Role of FSTL-1 in Arthritis
Role of FSTL-1 in Arthritis
批准号:
7513342
负责人:
Raphael Hirsch
金额:
$37.88万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2012-06-30
关键词:
AccountingAdenovirusesAntibodiesArthritisAutoimmunityB-LymphocytesCD4 Positive T LymphocytesCartilageCell Surface ReceptorsCellsCollagen ArthritisCollagen Type IIConditionDNA Microarray ChipDNA Microarray formatDiseaseFibroblastsFollistatinGene ExpressionGene TransferGenesIn VitroInflammationInflammatoryInterleukin-17Interleukin-6JointsKnock-outLeadMediatingMusOsteoblastsPathway interactionsPatientsPlayPropertyProtein OverexpressionProteinsPublic HealthRegulationRheumatoid ArthritisRoleSignal TransductionSourceStagingSwellingT-Cell ReceptorT-Lymphocyte SubsetsTestingThinkingTissuesUp-Regulationbonecofactorin vivonovelnovel therapeuticsresponsetherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): While performing a DNA microarray gene expression analysis in collagen-induced arthritis (CIA), we discovered that a poorly-characterized gene, follistatin-like 1 (FSTL-1), was highly overexpressed in mouse paws during the early stages of arthritis. Especially-high expression was observed at the interface of synovial pannus and eroding bone, suggesting a role in joint destruction. Our Preliminary Studies provide strong evidence for a role for FSTL-1 in arthritis. Over-expression of FSTL-1 in mice resulted in severe paw swelling and arthritis, while neutralization of endogenous FSTL-1 ameliorated arthritis. We have also observed elevated expression of FSTL-1 in synovial tissues of patients with rheumatoid arthritis. Finally, we have now made the surprising observation that FSTL-1 induces maturation of IL-17-producing Th17 cells from naove CD4+ T cells. This finding represents a novel pathway for induction of Th17 cells, which have recently been shown to play a central role in autoimmunity, and whose maturation had previously been thought to require IL- 6 and TGF-. The current application will test the hypothesis that FSTL-1 plays a central role in arthritis and will explore the possibility that neutralization of FSTL-1 represents a novel therapeutic approach to the treatment of arthritis. The first Specific Aim is to determine the mechanism by which FSTL-1 induces inflammation. We will determine how FSTL-1 induces Th17 cells in vitro, whether FSTL-1 acts by a T cell receptor-dependent or independent pathway, whether FSTL-1 mediates its effect through a cell surface receptor, the FSTL-1 domain(s) responsible for the activity of FSTL-1 and whether FSTL-1 induces Th17 cells in vivo. The second Specific Aim is to determine the factors regulating FSTL-1 expression, including the tissue and cellular sources of FSTL-1 and the signals that induce FSTL-1 expression. The third Specific Aim is to determine the role of FSTL-1 in arthritis by overexpressing it, by neutralizing it in vivo with antibodies as well as by creating a conditional knockout. Understanding the properties of this novel protein will result in a better understanding of arthritis and possibly lead to new therapeutic targets. PUBLIC HEALTH RELEVANCE We have discovered a protein that plays a novel role in arthritis. Characterization of the properties of this protein is likely to lead to a better understanding of arthritis and possibly new therapies.
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会议论文
The Child Health Research Career Development Program at UCSF
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批准号:10610824
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项目类别:
-
资助金额:$35.06万
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财政年份:2021
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负责人:Raphael Hirsch
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依托单位:
The Child Health Research Career Development Program at UCSF
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批准号:10224603
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项目类别:
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资助金额:$44.5万
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财政年份:2021
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负责人:Raphael Hirsch
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依托单位:
The Child Health Research Career Development Program at UCSF
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批准号:10374909
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项目类别:
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资助金额:$44.5万
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财政年份:2021
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负责人:Raphael Hirsch
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依托单位:
Role of FSTL-1 in Arthritis
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批准号:8116805
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项目类别:
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资助金额:$8.14万
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财政年份:2010
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负责人:Raphael Hirsch
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依托单位:
USE OF THERMAL AND 3D IMAGING TO QUANTIFY ARTHRITIS
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批准号:7567325
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项目类别:
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资助金额:$17.87万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
Characterization of a novel T cell activating protein in arthritis
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批准号:7624847
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项目类别:
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资助金额:$33.33万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
USE OF THERMAL AND 3D IMAGING TO QUANTIFY ARTHRITIS
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批准号:7806547
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项目类别:
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资助金额:$20.55万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
Characterization of a novel T cell activating protein in arthritis
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批准号:7774332
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项目类别:
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资助金额:$33.0万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
Characterization of a novel T cell activating protein in arthritis
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批准号:8212554
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项目类别:
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资助金额:$14.25万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
Characterization of a novel T cell activating protein in arthritis
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批准号:8435422
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项目类别:
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资助金额:$29.99万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
Characterization of a novel T cell activating protein in arthritis
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批准号:8018492
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项目类别:
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资助金额:$31.68万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
Characterization of a novel T cell activating protein in arthritis
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批准号:8495522
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项目类别:
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资助金额:$17.37万
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财政年份:2009
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负责人:Raphael Hirsch
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依托单位:
Role of FSTL-1 in Arthritis
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批准号:7645016
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项目类别:
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资助金额:$37.88万
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财政年份:2008
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负责人:Raphael Hirsch
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依托单位:
Role of FSTL-1 in Arthritis
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批准号:8085884
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项目类别:
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资助金额:$37.12万
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财政年份:2008
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负责人:Raphael Hirsch
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依托单位:
Role of FSTL-1 in Arthritis
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批准号:7897778
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项目类别:
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资助金额:$37.5万
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财政年份:2008
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负责人:Raphael Hirsch
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依托单位:
PITTSBURGH PEDIATRIC RHEUMATOLOGY TRAINING GRANT
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批准号:6894142
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项目类别:
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资助金额:$10.98万
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财政年份:2005
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负责人:Raphael Hirsch
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依托单位:
Pittsburgh Pediatric Rheumatology Training Grant
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批准号:7849173
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项目类别:
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资助金额:$12.78万
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财政年份:2005
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负责人:Raphael Hirsch
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依托单位:
PITTSBURGH PEDIATRIC RHEUMATOLOGY TRAINING GRANT
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批准号:7060406
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项目类别:
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资助金额:$22.13万
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财政年份:2005
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负责人:Raphael Hirsch
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依托单位:
PITTSBURGH PEDIATRIC RHEUMATOLOGY TRAINING GRANT
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批准号:7415246
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项目类别:
-
资助金额:$18.94万
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财政年份:2005
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负责人:Raphael Hirsch
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依托单位:
Pittsburgh Pediatric Rheumatology Training Grant
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批准号:8067905
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项目类别:
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资助金额:$21.28万
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财政年份:2005
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负责人:Raphael Hirsch
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依托单位:
海外基金