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

YAP 通过调节 M1/M2 巨噬细胞极化和肠道微生物稳态加重炎症性肠病。

YAP Aggravates Inflammatory Bowel Disease by Regulating M1/M2 Macrophage Polarization and Gut Microbial Homeostasis.

机构信息

State Key Laboratory of Cell Biology, Key Laboratory of Systems Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Innovation Center for Cell Signaling Network, Shanghai 200031, China.

College of Life Sciences, Shanghai University, Shanghai 200444, China.

出版信息

Cell Rep. 2019 Apr 23;27(4):1176-1189.e5. doi: 10.1016/j.celrep.2019.03.028.


DOI:10.1016/j.celrep.2019.03.028
PMID:31018132
Abstract

Inflammation, epithelial cell regeneration, macrophage polarization, and gut microbial homeostasis are critical for the pathological processes associated with inflammatory bowel disease (IBD). YAP (Yes-associated protein) is a key component of the Hippo pathway and was recently suggested to promote epithelial cell regeneration for IBD recovery. However, it is unclear how YAP regulates macrophage polarization, inflammation, and gut microbial homeostasis. Although YAP has been shown to promote epithelial regeneration and alleviate IBD, here we show that YAP in macrophages aggravates IBD, accompanied by the production of antimicrobial peptides and changes in gut microbiota. YAP impairs interleukin-4 (IL-4)/IL-13-induced M2 macrophage polarization while promoting lipopolysaccharide (LPS)/interferon γ (IFN-γ)-triggered M1 macrophage activation for IL-6 production. In addition, YAP expression is differently regulated during the induction of M2 versus M1 macrophages. This study suggests that fully understanding the multiple functions of YAP in different cell types is crucial for IBD therapy.

摘要

炎症、上皮细胞再生、巨噬细胞极化和肠道微生物稳态对于与炎症性肠病(IBD)相关的病理过程至关重要。YAP(Yes 相关蛋白)是 Hippo 通路的关键组成部分,最近被认为可促进上皮细胞再生,从而促进 IBD 恢复。然而,YAP 如何调节巨噬细胞极化、炎症和肠道微生物稳态尚不清楚。尽管已经表明 YAP 可促进上皮细胞再生并减轻 IBD,但在这里我们表明巨噬细胞中的 YAP 会加重 IBD,同时还伴随着抗菌肽的产生和肠道微生物群的变化。YAP 会损害白细胞介素 4(IL-4)/白细胞介素 13(IL-13)诱导的 M2 巨噬细胞极化,同时促进脂多糖(LPS)/干扰素 γ(IFN-γ)触发的 M1 巨噬细胞活化以产生白细胞介素 6(IL-6)。此外,YAP 的表达在诱导 M2 型与 M1 型巨噬细胞的过程中受到不同的调控。本研究表明,充分了解 YAP 在不同细胞类型中的多种功能对于 IBD 治疗至关重要。

相似文献

[1]
YAP Aggravates Inflammatory Bowel Disease by Regulating M1/M2 Macrophage Polarization and Gut Microbial Homeostasis.

Cell Rep. 2019-4-23

[2]
Ninjurin1 deficiency aggravates colitis development by promoting M1 macrophage polarization and inducing microbial imbalance.

FASEB J. 2020-6

[3]
The pentacyclic triterpene Lupeol switches M1 macrophages to M2 and ameliorates experimental inflammatory bowel disease.

Int Immunopharmacol. 2016-1

[4]
Selenoprotein S maintains intestinal homeostasis in ulcerative colitis by inhibiting necroptosis of colonic epithelial cells through modulation of macrophage polarization.

Theranostics. 2024

[5]
Excretory/Secretory Products From Adult Worms Attenuated DSS-Induced Colitis in Mice by Driving PD-1-Mediated M2 Macrophage Polarization.

Front Immunol. 2020

[6]
Heme protects intestinal mucosal barrier in DSS-induced colitis through regulating macrophage polarization in both HO-1-dependent and HO-1-independent way.

FASEB J. 2020-6

[7]
Atox1 regulates macrophage polarization in intestinal inflammation via ROS-NLRP3 inflammasome pathway.

J Transl Med. 2024-5-25

[8]
Ginsenoside Rg1 ameliorated experimental colitis by regulating the balance of M1/M2 macrophage polarization and the homeostasis of intestinal flora.

Eur J Pharmacol. 2022-2-15

[9]
Hippo Signaling Controls NLR Family Pyrin Domain Containing 3 Activation and Governs Immunoregulation of Mesenchymal Stem Cells in Mouse Liver Injury.

Hepatology. 2019-6-21

[10]
Depression Exacerbates Dextran Sulfate Sodium-Induced Colitis via IRF5-Mediated Macrophage Polarization.

Dig Dis Sci. 2023-4

引用本文的文献

[1]
Network pharmacology to explore the novel anti-inflammatory mechanism of naringenin in intestinal ischemia/reperfusion injury.

Front Immunol. 2025-8-8

[2]
KLF11 alleviates rheumatoid arthritis by regulating M1 macrophage polarization via downregulation of YAP1 expression.

Arthritis Res Ther. 2025-8-26

[3]
FGF15/FGFR4 signaling suppresses M1 macrophage polarization and multi-organ inflammation in septic mice by inhibiting H3K18 lactylation-driven Irf7 expression through NF2-Hippo activation.

Cell Death Dis. 2025-8-19

[4]
MicroRNA: role in macrophage polarisation and colorectal cancer pathogenesis.

Front Cell Dev Biol. 2025-7-23

[5]
Hyperandrogenism-mediated YAP activation drives ovarian inflammation and pyroptosis in PCOS: implications for follicular dysfunction.

J Ovarian Res. 2025-7-30

[6]
The role of macrophages in renal fibrosis and therapeutic prospects.

PeerJ. 2025-7-23

[7]
Cardiomyocyte YAP represses myocardial inflammation and fibrosis and restrains MEF2 regulated gene expression.

Am J Physiol Heart Circ Physiol. 2025-7-10

[8]
[Ecliptasaponin A ameliorates DSS-induced colitis in mice by suppressing M1 macrophage polarization inhibiting the JAK2/STAT3 pathway].

Nan Fang Yi Ke Da Xue Xue Bao. 2025-6-20

[9]
Exercise-induced Metabolite N-lactoyl-phenylalanine Ameliorates Colitis by Inhibiting M1 Macrophage Polarization Via the Suppression of the NF-κB Signaling Pathway.

Cell Mol Gastroenterol Hepatol. 2025-6-23

[10]
Fungi and cancer: unveiling the complex role of fungal infections in tumor biology and therapeutic resistance.

Front Cell Infect Microbiol. 2025-6-10

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