 2016 Aug 18.
3
β8 Integrin Expression and Activation of TGF-β by Intestinal Dendritic Cells Are Determined by Both Tissue Microenvironment and Cell Lineage.肠道树突状细胞的β8整合素表达及TGF-β激活由组织微环境和细胞谱系共同决定。
J Immunol. 2016 Sep 1;197(5):1968-78. doi: 10.4049/jimmunol.1600244. Epub 2016 Aug 1.
4
Role of Serum Amyloid A, Granulocyte-Macrophage Colony-Stimulating Factor, and Bone Marrow Granulocyte-Monocyte Precursor Expansion in Segmented Filamentous Bacterium-Mediated Protection from Entamoeba histolytica.血清淀粉样蛋白A、粒细胞-巨噬细胞集落刺激因子和骨髓粒细胞-单核细胞前体扩增在分节丝状菌介导的对溶组织内阿米巴的保护作用中的角色。
Infect Immun. 2016 Sep 19;84(10):2824-32. doi: 10.1128/IAI.00316-16. Print 2016 Oct.
5
Epigenetic control of adult stem cell function.表观遗传学对成体干细胞功能的调控。
Nat Rev Mol Cell Biol. 2016 Oct;17(10):643-58. doi: 10.1038/nrm.2016.76. Epub 2016 Jul 13.
6
A Novel Allosteric Activator of Free Fatty Acid 2 Receptor Displays Unique Gi-functional Bias.游离脂肪酸2受体的新型变构激活剂表现出独特的Gi功能偏向性。
J Biol Chem. 2016 Sep 2;291(36):18915-31. doi: 10.1074/jbc.M116.736157. Epub 2016 Jul 5.
7
The microbiome and innate immunity.微生物组与先天免疫。
Nature. 2016 Jul 7;535(7610):65-74. doi: 10.1038/nature18847.
8
Development of innate lymphoid cells.先天淋巴细胞的发育。
Nat Immunol. 2016 Jun 21;17(7):775-82. doi: 10.1038/ni.3481.
9
The Colonic Crypt Protects Stem Cells from Microbiota-Derived Metabolites.结肠隐窝保护干细胞免受微生物群衍生代谢物的影响。
Cell. 2016 Jun 16;165(7):1708-1720. doi: 10.1016/j.cell.2016.05.018. Epub 2016 Jun 2.
10
Gut microbiota, metabolites and host immunity.肠道微生物群、代谢产物与宿主免疫
Nat Rev Immunol. 2016 May 27;16(6):341-52. doi: 10.1038/nri.2016.42.

宿主-微生物群相互作用:表观基因组调控

Host-microbiota interactions: epigenomic regulation.

作者信息

Woo Vivienne, Alenghat Theresa

机构信息

Division of Immunobiology, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.

Division of Immunobiology, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.

出版信息

Curr Opin Immunol. 2017 Feb;44:52-60. doi: 10.1016/j.coi.2016.12.001. Epub 2017 Jan 16.

DOI:10.1016/j.coi.2016.12.001
PMID:28103497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5451311/
Abstract

The coevolution of mammalian hosts and their commensal microbiota has led to the development of complex symbiotic relationships between resident microbes and mammalian cells. Epigenomic modifications enable host cells to alter gene expression without modifying the genetic code, and therefore represent potent mechanisms by which mammalian cells can transcriptionally respond, transiently or stably, to environmental cues. Advances in genome-wide approaches are accelerating our appreciation of microbial influences on host physiology, and increasing evidence highlights that epigenomics represent a level of regulation by which the host integrates and responds to microbial signals. In particular, bacterial-derived short chain fatty acids have emerged as one clear link between how the microbiota intersects with host epigenomic pathways. Here we review recent findings describing crosstalk between the microbiota and epigenomic pathways in multiple mammalian cell populations. Further, we discuss interesting links that suggest that the scope of our understanding of epigenomic regulation in the host-microbiota relationship is still in its infancy.

摘要

哺乳动物宿主与其共生微生物群的共同进化导致了常驻微生物与哺乳动物细胞之间复杂共生关系的发展。表观基因组修饰使宿主细胞能够在不改变遗传密码的情况下改变基因表达,因此代表了哺乳动物细胞可以对环境线索进行瞬时或稳定转录反应的有效机制。全基因组方法的进展正在加速我们对微生物对宿主生理学影响的认识,越来越多的证据表明表观基因组学代表了宿主整合和响应微生物信号的一种调节水平。特别是,细菌衍生的短链脂肪酸已成为微生物群与宿主表观基因组途径相互作用的一个明显联系。在这里,我们回顾了最近描述微生物群与多个哺乳动物细胞群体中表观基因组途径之间相互作用的研究结果。此外,我们讨论了一些有趣的联系,这些联系表明我们对宿主-微生物群关系中表观基因组调节的理解仍处于起步阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7955/5451311/bc4902ee7173/nihms839249f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7955/5451311/7580f75d279b/nihms839249f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7955/5451311/bc4902ee7173/nihms839249f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7955/5451311/7580f75d279b/nihms839249f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7955/5451311/bc4902ee7173/nihms839249f2.jpg