Identification of novel genes as being important for neutrophil functions
Identification of novel genes as being important for neutrophil functions
批准号:
8300322
负责人:
Dianqing Wu
金额:
$24.87万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-02-01 至 2014-01-31
关键词:
AdherenceArthritisBacteriaBacterial InfectionsBiological AssayBiologyBone Marrow CellsCause of DeathCell PolarityCell physiologyCellsChemotaxisChronic Obstructive Airway DiseaseClinicalDefectDiseaseEndotheliumExtravasationFutureGene ExpressionGene SilencingGenerationsGenesGoalsHL60Hearing problemHomologous GeneImmune responseIn VitroInfectionInfiltrationInflammationInflammatoryInflammatory ResponseIngestionIntensive Care UnitsInvestigationKnockout MiceKnowledgeLeadLifeMammalian CellMethodsModelingMusMyeloid CellsMyeloid LeukemiaNatural ImmunityNeutrophil InfiltrationPhagocytesPhenotypePlayProteinsRegulationReperfusion InjuryResearchRetroviridaeRheumatoid ArthritisRoleSepsisSepsis SyndromeSiteStudy modelsSystemTestingTimeTissuesTransfectionTransplantationWorkbactericidebasecell motilitycell typecostdesigndirectional cellhuman diseasein vitro Assayin vivoknock-downloss of functionmacrophagemonocytemortalityneutrophilnew therapeutic targetnovelprotein expressionprotein functionsmall hairpin RNAvector
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Neutrophils are highly specialized cells in the host innate immune response that play a pivotal role in the clearance of bacterial infections and host inflammatory responses. Defects or overactivity in these cells can lead to life-threatening or debilitating diseases including sepsis, ischemia/reperfusion injury, rheumatoid arthritis, and chronic obstructive pulmonary disease (COPD). In addition, neutrophils are an excellent model for studying the mechanisms of cell polarization and directional cell migration for they are the fastest moving mammalian cells with overt cell polarity. Although a vast amount of work has been done, there are still many aspects of neutrophil biology that remain unclear. In addition, our gene expression analysis revealed a large number of proteins that are highly expressed in neutrophils, but with little knowledge about their roles in neutrophil biology. Unlike other phagocytes such as macrophages, primary differentiated neutrophils cannot be grown in culture for long and are not amenable to many of the in vitro manipulations. The majority of loss of function studies relies on targeted gene inactivation in mice or use neutrophil-like cells that difer from primary neutrophils in many regards and cannot be used for in vivo studies. To accelerate neutrophil research, we have developed a system that allows high expression of shRNAs in primary neutrophils in mice. The approach is amenable for a number of in vivo and in vitro assays for determining the importance of target proteins on various aspects of neutrophil biology. In this exploratory R21 proposal, we plan to screen targets that have no clear role in neutrophil biology or any biology. Our study will lead to identifying new proteins that play key roles in innate immunity and the inflammatory response and shed new lights into neutrophil biology, thus rapidly expanding the understanding of how neutrophils are regulated and undertake their cellular functions. Because many of the targets we propose to work on have homologs that are expressed in other tissues and cell type, our proposed studies may have potential impacts beyond neutrophils.
PUBLIC HEALTH RELEVANCE: Neutrophils play important roles in the host innate immune response and are involved in a number of human diseases including sepsis, hear diseases, arthritis, and chronic obstructive pulmonary disease (COPD). This study is to provide better understanding of the regulation of neutrophils and their roles in these diseases. Our study may provide new therapeutic targets for treating these diseases.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A novel signaling mechanism for LRP5
-
批准号:10706591
-
项目类别:
-
资助金额:$53.56万
-
财政年份:2022
-
负责人:Dianqing Wu
-
依托单位:
A novel signaling mechanism for LRP5
-
批准号:10527478
-
项目类别:
-
资助金额:$54.65万
-
财政年份:2022
-
负责人:Dianqing Wu
-
依托单位:
Signaling mechanisms and functions related to patho-physiology of vascular, lung and blood systems
-
批准号:9244290
-
项目类别:
-
资助金额:$91.23万
-
财政年份:2017
-
负责人:Dianqing Wu
-
依托单位:
DKK2 regulates NK activation and tumor immunity
-
批准号:10064071
-
项目类别:
-
资助金额:$51.33万
-
财政年份:2017
-
负责人:Dianqing Wu
-
依托单位:
Signaling mechanisms and functions related to patho-physiology of vascular, lung and blood systems
-
批准号:10570974
-
项目类别:
-
资助金额:$91.23万
-
财政年份:2017
-
负责人:Dianqing Wu
-
依托单位:
DKK2 regulates NK activation and tumor immunity
-
批准号:10307994
-
项目类别:
-
资助金额:$50.3万
-
财政年份:2017
-
负责人:Dianqing Wu
-
依托单位:
Signaling mechanisms and functions related to patho-physiology of vascular, lung and blood systems
-
批准号:10089468
-
项目类别:
-
资助金额:$91.23万
-
财政年份:2017
-
负责人:Dianqing Wu
-
依托单位:
Sustained signaling for fibroblast migration
-
批准号:9066227
-
项目类别:
-
资助金额:$41.63万
-
财政年份:2013
-
负责人:Dianqing Wu
-
依托单位:
Sustained signaling for fibroblast migration
-
批准号:8594750
-
项目类别:
-
资助金额:$39.63万
-
财政年份:2013
-
负责人:Dianqing Wu
-
依托单位:
Sustained signaling for fibroblast migration
-
批准号:8707850
-
项目类别:
-
资助金额:$40.79万
-
财政年份:2013
-
负责人:Dianqing Wu
-
依托单位:
Identification of novel genes as being important for neutrophil functions
-
批准号:8415495
-
项目类别:
-
资助金额:$20.79万
-
财政年份:2012
-
负责人:Dianqing Wu
-
依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
-
批准号:8199731
-
项目类别:
-
资助金额:$48.9万
-
财政年份:2011
-
负责人:Dianqing Wu
-
依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
-
批准号:8695455
-
项目类别:
-
资助金额:$48.2万
-
财政年份:2011
-
负责人:Dianqing Wu
-
依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
-
批准号:8504529
-
项目类别:
-
资助金额:$46.83万
-
财政年份:2011
-
负责人:Dianqing Wu
-
依托单位:
Signaling Mechanisms for Leukocyte Migration Regulation
-
批准号:8319373
-
项目类别:
-
资助金额:$49.04万
-
财政年份:2011
-
负责人:Dianqing Wu
-
依托单位:
Chemoattactant signaling, macrophage functions and atherogenesis
-
批准号:8150051
-
项目类别:
-
资助金额:$42.13万
-
财政年份:2010
-
负责人:Dianqing Wu
-
依托单位:
Wnt signaling
-
批准号:8019088
-
项目类别:
-
资助金额:$37.72万
-
财政年份:2009
-
负责人:Dianqing Wu
-
依托单位:
Wnt signaling
-
批准号:8212562
-
项目类别:
-
资助金额:$37.52万
-
财政年份:2009
-
负责人:Dianqing Wu
-
依托单位:
Wnt signaling
-
批准号:8445308
-
项目类别:
-
资助金额:$35.1万
-
财政年份:2009
-
负责人:Dianqing Wu
-
依托单位:
Investigation of the role of AMP-activated protein kinase alpha2 (AMPKa2) in bone
-
批准号:7685852
-
项目类别:
-
资助金额:$5.09万
-
财政年份:2009
-
负责人:Dianqing Wu
-
依托单位:
国内基金
海外基金
Autoimmune diseases therapies: variations on the microbiome in rheumatoid arthritis
-
批准号:31171277
-
项目类别:面上项目
-
资助金额:60.0万元
-
批准年份:2011
-
负责人:Christine Nardini
-
依托单位:
Molecular Interaction Reconstruction of Rheumatoid Arthritis Therapies Using Clinical Data
-
批准号:31070748
-
项目类别:面上项目
-
资助金额:34.0万元
-
批准年份:2010
-
负责人:Christine Nardini
-
依托单位: