Ubiquitylation and the Regulation of Immune Homeostasis
Ubiquitylation and the Regulation of Immune Homeostasis
批准号:
8008665
负责人:
Robert Cohen
金额:
$60.83万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-01 至 2015-08-31
关键词:
A20 proteinAllelesAnti-Inflammatory AgentsAnti-inflammatoryAntigensBindingBiochemicalBiochemistryC-terminalCell physiologyCellsCellular biologyCleaved cellCysteineDendritic CellsDiseaseEnzymesExhibitsGene TargetingGenesGoalsHomeostasisITGAX geneImmuneImmune responseIn VitroInflammatoryKnock-in MouseLaboratoriesLigandsLinkMediatingMouse StrainsMusMutationN-terminalNatural ImmunityPhysiologicalPlayPolyubiquitinProteinsPublic HealthReagentReceptor SignalingRecruitment ActivityRegulationRoleSignal PathwaySignal TransductionSignaling ProteinSpecificityTNF geneTRAF6 geneToll-like receptorsTransgenic MiceUbiquitinUbiquitinationWorkZinc Fingersin vivonovelperipheral toleranceprotein protein interactionpublic health relevanceresponsetherapy developmentubiquitin isopeptidaseubiquitin-protein ligase
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Dendritic cells (DCs) are innate immune cells that regulate both immune homeostasis as well as antigen driven immune responses. The functions of DCs are highly regulated by signals initiated by Toll-like receptors (TLRs). Consequently, intracellular molecules that regulate TLR signaling pathways are pivotal for regulating host immune responses. We have recently found that A20 is a ubiquitin modifying enzyme that restricts toll-like receptor (TLR) induced signals. We are studying the roles of A20 expression in DCs in regulating immune homeostasis and responses. To accomplish this, we have generated two strains of gene targeted mice: one that disrupts the A20 gene in all cells and one in which a "floxed" allele of A20 has been targeted to the endogenous A20 locus. We have interbred the "floxed" mice with a novel strain of CD11-Cre transgenic mouse line that expresses Cre enzyme with high selectivity and specificity in DCs. These compound A20flox/flox CD11c-Cre mice will thus provide us with a very powerful and novel reagent for studying the role of A20 expression in DCs in regulating immune homeostasis and immune responses. We propose to use these A20flox/flox CD11-cre compound mice, as well as cells derived from both strains of mice, to determine how A20 expression in DCs regulates their responses to TLR ligands in vitro and in vivo. The first aim will focus upon understanding the cell biology and biochemistry underlying A20's roles in regulating TLR signaling in DCs, and will elucidate the cell-autonomous functions of DCs that are regulated by A20. The second aim will utilize A20flox/flox CD11c-Cre mice to determine how A20 expression in DCs regulates their homeostasis and activation in vivo. This second aim will also interrogate how A20 expression in DCs regulates peripheral tolerance and immune responses.
PUBLIC HEALTH RELEVANCE: This project focuses on a potent endogenous anti-inflammatory protein called A20, and how it regulates dendritic cell functions in vivo. As dendritic cells are powerful regulators of immune responses, and as A20 plays critical roles in regulating dendritic cell functions, understanding how A20 regulates dendritic cells and immune responses could significantly enhance the development of therapies for inflammatory diseases and thus have major benefits for public health.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Detection and quantitation of branched ubiquitin in polyubiquitinated proteins
-
批准号:10058026
-
项目类别:
-
资助金额:$22.5万
-
财政年份:2020
-
负责人:Robert Cohen
-
依托单位:
Detection and quantitation of branched ubiquitin in polyubiquitinated proteins
-
批准号:10261524
-
项目类别:
-
资助金额:$18.94万
-
财政年份:2020
-
负责人:Robert Cohen
-
依托单位:
Quantitation of Ubiquitin Dynamics and Homeostasis
-
批准号:8945431
-
项目类别:
-
资助金额:$47.7万
-
财政年份:2015
-
负责人:Robert Cohen
-
依托单位:
Quantitation of Ubiquitin Dynamics and Homeostasis
-
批准号:9315902
-
项目类别:
-
资助金额:$44.88万
-
财政年份:2015
-
负责人:Robert Cohen
-
依托单位:
Quantitation of Ubiquitin Dynamics and Homeostasis
-
批准号:9274672
-
项目类别:
-
资助金额:$15.84万
-
财政年份:2015
-
负责人:Robert Cohen
-
依托单位:
Quantitation of Ubiquitin Dynamics and Homeostasis
-
批准号:9134801
-
项目类别:
-
资助金额:$45.0万
-
财政年份:2015
-
负责人:Robert Cohen
-
依托单位:
Linkage-specific recognition of polyubiquitin
-
批准号:8320942
-
项目类别:
-
资助金额:$27.77万
-
财政年份:2011
-
负责人:Robert Cohen
-
依托单位:
Linkage-specific recognition of polyubiquitin
-
批准号:8479378
-
项目类别:
-
资助金额:$27.14万
-
财政年份:2011
-
负责人:Robert Cohen
-
依托单位:
Linkage-specific recognition of polyubiquitin
-
批准号:8668081
-
项目类别:
-
资助金额:$28.11万
-
财政年份:2011
-
负责人:Robert Cohen
-
依托单位:
Linkage-specific recognition of polyubiquitin
-
批准号:8085954
-
项目类别:
-
资助金额:$25.54万
-
财政年份:2011
-
负责人:Robert Cohen
-
依托单位:
Capture of Ubiquitin Conjugation and Deconjugation Enzyme Substrates
-
批准号:7939805
-
项目类别:
-
资助金额:$35.0万
-
财政年份:2009
-
负责人:Robert Cohen
-
依托单位:
Capture of Ubiquitin Conjugation and Deconjugation Enzyme Substrates
-
批准号:7825747
-
项目类别:
-
资助金额:$32.5万
-
财政年份:2009
-
负责人:Robert Cohen
-
依托单位:
Ubiquitylation and the Regulation of Immune Homeostasis
-
批准号:8536787
-
项目类别:
-
资助金额:$46.74万
-
财政年份:2005
-
负责人:Robert Cohen
-
依托单位:
Ubiquitylation and the Regulation of Immune Homeostasis
-
批准号:8728194
-
项目类别:
-
资助金额:$48.39万
-
财政年份:2005
-
负责人:Robert Cohen
-
依托单位:
Ubiquitylation and the Regulation of Immune Homeostasis
-
批准号:8124933
-
项目类别:
-
资助金额:$48.78万
-
财政年份:2005
-
负责人:Robert Cohen
-
依托单位:
Ubiquitylation and the Regulation of Immune Homeostasis
-
批准号:8327270
-
项目类别:
-
资助金额:$48.78万
-
财政年份:2005
-
负责人:Robert Cohen
-
依托单位:
海外基金