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Identification of novel Helicobacter pylori adhesins and host cell receptors facilitating bacterial access to beta1 integrin and translocation of CagA

Identification of novel Helicobacter pylori adhesins and host cell receptors facilitating bacterial access to beta1 integrin and translocation of CagA
新型幽门螺杆菌粘附素和宿主细胞受体的鉴定促进细菌接触β1整合素和CagA易位
批准号:
195217982
负责人:
Professor Dr. Rainer Haas
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2011
资助国家:
德国
项目状态:
已结题
起止时间:
2010-12-31 至 2020-12-31

项目摘要

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中文摘要
翻译
幽门螺杆菌感染人的胃粘膜,引起慢性胃炎、溃疡,最终导致胃癌。病原菌株利用β 1整合素和癌胚抗原相关细胞粘附分子(CEACAMs)作为宿主细胞受体,将细菌癌蛋白细胞毒素相关抗原A (CagA)注入宿主细胞。胃上皮形成紧密的上皮细胞层,由连接复合物(间隙连接、紧密连接、粘附连接、桥粒、ceacam等)严格连接。ceacam通常位于胃上皮的连接处和顶端,而β 1整合素位于胃基底外侧。在本项目中,我们希望研究幽门螺杆菌在类体内条件下与这些受体,特别是β 1整合素接触的策略和机制,以便能够将其癌蛋白CagA注射到这些细胞中。因此,我们寻找新的细菌粘附素和宿主细胞受体,并试图在分子水平上理解幽门螺杆菌粘附素- ceacam相互作用,以更好地理解所涉及的信号事件。此外,我们开发了复杂的新型细胞培养模型,以紧密的单层生长来研究这些问题。最后,我们计划在适当的动物模型中应用亲和成熟的CEACAM免疫球蛋白样变量(IgV)结构域来干扰CagA在体外和体内的易位。
英文摘要
The bacterial pathogen Helicobacter pylori infects the human stomach mucosa, causing chronic gastritis, ulceration and eventually gastric cancer. Pathogenic strains inject the bacterial oncoprotein Cytotoxin-associated antigen A (CagA) into host cells by exploiting beta1 Integrin and carcinoembryonic antigen-related cell adhesion molecules (CEACAMs) as host cell receptors. The gastric epithelium forms a tight layer of epithelial cells strictly connected by junctional complexes (gap junctions, tight junctions, adherence junctions, desmosomes, CEACAMs, etc.). Whereas CEACAMs are usually located at the junctions and on the apical side of the gastric epithelium, beta1 integrins are located at the basolateral side. In this project we want to study the strategies and mechanisms used by H. pylori to make contact to these receptors, especially to the beta1 integrins, under in vivo-like conditions, in order to be able to inject its oncoprotein CagA into these cells. We therefore search for novel bacterial adhesins and host cell receptors and we try to understand the H. pylori adhesin-CEACAM interaction at the molecular level to better understand the signaling events involved. Furthermore, we developed sophisticated novel cell culture models growing as tight monolayers to study these questions. Finally we plan to apply affinity-maturated CEACAM Immunglobulin-like variable (IgV) domains to interfere with CagA translocation in vitro and in vivo in appropriate animal models.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1111/mmi.14772
发表时间: 2021-06-28
期刊: MOLECULAR MICROBIOLOGY
影响因子: 3.6
作者: [Lettl, Clara, Haas, Rainer, Fischer, Wolfgang]
通讯作者: Fischer, Wolfgang
DOI: 10.1128/mbio.03256-19
发表时间: 2020-01-01
期刊: MBIO
影响因子: 6.4
作者: [Behrens, Ina-Kristin, Busch, Benjamin, Haas, Rainer]
通讯作者: Haas, Rainer
DOI: 10.15252/embj.201798664
发表时间: 2018-07-02
期刊: EMBO JOURNAL
影响因子: 11.4
作者: [Bonsor, Daniel A., Zhao, Qing, Sundberg, Eric J.]
通讯作者: Sundberg, Eric J.
Analysis of Helicobacter pylori infections in Africa, bacterial virulence factors but lack of pathology
Molecular basis of alpha5/beta1 integrin exploitation by the Helicobacter pylori type IV secretion system
Correlation of Helicobacter pylori infection with gastroduodenal diseases in Nigeria - improvement of diagnosis and treatment
Helicobacter pylori cag-Type IV Secretion System: Integrin interaction and mechanism of CagA protein translocation
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