Targeting Myeloid Populations to Reduce Injury after Intracerebral Hemorrhage
Targeting Myeloid Populations to Reduce Injury after Intracerebral Hemorrhage
批准号:
8443189
负责人:
LAUREN H SANSING
金额:
$18.74万
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:
2012-09-01 至 2017-08-31
关键词:
AffectAgonistAnti-Inflammatory AgentsAnti-inflammatoryBloodBone MarrowBrainBrain InjuriesCCL2 geneCX3CL1 geneCellsCentral Nervous System DiseasesCerebral hemisphere hemorrhageChemotaxisChimera organismComplementConnecticutCytokine ActivationDevelopment PlansDisabled PersonsDisease modelEventFibrinogenFlow CytometryGelatinase BGoalsHealthHematopoieticHemorrhageHourImmuneImmune responseImmune systemImmunohistochemistryImmunologyIndividualInfiltrationInflammationInflammation MediatorsInflammatoryInflammatory InfiltrateInflammatory ResponseInjuryInvestigationIronIschemic StrokeKnockout MiceLeadLeftLeukocytesLong-Term EffectsMeasuresMediatingMentorsMicrogliaModelingMusMyelogenousMyeloid CellsNeurologyNeuronsNeurosciencesNeutrophil ActivationOutcomePathway interactionsPatientsPhagocytosisPopulationPositioning AttributeProductionReceptor ActivationRecombinantsRecoveryResearchResearch PersonnelResearch Project GrantsRiskRoleSignal TransductionSiteStaining methodStainsStimulusStrokeTestingTherapeutic InterventionThrombinTimeTrainingTransgenic MiceUniversitiesWestern BlottingWorkcareercareer developmentcell typechemokinechemokine receptorcytokinedisabilityfunctional disabilityfunctional outcomesgait examinationimprovedin vitro Assayin vivomonocyteneurobehavioralneuroprotectionprofessorprogenitorreceptorresponsesymposiumtherapeutic targettoll-like receptor 4trafficking
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Intracerebral hemorrhage (ICH) is a devastating type of stroke affecting more than 70,000 patients in the U.S. each year, yet there is no specific treatment available. Stimulation of the innate immune system at the site of hemorrhage leads to inflammation and progressive brain injury. In a murine model of ICH, we have demonstrated that ICH leads to the recruitment of blood-derived monocytes and inflammatory monocytes to the perihematomal region and the activation and proliferation of microglia. These events are concomitant with progressive functional disability. The proposed studies will utilize transgenic mice, bone marrow chimeras, and in vitro assays to determine the individual effects of each population on the immune response and functional outcomes after ICH. Specific Aim 1 will determine the roles of the CX3CR1+ and CCR2+Gr1+ monocyte populations in injury after ICH. In Specific Aim 2, the role of chemokine receptors CX3CR1 and CCR2 on microglial activation will be investigated. Together these studies will determine the translational potential of targetin these cellular responses in the treatment of ICH. This proposal outlines the training of Lauren Sansing, MD, an Assistant Professor in Neurology at the University of Connecticut Health Center, from mentored to independent translational researcher. Career development plans include formal coursework in immunology, regular seminar attendance in both immunology and neuroscience, and conference participation. These didactic components will complement the training involved in executing the research project and optimally position Dr. Sansing for a career as an independent investigator in translational stroke research.
PUBLIC HEALTH RELEVANCE: Intracerebral hemorrhage is a type of stroke that affects 70,000 people in the U.S. each year and causes half of the patients to die or be left severely disabled. This proposal will study the immune pathways responsible for brain injury surrounding the hemorrhage and hopes to identify new targets for treatment.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Y-SPAN: Yale Translational Cerebroprotection Program in SPAN
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批准号:10590809
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项目类别:
-
资助金额:$66.95万
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财政年份:2023
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负责人:LAUREN H SANSING
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依托单位:
Manipulation of metabolic pathways to enhance human macrophage phenotypes after ICH
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批准号:10155994
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项目类别:
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资助金额:$20.94万
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财政年份:2020
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负责人:LAUREN H SANSING
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依托单位:
Manipulation of metabolic pathways to enhance human macrophage phenotypes after ICH
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批准号:10308104
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项目类别:
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资助金额:$25.13万
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财政年份:2020
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负责人:LAUREN H SANSING
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依托单位:
Yale site for Stroke Preclinical Assessment Network (SPAN) for Acute Neuroprotection
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批准号:10216372
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项目类别:
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资助金额:$53.62万
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财政年份:2019
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负责人:LAUREN H SANSING
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依托单位:
Efferocytosis and the resolution of inflammation after intracerebral hemorrhage
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批准号:9335992
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项目类别:
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资助金额:$36.64万
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财政年份:2016
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负责人:LAUREN H SANSING
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依托单位:
Efferocytosis and the resolution of inflammation after intracerebral hemorrhage
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批准号:9752671
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项目类别:
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资助金额:$36.64万
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财政年份:2016
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负责人:LAUREN H SANSING
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依托单位:
Dynamic Neuroimmune Profiling in Patients with Acute Intracerebral Hemorrhage
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批准号:9156547
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项目类别:
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资助金额:$63.62万
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财政年份:2016
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负责人:LAUREN H SANSING
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依托单位:
Targeting Myeloid Populations to Reduce Injury after Intracerebral Hemorrhage
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批准号:8970204
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项目类别:
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资助金额:$18.89万
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财政年份:2014
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负责人:LAUREN H SANSING
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依托单位:
Modulating Monocyte Responses to Reduce Injury after Intracerebral Hemorrhage
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批准号:8919473
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项目类别:
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资助金额:$20.81万
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财政年份:2014
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负责人:LAUREN H SANSING
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依托单位:
Targeting Myeloid Populations to Reduce Injury after Intracerebral Hemorrhage
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批准号:8901319
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项目类别:
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资助金额:$18.74万
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财政年份:2014
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负责人:LAUREN H SANSING
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依托单位:
Modulating Monocyte Responses to Reduce Injury after Intracerebral Hemorrhage
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批准号:8772759
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项目类别:
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资助金额:$24.98万
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财政年份:2014
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负责人:LAUREN H SANSING
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依托单位:
Targeting Myeloid Populations to Reduce Injury after Intracerebral Hemorrhage
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批准号:8535853
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项目类别:
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资助金额:$18.74万
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财政年份:2012
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负责人:LAUREN H SANSING
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依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
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批准号:32000851
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项目类别:青年科学基金项目
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资助金额:24.0万元
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批准年份:2020
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负责人:乔安娜
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依托单位: