• 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

引流小肠和结肠的淋巴结在解剖学上是分开的,在免疫学上也是不同的。

The lymph nodes draining the small intestine and colon are anatomically separate and immunologically distinct.

作者信息

Houston S A, Cerovic V, Thomson C, Brewer J, Mowat A M, Milling S

机构信息

Centre for Immunobiology, Institute for Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.

出版信息

Mucosal Immunol. 2016 Mar;9(2):468-78. doi: 10.1038/mi.2015.77. Epub 2015 Sep 2.

DOI:10.1038/mi.2015.77
PMID:26329428
Abstract

Dendritic cells (DCs) in the small intestine (SI) and colon are fundamental to direct intestinal immune responses; they migrate to the mesenteric lymph nodes (MLNs) and prime T cells. We demonstrate anatomical segregation of lymphatic drainage from the intestine, specifically that DCs from the SI and colon migrate to different nodes within the MLN, here called the sMLN and cMLN. As a consequence, different frequencies of DC subsets observed in the SI and colon are reflected among the DCs in the sMLN and cMLN. Consistent with the SI's function in absorbing food, fed antigen is presented in the sMLN, but not in the cMLN. Furthermore, the levels of expression of CCR9 and α4β7 are increased on T cells in the sMLN compared with the cMLN. DCs from the cMLN and colon are unable to metabolize vitamin A to retinoic acid (RA); thus, DCs may contribute to the differential expression of tissue homing markers observed in the sMLN and cMLN. In summary, the sMLN and cMLN, and the DCs that migrate to these LNs are anatomically and immunologically separate. This segregation allows immune responses in the SI and colon to be controlled independently.

摘要

小肠(SI)和结肠中的树突状细胞(DC)是直接引导肠道免疫反应的基础;它们迁移至肠系膜淋巴结(MLN)并激活T细胞。我们证明了来自肠道的淋巴引流存在解剖学上的分隔,具体而言,来自SI和结肠的DC迁移至MLN内不同的淋巴结,此处分别称为sMLN和cMLN。因此,在SI和结肠中观察到的不同频率的DC亚群反映在sMLN和cMLN中的DC之间。与SI吸收食物的功能一致,喂食抗原呈递于sMLN而非cMLN。此外,与cMLN相比,sMLN中T细胞上CCR9和α4β7的表达水平升高。来自cMLN和结肠的DC无法将维生素A代谢为视黄酸(RA);因此,DC可能导致了在sMLN和cMLN中观察到的组织归巢标志物的差异表达。总之,sMLN和cMLN以及迁移至这些淋巴结的DC在解剖学和免疫学上是分离的。这种分隔使得SI和结肠中的免疫反应能够独立控制。

相似文献

1
The lymph nodes draining the small intestine and colon are anatomically separate and immunologically distinct.引流小肠和结肠的淋巴结在解剖学上是分开的,在免疫学上也是不同的。
Mucosal Immunol. 2016 Mar;9(2):468-78. doi: 10.1038/mi.2015.77. Epub 2015 Sep 2.
2
Monitoring and Modulation of Inducible Foxp3 Regulatory T-Cell Differentiation in the Lymph Nodes Draining the Small Intestine and Colon.监测和调节小肠和结肠引流淋巴结中诱导性Foxp3调节性T细胞的分化
Methods Mol Biol. 2017;1559:241-254. doi: 10.1007/978-1-4939-6786-5_16.
3
Differential T cell homing to colon vs. small intestine is imprinted by local CD11c APCs that determine homing receptors.T细胞向结肠与小肠的差异性归巢由决定归巢受体的局部CD11c抗原呈递细胞所印记。
J Leukoc Biol. 2017 Dec;102(6):1381-1388. doi: 10.1189/jlb.1A1116-463RR. Epub 2017 Sep 26.
4
Small intestinal CD103+ dendritic cells display unique functional properties that are conserved between mice and humans.小肠CD103⁺树突状细胞表现出在小鼠和人类之间保守的独特功能特性。
J Exp Med. 2008 Sep 1;205(9):2139-49. doi: 10.1084/jem.20080414. Epub 2008 Aug 18.
5
Colonic tolerance develops in the iliac lymph nodes and can be established independent of CD103(+) dendritic cells.结肠耐受性在髂淋巴结中形成,并且可以独立于CD103(+)树突状细胞而建立。
Mucosal Immunol. 2016 Jul;9(4):894-906. doi: 10.1038/mi.2015.118. Epub 2015 Nov 18.
6
Gut homing receptors on CD8 T cells are retinoic acid dependent and not maintained by liver dendritic or stellate cells.CD8 T细胞上的肠道归巢受体依赖视黄酸,并非由肝脏树突状细胞或星状细胞维持。
Gastroenterology. 2009 Jul;137(1):320-9. doi: 10.1053/j.gastro.2009.02.046. Epub 2009 Feb 21.
7
Bile retinoids imprint intestinal CD103+ dendritic cells with the ability to generate gut-tropic T cells.胆酸盐视黄醇可在肠道中 CD103+树突状细胞上留下印迹,使其具有产生肠道归巢 T 细胞的能力。
Mucosal Immunol. 2011 Jul;4(4):438-47. doi: 10.1038/mi.2010.91. Epub 2011 Feb 2.
8
CCR7 is critically important for migration of dendritic cells in intestinal lamina propria to mesenteric lymph nodes.CCR7对于树突状细胞从肠固有层迁移至肠系膜淋巴结至关重要。
J Immunol. 2006 Jan 15;176(2):803-10. doi: 10.4049/jimmunol.176.2.803.
9
Activation of Plasmacytoid Dendritic Cells in Colon-Draining Lymph Nodes during Citrobacter rodentium Infection Involves Pathogen-Sensing and Inflammatory Pathways Distinct from Conventional Dendritic Cells.鼠柠檬酸杆菌感染期间结肠引流淋巴结中浆细胞样树突状细胞的激活涉及不同于传统树突状细胞的病原体感知和炎症途径。
J Immunol. 2016 Jun 1;196(11):4750-9. doi: 10.4049/jimmunol.1600235. Epub 2016 Apr 27.
10
Stromal mesenteric lymph node cells are essential for the generation of gut-homing T cells in vivo.肠系膜基质淋巴结细胞对于体内归巢至肠道的T细胞的产生至关重要。
J Exp Med. 2008 Oct 27;205(11):2483-90. doi: 10.1084/jem.20080039. Epub 2008 Oct 13.

引用本文的文献

1
Progressive changes in phenotype, transcriptome and proliferation capacity characterise continued maturation and migration of intestinal cDCs in homeostasis.表型、转录组和增殖能力的渐进性变化是肠道cDC在稳态中持续成熟和迁移的特征。
Nat Commun. 2025 Sep 2;16(1):8204. doi: 10.1038/s41467-025-63559-z.
2
Microbiota modulate immune cell populations and drive dynamic structural changes in gut-associated lymphoid tissue.微生物群调节免疫细胞群体,并驱动肠道相关淋巴组织的动态结构变化。
Gut Microbes. 2025 Dec;17(1):2543908. doi: 10.1080/19490976.2025.2543908. Epub 2025 Aug 13.
3
Mechanisms conferring multi-layered protection against intestinal Salmonella Typhimurium infection.

本文引用的文献

1
Role and species-specific expression of colon T cell homing receptor GPR15 in colitis.结肠T细胞归巢受体GPR15在结肠炎中的作用及物种特异性表达
Nat Immunol. 2015 Feb;16(2):207-213. doi: 10.1038/ni.3079. Epub 2014 Dec 22.
2
Heterogeneity across the murine small and large intestine.小鼠小肠和大肠之间的异质性。
World J Gastroenterol. 2014 Nov 7;20(41):15216-32. doi: 10.3748/wjg.v20.i41.15216.
3
Signal regulatory protein alpha (SIRPα) regulates the homeostasis of CD103(+) CD11b(+) DCs in the intestinal lamina propria.信号调节蛋白α(SIRPα)调节肠固有层中CD103(+) CD11b(+) 树突状细胞的稳态。
赋予对肠道鼠伤寒沙门氏菌感染多层保护的机制。
FEMS Microbiol Rev. 2025 Jan 14;49. doi: 10.1093/femsre/fuaf038.
4
A hierarchy of intestinal antigens instructs the CD4 T cell receptor repertoire.肠道抗原的层级结构指导CD4 T细胞受体库。
Immunity. 2025 May 13;58(5):1217-1235.e4. doi: 10.1016/j.immuni.2025.04.011. Epub 2025 May 2.
5
MS275 induces tumor immunosuppression by upregulating PD-L1 and enhances the efficacy of anti-PD-1 immunotherapy in colorectal cancer.MS275通过上调程序性死亡受体配体1(PD-L1)诱导肿瘤免疫抑制,并增强抗程序性死亡蛋白1(PD-1)免疫疗法在结直肠癌中的疗效。
Cancer Immunol Immunother. 2025 Mar 17;74(5):150. doi: 10.1007/s00262-025-04004-4.
6
Liver-draining portal lymph node responds to enteric nematode infection by generating highly parasite-specific follicular T helper and B cell responses.引流肝脏的门静脉淋巴结通过产生高度寄生虫特异性的滤泡辅助性T细胞和B细胞反应来应对肠道线虫感染。
Front Immunol. 2025 Feb 28;16:1483274. doi: 10.3389/fimmu.2025.1483274. eCollection 2025.
7
use multiple mechanisms to disseminate from the intestinal lamina propria to the mesenteric lymph nodes.利用多种机制从肠固有层扩散至肠系膜淋巴结。
Microbiol Spectr. 2025 Feb 4;13(2):e0259524. doi: 10.1128/spectrum.02595-24. Epub 2024 Dec 23.
8
Transport functions of intestinal lymphatic vessels.肠道淋巴管的运输功能。
Nat Rev Gastroenterol Hepatol. 2025 Feb;22(2):127-145. doi: 10.1038/s41575-024-00996-z. Epub 2024 Nov 4.
9
Fecal microbiota transplantation alleviates food allergy in neonatal mice via the PD-1/PD-L1 pathway and change of the microbiota composition.粪便微生物群移植通过PD-1/PD-L1途径和微生物群组成的改变减轻新生小鼠的食物过敏。
World Allergy Organ J. 2024 Oct 1;17(10):100969. doi: 10.1016/j.waojou.2024.100969. eCollection 2024 Oct.
10
The renaissance of oral tolerance: merging tradition and new insights.口服耐受的复兴:融合传统与新见解
Nat Rev Immunol. 2025 Jan;25(1):42-56. doi: 10.1038/s41577-024-01077-7. Epub 2024 Sep 6.
Eur J Immunol. 2014 Dec;44(12):3658-68. doi: 10.1002/eji.201444859. Epub 2014 Oct 27.
4
Regional specialization within the intestinal immune system.肠道免疫系统的区域专业化。
Nat Rev Immunol. 2014 Oct;14(10):667-85. doi: 10.1038/nri3738. Epub 2014 Sep 19.
5
CCR2(+)CD103(-) intestinal dendritic cells develop from DC-committed precursors and induce interleukin-17 production by T cells.CCR2(+)CD103(-)肠道树突状细胞由DC定向前体发育而来,并诱导T细胞产生白细胞介素-17。
Mucosal Immunol. 2015 Mar;8(2):327-39. doi: 10.1038/mi.2014.70. Epub 2014 Aug 20.
6
The alarmin IL-33 promotes regulatory T-cell function in the intestine.警报素 IL-33 可促进肠道中调节性 T 细胞的功能。
Nature. 2014 Sep 25;513(7519):564-568. doi: 10.1038/nature13577. Epub 2014 Jul 16.
7
Lymph-borne CD8α+ dendritic cells are uniquely able to cross-prime CD8+ T cells with antigen acquired from intestinal epithelial cells.经淋巴转运的CD8α⁺树突状细胞具有独特的能力,能够利用从肠道上皮细胞获取的抗原交叉启动CD8⁺T细胞。
Mucosal Immunol. 2015 Jan;8(1):38-48. doi: 10.1038/mi.2014.40. Epub 2014 May 21.
8
Role of the microbiota in immunity and inflammation.微生物群在免疫和炎症中的作用。
Cell. 2014 Mar 27;157(1):121-41. doi: 10.1016/j.cell.2014.03.011.
9
CXCR4 promotes B cell egress from Peyer's patches.CXCR4 促进 B 细胞从派伊尔斑中迁出。
J Exp Med. 2013 Jun 3;210(6):1099-107. doi: 10.1084/jem.20122574. Epub 2013 May 13.
10
IRF4 transcription-factor-dependent CD103(+)CD11b(+) dendritic cells drive mucosal T helper 17 cell differentiation.IRF4 转录因子依赖性 CD103(+)CD11b(+)树突状细胞驱动黏膜 T 辅助 17 细胞分化。
Immunity. 2013 May 23;38(5):958-69. doi: 10.1016/j.immuni.2013.03.009. Epub 2013 May 9.