一种细菌效应蛋白促进了Stat3的核转移,从而诱导IL-10的产生
Laura Berneking1, Indra Bekere1, Sören Rob1
1Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
European journal of cell biology
|October 8, 2023
概括
耶尔西尼亚效应剂YopM通过增加互白素-10 (IL-10) 来抑制宿主免疫力. YopM通过将Stat3蛋白移动到细胞核中,独立于RSK1激活来促进IL-10的产生.
科学领域:
- 免疫学 免疫学 免疫学
- 微生物学 微生物学
- 分子生物学分子生物学
背景情况:
- 耶尔西尼亚效应剂YopM抑制宿主免疫力,并促进抗炎性互白素-10 (IL-10) 的产生.
- 以前已经证明YopM可以通过RSK1激酶激活在人类巨细胞中诱导IL-10基因表达.
研究的目的:
- 研究YopM抑制宿主免疫反应的分子机制.
- 阐明JAK-STAT信号通路在YopM介导的IL-10诱导中的作用.
主要方法:
- 转录组分析以确定受影响的基因表达途径.
- 巨细胞感染的模型与Yersinia enterocolitica.
- 西方涂抹和基因淘汰技术用于分析蛋白质转位和基因表达.
主要成果:
- YopM显著影响JAK-STAT信号通路中的基因.
- 在受感染的巨细胞中,YopM促进了转录因子Stat3的核转位.
- 斯塔特3倒置抑制了YopM诱导的IL-10基因表达.
- 由YopM诱导的Stat3核转位独立于IL-10,RSK1激活和Stat3氨酸酸化.
结论:
- YopM利用Stat3核转位作为一种增加IL-10基因表达的机制.
- 这种Stat3介导的途径与RSK1激活一起代表了一个额外的机制,YopM通过这种机制抑制宿主免疫力.
更多相关视频
相关概念视频
The JAK-STAT Signaling Pathway
8.9K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
8.9K
NF-κB-dependent Signaling Pathway
7.5K
The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
NF-κB-dependent Signaling Mechanism
The...
7.5K
Regulation of Nuclear Protein Sorting
2.4K
Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
2.4K
TGF - β Signaling Pathway
7.4K
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
7.4K
T Cell Types and Functions
1.0K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
1.0K
Co-activators and Co-repressors
7.4K
Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
7.4K


