The biology of the beige-like protein LRBA in health and disease
The biology of the beige-like protein LRBA in health and disease
批准号:
267792999
负责人:
Professor Dr. Bodo Grimbacher
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2015
资助国家:
德国
项目状态:
已结题
起止时间:
2014-12-31 至 2017-12-31
中文摘要
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英文摘要
We discovered in 2012 that mutations in the gene LRBA in humans lead to an immune dysregulation syndrome (López-Herrera et al., AJHG). This disease is characterized by a chronic inflammatory bowel disease, severe autoimmunity and an increased infection susceptibility. Not much is know on the biological functions of LRBA:-LRBA is expressed ubiquitously (Wu C et al., 2009)-Its expression increases following cell activation (Wang X et al., 2000)-From co-localization studies with fluorescence microscopy we know that LRBA is located at endosomes and lysosomes (Wang JW et al., 2001)-Proteins from the same family (BEACH proteins) mediate the link between cellular vesicles and the actin cytoskeleton (Cullinane et al., 2013)-A link between BEACH proteins and autophagy is published (Rahman et al., 2012) In this project we suggest to further study the genetics and the biology of LRBA to learn about its role in the immune system and to identify possible novel targets for the treatment of inflammatory bowel disease, severe autoimmunity and infection susceptibility.In WP1 we will approach the question why the lack of an ubiquitously expressed protein leads to a phenotype limited to the immune system. We will study the expression and splice variants of LRBA and its homologs in different cell populations and following various stimuli. Moreover, we will study the gene expression profile of LRBA-deficient cells. Our preliminary data show that LRBA (320 kDa in size) forms complexes of 880 kDa. In WP2 we wish to identify interaction partners of LRBA. We propose to do this by two means: The hypothesis-driven approach, by identifying potential interaction partners by co-immunoprecipitation; and the hypothesis-free approach, by SILAC-mass spectroscopy. We will study the function of LRBA in WP3 by verifying or falsifying the following hypotheses:-LRBA is important for the chemotaxis of lymphocytes-LRBA plays a critical role in immune receptor recycling-LRBA plays a critical role in autophagy-LRBA interferes with the mTOR signaling pathwayDiscoveries on the function of genes/proteins of the human immune system, which manifest as monogenetic human disease traits, are especially interesting for translational research, as these genes/proteins define Achilles heels of the immune system, specifically relevant for therapeutic targeting.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1038/icb.2017.52
发表时间:
2017-10-01
期刊:
IMMUNOLOGY AND CELL BIOLOGY
影响因子:
4
作者:
[Gamez-Diaz, Laura, Neumann, Julika, Jung, Sophie]
通讯作者:
Jung, Sophie
Unraveling the molecular pathophysiological landscape in primary immunodeficiencies to improve personalized medicine approaches.
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批准号:458854985
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项目类别:Research Grants
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资助金额:$0.0万
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财政年份:2021
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负责人:Professor Dr. Bodo Grimbacher
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依托单位:
Integrative Multi-Omics Analysis of Primary Antibody Deficiency (PAD) Patients for Stratification Accordingto Cellular Pathways
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批准号:423367839
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项目类别:Research Grants
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资助金额:$0.0万
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财政年份:2019
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负责人:Professor Dr. Bodo Grimbacher
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依托单位:
Genetik der kongenitalen Neutropenie
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批准号:5441188
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项目类别:Clinical Research Units
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资助金额:$0.0万
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财政年份:2004
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负责人:Professor Dr. Bodo Grimbacher
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依托单位:
Der molekulargenetische Defekt des Hyper-IgE-Syndroms
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批准号:5367629
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项目类别:Independent Junior Research Groups
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资助金额:$0.0万
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财政年份:2002
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负责人:Professor Dr. Bodo Grimbacher
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依托单位:
Clinic and molekular defect in the hyper-IgE-Syndrome
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批准号:5239908
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项目类别:Research Grants
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资助金额:$0.0万
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财政年份:2000
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负责人:Professor Dr. Bodo Grimbacher
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依托单位:
Function and impact of the transcription factor ZNF341 in lymphocytes
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批准号:519635399
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项目类别:Research Grants
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资助金额:$0.0万
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财政年份:--
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负责人:Professor Dr. Bodo Grimbacher
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依托单位:
国内基金
海外基金
PPARγ T166磷酸化调控ADSC-beige细胞定向分化的机制及其干预
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批准号:LQ23H070001
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项目类别:省市级项目
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资助金额:--
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批准年份:2023
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负责人:杨南飞
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依托单位:
Cbx4在棕色脂肪能量代谢以及Beige细胞形成中的作用
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批准号:31570783
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项目类别:面上项目
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资助金额:62.0万元
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批准年份:2015
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负责人:潘东宁
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依托单位:
二仙汤对更年期小鼠Beige细胞产热功能的影响及其机制研究
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批准号:81403203
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项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2014
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负责人:李润美
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依托单位: