Arrestins in TLR4 Signaling in Macrophages
Arrestins in TLR4 Signaling in Macrophages
批准号:
8513771
负责人:
Narayanan Parameswaran
金额:
$26.76万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-03 至 2015-07-31
关键词:
AffectArrestinsArthritisBiochemicalCytokine GeneDataDevelopmentDiseaseDrug TargetingFamilyFunctional disorderG-Protein-Coupled ReceptorsGene ExpressionGram-Negative BacteriaHealthInfiltrationInflammationInflammation MediatorsInflammatoryInflammatory ResponseLigandsLipopolysaccharidesMaintenanceMediatingMicrobeMolecularMusPathogenesisPatternPharmaceutical PreparationsPlayProcessProductionProteinsPublishingReceptor SignalingRegulationRheumatoid ArthritisRoleScaffolding ProteinSignal PathwaySignal TransductionTLR4 geneTestingTherapeuticToll-like receptorscombatcytokinedesensitizationhuman diseasein vivoinsightmacrophagemembernon-visual arrestinsnovelpathogenprotein protein interactionresearch studytoll-like receptor 4
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Production of proinflammatory cytokines by macrophages significantly contributes to the pathogenesis of many inflammatory diseases including arthritis. Therefore, understanding the signaling mechanisms involved in the regulation of expression of pro-inflammatory molecules by macrophages is pivotal to developing drugs to combat inflammatory diseases. Recent studies have implicated Toll-like receptors (TLRs) in the initiation and maintenance of inflammation in a number of human diseases. Of particular importance is the role of TLR4, which critically regulates cytokine production and is therefore a drug target in inflammatory diseases. Hence, understanding the biochemical mechanisms by which TLR4-stimulated signaling pathways affect expression of inflammatory molecules is highly significant. Recent studies have demonstrated a critical role for non-visual arrestins (ARR2 and ARR3) in the regulation of TLR signaling and pathophysiology. Arrestins (ARRs) are scaffolding proteins originally discovered for their role in G- protein coupled receptor (GPCR) desensitization. Evidence indicates that ARR2 and 3 interact with distinct proteins and consequently regulate TLR4 signaling and inflammatory gene expression in macrophages and in vivo in mice. The objective of this application is to understand the biochemical mechanisms by which ARR2 and ARR3 regulate TLR4 signaling in macrophages and to test how this relates to inflammation in mice. To accomplish this objective, we will test the following hypotheses: (a) ARR2 and 3 play a crucial role in TLR4 signaling, and inflammatory mediator production in macrophages, and (b), this occurs via distinct protein-protein interactions, and (c) ARR2 and 3 are critically involved in TLR4-mediated inflammatory response in mice in vivo. Our studies should provide important insight into the mechanisms of TLR4 signaling in macrophages as well as provide potential therapeutic strategies for targeting TLR4 signaling in a variety of inflammatory diseases. PUBLIC HEALTH RELEVANCE: Toll-like receptor-4 activation in macrophages plays an important role in the development of various inflammatory diseases. Major objective of this application is to understand the regulation of TLR4-stimulated signaling pathways in macrophages and test as to how it relates to inflammatory diseases.
期刊论文(9)
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DOI:
10.1152/physiolgenomics.00066.2017
发表时间:
2017-11
期刊:
Physiological genomics
影响因子:
4.6
作者:
[Taehyung Lee;N. Packiriswamy;E. Lee;P. C. Lucas;L. McCabe;N. Parameswaran]
通讯作者:
Taehyung Lee;N. Packiriswamy;E. Lee;P. C. Lucas;L. McCabe;N. Parameswaran
DOI:
10.1002/jcp.25216
发表时间:
2016-05
期刊:
Journal of cellular physiology
影响因子:
5.6
作者:
[Lee T, Lee E, Arrollo D, Lucas PC, Parameswaran N]
通讯作者:
Parameswaran N
DOI:
10.1002/jcp.24636
发表时间:
2014-11
期刊:
JOURNAL OF CELLULAR PHYSIOLOGY
影响因子:
5.6
作者:
[Britton, Robert A., Irwin, Regina, Quach, Darin, Schaefer, Laura, Zhang, Jing, Lee, Taehyung, Parameswaran, Narayanan, McCabe, Laura R.]
通讯作者:
McCabe, Laura R.
DOI:
10.1016/bs.ai.2017.05.003
发表时间:
2017
期刊:
Advances in immunology
影响因子:
--
作者:
[Steury MD, McCabe LR, Parameswaran N]
通讯作者:
Parameswaran N
DOI:
10.1007/978-3-319-66653-2_5
发表时间:
2017
期刊:
Advances in experimental medicine and biology
影响因子:
--
作者:
[Collins FL, Schepper JD, Rios-Arce ND, Steury MD, Kang HJ, Mallin H, Schoenherr D, Camfield G, Chishti S, McCabe LR, Parameswaran N]
通讯作者:
Parameswaran N
共 6 条
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Arrestins in TLR4 Signaling in Macrophages
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Arrestins in TLR4 Signaling in Macrophages
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GPCR Kinase-2 in TNFalpha Signaling in Macrophages
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Arrestins in TLR4 Signaling in Macrophages
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GPCR Kinase-2 in TNFalpha Signaling in Macrophages
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资助金额:$16.27万
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财政年份:2008
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AT1R-G蛋白/β-arrestins通路偏好性激活在急性肾损伤中的作用及其机制
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