• 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

ILC3s 限制肠道细菌的传播,以保护手术后的肝脏再生。

ILC3s restrict the dissemination of intestinal bacteria to safeguard liver regeneration after surgery.

机构信息

Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland; Institute of Microbiology, Infectious Diseases and Immunology (I-MIDI), Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.

Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

出版信息

Cell Rep. 2023 Mar 28;42(3):112269. doi: 10.1016/j.celrep.2023.112269. Epub 2023 Mar 17.

DOI:10.1016/j.celrep.2023.112269
PMID:36933213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10066576/
Abstract

It is generally believed that environmental or cutaneous bacteria are the main origin of surgical infections. Therefore, measures to prevent postoperative infections focus on optimizing hygiene and improving asepsis and antisepsis. In a large cohort of patients with infections following major surgery, we identified that the causative bacteria are mainly of intestinal origin. Postoperative infections of intestinal origin were also found in mice undergoing partial hepatectomy. CCR6 group 3 innate lymphoid cells (ILC3s) limited systemic bacterial spread. Such bulwark function against host invasion required the production of interleukin-22 (IL-22), which controlled the expression of antimicrobial peptides in hepatocytes, thereby limiting bacterial spread. Using genetic loss-of-function experiments and punctual depletion of ILCs, we demonstrate that the failure to restrict intestinal commensals by ILC3s results in impaired liver regeneration. Our data emphasize the importance of endogenous intestinal bacteria as a source for postoperative infection and indicate ILC3s as potential new targets.

摘要

人们普遍认为环境或皮肤细菌是外科感染的主要来源。因此,预防术后感染的措施主要集中在优化卫生和提高无菌和消毒水平上。在一项对主要手术后感染患者的大型队列研究中,我们发现病原体主要来源于肠道。在接受部分肝切除术的小鼠中也发现了源自肠道的术后感染。CCR6 组 3 固有淋巴细胞(ILC3)可限制全身细菌扩散。这种抵御宿主入侵的堡垒功能需要白细胞介素 22(IL-22)的产生,它控制了肝细胞中抗菌肽的表达,从而限制了细菌的扩散。通过遗传功能丧失实验和 ILC 的定点耗竭,我们证明了 ILC3 无法限制肠道共生菌会导致肝再生受损。我们的数据强调了内源性肠道细菌作为术后感染源的重要性,并表明 ILC3 是潜在的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/c2d97915e53e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/7984d84d486d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/99c2106bd724/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/5f0a2f431c0a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/e1d2889ebefd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/9c1f21be6922/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/1a5510968570/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/c2d97915e53e/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/7984d84d486d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/99c2106bd724/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/5f0a2f431c0a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/e1d2889ebefd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/9c1f21be6922/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/1a5510968570/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f35/10066576/c2d97915e53e/gr6.jpg

相似文献

1
ILC3s restrict the dissemination of intestinal bacteria to safeguard liver regeneration after surgery.ILC3s 限制肠道细菌的传播,以保护手术后的肝脏再生。
Cell Rep. 2023 Mar 28;42(3):112269. doi: 10.1016/j.celrep.2023.112269. Epub 2023 Mar 17.
2
Sirtuin 6 inhibits group 3 innate lymphoid cell function and gut immunity by suppressing IL-22 production.Sirtuin 6 通过抑制 IL-22 的产生来抑制第三类固有淋巴细胞的功能和肠道免疫。
Front Immunol. 2024 Aug 26;15:1402834. doi: 10.3389/fimmu.2024.1402834. eCollection 2024.
3
Heterogeneity and diversity of group 3 innate lymphoid cells: new cells on the block.3型固有淋巴细胞的异质性与多样性:免疫细胞新成员
Int Immunol. 2016 Jan;28(1):29-34. doi: 10.1093/intimm/dxv054. Epub 2015 Oct 13.
4
Commensal and Pathogenic Bacteria Indirectly Induce IL-22 but Not IFNγ Production From Human Colonic ILC3s via Multiple Mechanisms.共生菌和致病菌通过多种机制间接诱导人结肠固有层内淋巴细胞 3 型(ILC3)产生白细胞介素 22(IL-22),但不产生干扰素 γ(IFNγ)。
Front Immunol. 2019 Mar 29;10:649. doi: 10.3389/fimmu.2019.00649. eCollection 2019.
5
AhR ligands from metabolites promote piglet intestinal ILC3 activation and IL-22 secretion to inhibit PEDV infection.来自代谢产物的芳烃受体配体可促进仔猪肠道3型固有淋巴细胞激活及白细胞介素-22分泌,以抑制猪流行性腹泻病毒感染。
J Virol. 2024 Aug 20;98(8):e0103924. doi: 10.1128/jvi.01039-24. Epub 2024 Jul 16.
6
Group 3 innate lymphoid cells (ILC3s): Origin, differentiation, and plasticity in humans and mice.第3组固有淋巴细胞(ILC3s):人类和小鼠中的起源、分化及可塑性
Eur J Immunol. 2015 Aug;45(8):2171-82. doi: 10.1002/eji.201545598. Epub 2015 Jun 18.
7
IL-18-induced HIF-1α in ILC3s ameliorates the inflammation of C. rodentium-induced colitis.IL-18 诱导 ILC3 中的 HIF-1α 减轻 C. rodentium 诱导的结肠炎的炎症。
Cell Rep. 2023 Dec 26;42(12):113508. doi: 10.1016/j.celrep.2023.113508. Epub 2023 Nov 28.
8
Adoptive Transfer of Group 3-Like Innate Lymphoid Cells Restores Mouse Colon Resistance to Colonization of a Gamma Interferon-Susceptible Chlamydia muridarum Mutant. adoptive transfer of group 3-like innate lymphoid cells restores mouse colon resistance to colonization of a gamma interferon-susceptible chlamydia muridarum mutant.
Infect Immun. 2021 Jan 19;89(2). doi: 10.1128/IAI.00533-20.
9
The role of the aryl hydrocarbon receptor (AhR) in modulating intestinal ILC3s to optimise gut pathogen resistance in lupus and benefits of nutritional AhR ligands.芳烃受体(AhR)在调节肠道3型固有淋巴细胞(ILC3s)以优化狼疮中肠道病原体抵抗力方面的作用以及营养性AhR配体的益处。
Clin Nutr. 2024 Jun;43(6):1199-1215. doi: 10.1016/j.clnu.2024.04.008. Epub 2024 Apr 8.
10
Intermittent fasting promotes type 3 innate lymphoid cells secreting IL-22 contributing to the beigeing of white adipose tissue.间歇性禁食促进 3 型先天淋巴样细胞分泌 IL-22,促进白色脂肪组织的米色化。
Elife. 2024 Mar 27;12:RP91060. doi: 10.7554/eLife.91060.

引用本文的文献

1
The formidable guardian: Type 3 immunity in the intestine of pigs.强大的守护者:猪肠道中的 3 型免疫。
Virulence. 2024 Dec;15(1):2424325. doi: 10.1080/21505594.2024.2424325. Epub 2024 Nov 8.
2
Bridging Chronic Inflammation and Digestive Cancer: The Critical Role of Innate Lymphoid Cells in Tumor Microenvironments.桥接慢性炎症与消化道癌症:固有淋巴细胞在肿瘤微环境中的关键作用。
Int J Biol Sci. 2024 Sep 9;20(12):4799-4818. doi: 10.7150/ijbs.96338. eCollection 2024.
3
The role of trained immunity in sepsis.训练免疫在脓毒症中的作用。

本文引用的文献

1
Programing of an Intravascular Immune Firewall by the Gut Microbiota Protects against Pathogen Dissemination during Infection.肠道微生物群通过编程形成血管内免疫防火墙,防止感染期间病原体传播。
Cell Host Microbe. 2020 Nov 11;28(5):660-668.e4. doi: 10.1016/j.chom.2020.07.014. Epub 2020 Aug 17.
2
Innate lymphoid cells control signaling circuits to regulate tissue-specific immunity.先天淋巴细胞控制信号通路以调节组织特异性免疫。
Cell Res. 2020 Jun;30(6):475-491. doi: 10.1038/s41422-020-0323-8. Epub 2020 May 6.
3
Immunoregulatory Sensory Circuits in Group 3 Innate Lymphoid Cell (ILC3) Function and Tissue Homeostasis.
Front Immunol. 2024 Aug 15;15:1449986. doi: 10.3389/fimmu.2024.1449986. eCollection 2024.
4
Antimicrobial Peptides (AMPs) and the Microbiome in Preterm Infants: Consequences and Opportunities for Future Therapeutics.抗菌肽 (AMPs) 和早产儿微生物组:未来治疗的后果和机遇。
Int J Mol Sci. 2024 Jun 18;25(12):6684. doi: 10.3390/ijms25126684.
5
IL-33 controls IL-22-dependent antibacterial defense by modulating the microbiota.IL-33 通过调节微生物群来控制 IL-22 依赖的抗菌防御。
Proc Natl Acad Sci U S A. 2024 May 28;121(22):e2310864121. doi: 10.1073/pnas.2310864121. Epub 2024 May 23.
免疫调节感应回路在 3 组固有淋巴细胞(ILC3)功能和组织动态平衡中的作用
Front Immunol. 2020 Feb 6;11:116. doi: 10.3389/fimmu.2020.00116. eCollection 2020.
4
Feeding-dependent VIP neuron-ILC3 circuit regulates the intestinal barrier.进食依赖的 VIP 神经元-ILC3 回路调节肠道屏障。
Nature. 2020 Mar;579(7800):575-580. doi: 10.1038/s41586-020-2039-9. Epub 2020 Feb 12.
5
The gut-liver axis in liver disease: Pathophysiological basis for therapy.肝脏疾病中的肠-肝轴:治疗的病理生理学基础。
J Hepatol. 2020 Mar;72(3):558-577. doi: 10.1016/j.jhep.2019.10.003. Epub 2019 Oct 14.
6
Association Between Preoperative Muscle Mass and Intraoperative Bacterial Translocation in Patients Undergoing Hepatectomy, Pancreatoduodenectomy, and Esophagectomy.肝切除术、胰十二指肠切除术和食管癌切除术患者术前肌肉量与术中细菌易位的关系。
Ann Surg Oncol. 2019 Dec;26(13):4805-4813. doi: 10.1245/s10434-019-07707-y. Epub 2019 Aug 12.
7
Epithelial Indoleamine 2,3-Dioxygenase 1 Modulates Aryl Hydrocarbon Receptor and Notch Signaling to Increase Differentiation of Secretory Cells and Alter Mucus-Associated Microbiota.上皮型色氨酸 2,3-双加氧酶 1 调节芳香烃受体和 Notch 信号通路以增加分泌细胞的分化,并改变与黏液相关的微生物群。
Gastroenterology. 2019 Oct;157(4):1093-1108.e11. doi: 10.1053/j.gastro.2019.07.013. Epub 2019 Jul 17.
8
FXR modulates the gut-vascular barrier by regulating the entry sites for bacterial translocation in experimental cirrhosis.FXR 通过调节实验性肝硬化中细菌易位的进入部位来调节肠道-血管屏障。
J Hepatol. 2019 Dec;71(6):1126-1140. doi: 10.1016/j.jhep.2019.06.017. Epub 2019 Jul 8.
9
Interleukin-22 protects intestinal stem cells against genotoxic stress.白细胞介素-22 可保护肠道干细胞免受遗传毒性应激。
Nature. 2019 Feb;566(7743):249-253. doi: 10.1038/s41586-019-0899-7. Epub 2019 Jan 30.
10
Microbial network disturbances in relapsing refractory Crohn's disease.复发缓解型和难治性克罗恩病中的微生物网络紊乱
Nat Med. 2019 Feb;25(2):323-336. doi: 10.1038/s41591-018-0308-z. Epub 2019 Jan 21.