文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

微皱褶(M)细胞:肠道上皮中的重要免疫监视哨点。

Microfold (M) cells: important immunosurveillance posts in the intestinal epithelium.

机构信息

The Roslin Institute and Royal-Dick School of Veterinary Sciences, University of Edinburgh, Easter Bush, Midlothian, Scotland, UK.

出版信息

Mucosal Immunol. 2013 Jul;6(4):666-77. doi: 10.1038/mi.2013.30. Epub 2013 May 22.


DOI:10.1038/mi.2013.30
PMID:23695511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3686595/
Abstract

The transcytosis of antigens across the gut epithelium by microfold cells (M cells) is important for the induction of efficient immune responses to some mucosal antigens in Peyer's patches. Recently, substantial progress has been made in our understanding of the factors that influence the development and function of M cells. This review highlights these important advances, with particular emphasis on: the host genes which control the functional maturation of M cells; how this knowledge has led to the rapid advance in our understanding of M-cell biology in the steady state and during aging; molecules expressed on M cells which appear to be used as "immunosurveillance" receptors to sample pathogenic microorganisms in the gut; how certain pathogens appear to exploit M cells to infect the host; and finally how this knowledge has been used to specifically target antigens to M cells to attempt to improve the efficacy of mucosal vaccines.

摘要

微皱褶细胞(M 细胞)将抗原穿过肠上皮细胞的转胞吞作用对于诱导派尔集合淋巴结中某些黏膜抗原的有效免疫反应非常重要。最近,人们对影响 M 细胞发育和功能的因素有了更深入的了解。本综述强调了这些重要的进展,特别强调了:控制 M 细胞功能成熟的宿主基因;这些知识如何使我们对稳态和衰老过程中 M 细胞生物学的理解迅速发展;M 细胞上表达的似乎被用作“免疫监视”受体来检测肠道中病原体的分子;某些病原体如何利用 M 细胞感染宿主;最后,如何利用这些知识将抗原特异性靶向 M 细胞,以试图提高黏膜疫苗的效果。

相似文献

[1]
Microfold (M) cells: important immunosurveillance posts in the intestinal epithelium.

Mucosal Immunol. 2013-5-22

[2]
Polycomb Repressive Complex 2 Regulates Genes Necessary for Intestinal Microfold Cell (M Cell) Development.

Cell Mol Gastroenterol Hepatol. 2021

[3]
Development of Functional Microfold (M) Cells from Intestinal Stem Cells in Primary Human Enteroids.

PLoS One. 2016-1-28

[4]
Peyer's patch M cells derived from Lgr5(+) stem cells require SpiB and are induced by RankL in cultured "miniguts".

Mol Cell Biol. 2012-7-9

[5]
Retinoic Acid and Lymphotoxin Signaling Promote Differentiation of Human Intestinal M Cells.

Gastroenterology. 2020-7

[6]
Lymphoepithelial interactions trigger specific regulation of gene expression in the M cell-containing follicle-associated epithelium of Peyer's patches.

J Immunol. 2002-4-15

[7]
RANKL is necessary and sufficient to initiate development of antigen-sampling M cells in the intestinal epithelium.

J Immunol. 2009-11-1

[8]
Particle uptake by Peyer's patches: a pathway for drug and vaccine delivery.

Expert Opin Drug Deliv. 2004-11

[9]
Keynote review: intestinal Peyer's patch M cells and oral vaccine targeting.

Drug Discov Today. 2005-9-1

[10]
Transcription factor Spi-B-dependent and -independent pathways for the development of Peyer's patch M cells.

Mucosal Immunol. 2012-12-5

引用本文的文献

[1]
The putative AraC-type transcriptional regulator STM1082 facilitates pathogenicity through modulation of intestinal invasion and intracellular replication.

Virulence. 2025-12

[2]
Zeolite for preventing periparturient hypocalcemia in dairy cows: mechanisms and application strategies.

Front Vet Sci. 2025-8-8

[3]
Intestinal organoid models as tools to interrogate the physiology of human mucosal tissues and host-microbe interactions.

mSphere. 2025-8-26

[4]
Pyruvate-GPR31 axis induces LysoDC dendrite protrusion to M-cell pockets for effective immune responses.

Gut Microbes. 2025-12

[5]
Gut expression of CD71 and co-localisation with Dec-1 associated with high levels of serum SIgA and disease activity in SpA.

Sci Rep. 2025-6-4

[6]
Oral Supplementation with Modified Natural Clinoptilolite Protects Against Cadmium Toxicity in ICR (CD-1) Mice.

Toxics. 2025-4-27

[7]
Bat organoids reveal antiviral responses at epithelial surfaces.

Nat Immunol. 2025-5-21

[8]
Latest Advanced Techniques for Improving Intestinal Organoids Limitations.

Stem Cell Rev Rep. 2025-5-19

[9]
Antigen Uptake in the Gut: An Underappreciated Piece to the Puzzle?

Annu Rev Immunol. 2025-4

[10]
Mechanobiological Approach for Intestinal Mucosal Immunology.

Biology (Basel). 2025-1-22

本文引用的文献

[1]
Can DCs be distinguished from macrophages by molecular signatures?

Nat Immunol. 2013-3

[2]
Luminal bacteria recruit CD103+ dendritic cells into the intestinal epithelium to sample bacterial antigens for presentation.

Immunity. 2013-2-7

[3]
The functional maturation of M cells is dramatically reduced in the Peyer's patches of aged mice.

Mucosal Immunol. 2013-1-30

[4]
Transcription factor Spi-B-dependent and -independent pathways for the development of Peyer's patch M cells.

Mucosal Immunol. 2012-12-5

[5]
Salmonella transforms follicle-associated epithelial cells into M cells to promote intestinal invasion.

Cell Host Microbe. 2012-11-15

[6]
Mycobacterium avium subsp. paratuberculosis invades through M cells and enterocytes across ileal and jejunal mucosa of lambs.

Res Vet Sci. 2012-10-31

[7]
Spi-B is critical for plasmacytoid dendritic cell function and development.

Blood. 2012-10-11

[8]
Identification of novel genes selectively expressed in the follicle-associated epithelium from the meta-analysis of transcriptomics data from multiple mouse cell and tissue populations.

DNA Res. 2012-9-18

[9]
Peyer's patch M cells derived from Lgr5(+) stem cells require SpiB and are induced by RankL in cultured "miniguts".

Mol Cell Biol. 2012-7-9

[10]
Cutting Edge: Brucella abortus exploits a cellular prion protein on intestinal M cells as an invasive receptor.

J Immunol. 2012-7-6

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

推荐工具

医学文档翻译智能文献检索