The Role of Family with Sequence Similarity 3D (FAM3D) in Cardioprotection and Inflammation after Myocardial Infarction
The Role of Family with Sequence Similarity 3D (FAM3D) in Cardioprotection and Inflammation after Myocardial Infarction
批准号:
10320371
负责人:
James Rhee
金额:
$17.28万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-01-15 至 2023-12-31
关键词:
3-DimensionalAcuteAcute myocardial infarctionAddressAdvisory CommitteesAnesthesia proceduresAnimal ModelAnti-Inflammatory AgentsApoptosisAttenuatedBindingCardiacCardiac MyocytesCardiologyCardiovascular DiseasesCardiovascular systemCause of DeathCell SeparationCell SurvivalCellsCharacteristicsChronicClinicalClinical TrialsCollaborationsComplexCongenic MiceCritical CareDataDevelopmentDevelopment PlansDoctor of MedicineDoctor of PhilosophyEchocardiographyEnvironmentEquilibriumEventFacultyFamilyFibrosisFlow CytometryGene Expression ProfileGeneral HospitalsHealth PromotionHeartHeart DiseasesHeart InjuriesHeart failureHistologicHomeostasisHypertrophyImageImmuneImpairmentInfarctionInflammationInjuryInvestigationLeadershipLeft Ventricular FunctionLeukocyte TraffickingLeukocytesLinkMassachusettsMeasuresMediatingMedicineMentorsMentorshipModelingMolecularMolecular AnalysisMolecular and Cellular BiologyMorbidity - disease rateMouse StrainsMusMyocardialMyocardial InfarctionMyocardial IschemiaMyocardial ReperfusionMyocarditisMyocardiumOrganPTPRC genePathway interactionsPatientsPerfusionPlasmaPlasma ProteinsPlayPopulationPositioning AttributePrincipal InvestigatorProcessProteinsProteomicsRecombinant ProteinsRecombinantsRecoveryReperfusion InjuryReperfusion TherapyResearchResearch PersonnelResearch ProposalsRiskRoleSamplingScientistSorting - Cell MovementSpleenSplenocyteStressSystemSystems BiologyTestingTimeTissuesTroponinTweensUnited StatesValidationVascular EndotheliumViralaptamerbasebiomarker discoverybiomarker validationcardioprotectioncardiovascular healthcareer developmentcell injurycell typechemokinecytokineexperiencefMet-Leu-Phe receptorgain of functionhealingheart functionimaging programimmune activationimmunoregulationimprovedin vivoinsightinstructorischemic injuryloss of functionmedical schoolsmembermid-career facultymonocytemortalitymyocardial injuryneutralizing antibodyneutrophilnovelnovel therapeuticsoverexpressionpreservationpreventprofessorprogramsrecruitresponse
中文摘要
项目总结/摘要:
本研究提案概述了James Rhee,M.D.的5年职业发展计划,哲学博士、重新表示
马萨诸塞州总医院心血管研究中心的研究员和讲师
在麻醉在哈佛医学院(HMS),以实现独立的主要研究者根据
安东尼·罗森茨威格博士的指导,MGH心脏病学主任和HMS医学教授。我-
重要的是,罗森茨威格博士有指导科学家的良好记录,有50多名学员持有aca,
学院教职,许多人担任领导职务。由一濑文人、Pro.
HMS教授; Jianren Mao,研究副主席;和Saumya Das,医学副教授,
沿着与Matthias Nazodorf博士(系统中心小鼠成像项目主任)的合作,
tems生物学),将提供生物标志物发现和验证,心脏应激和炎症模型的专业知识,
信息和成像,以及职业发展。李博士将充分利用世界一流的环境
罗森茨威格实验室和周围的MGH和哈佛医学院校园在解决ambi-
这一提议的目的。该计划使Rhee博士能够发展心血管蛋白质组学方面的专业知识,
缺血再灌注损伤,建立在他在细胞和分子生物学的长期研究经验
以及他在重症监护中的临床作用。
损伤后心脏的保护和有效适应或“重塑”是一个复杂的过程
涉及心肌细胞和许多其他细胞类型之间的串扰。在清算死亡或
损伤的细胞,并增强存活的心脏和非心脏组织,如血管内膜,
Thorax是维持体内平衡和恢复功能所必需的。最佳的心肌重塑-
损伤后的免疫系统在很大程度上依赖于免疫程序的适当顺序激活,
白细胞的不同亚型。候选人已经使用了来自“好”和“差”重塑者的血浆样本
以确定可能限制急性损伤和促进愈合的分泌因子。的
超过1300种循环蛋白质,是得分最高的候选者之一,通过两种统计学显著性,
趋化因子FAM 3D是具有序列相似性的趋化因子家族3成员D(FAM 3D)。提出
这一提议是令人信服的初步数据,表明脾FAM 3D发挥急性保护作用,在
缺血再灌注损伤后,通过抗炎机制,
nisms。Rhee博士制定了一个全面的计划来描述完全新颖的心血管影响,
这个分子。他将采用强有力的体内功能获得和丧失研究,以更好地了解
FAM3D。这些研究将有助于更好地了解缺血性损伤和随之而来的炎症,
以及如何限制和治疗心脏和其他重要器官中的这些疾病的新的治疗见解。
英文摘要
PROJECT SUMMARY / ABSTRACT:
This research proposal outlines a 5-year career development plan for James Rhee, M.D., Ph.D., re-
search fellow at the Cardiovascular Research Center at Massachusetts General Hospital (MGH) and Instructor
in Anesthesia at Harvard Medical School (HMS), to achieve independence as a principal investigator under the
mentorship of Anthony Rosenzweig, M.D., Chief of Cardiology at MGH and Professor of Medicine at HMS. Im-
portantly, Dr. Rosenzweig has a strong track record of mentoring scientists with over 50 trainees holding aca-
demic faculty positions, many in leadership roles. An advisory committee composed of Fumito Ichinose, Pro-
fessor at HMS; Jianren Mao, Vice-Chair of Research; and Saumya Das, Associate Professor of Medicine,
along with collaboration from Dr. Matthias Nahrendorf (Director of the Mouse Imaging Program, Center for Sys-
tems Biology), will lend expertise on models of biomarker discovery and validation, cardiac stress and inflam-
mation and imaging, and career development. Dr. Rhee will take full advantage of the world class environment
of the Rosenzweig lab and surrounding MGH and Harvard Medical School campuses in addressing the ambi-
tious aims of this proposal. This plan allows Dr. Rhee to develop expertise in cardiovascular proteomics and
ischemia reperfusion injury that builds upon his lengthy research experiences in cellular and molecular biology
and his clinical role in the critical care of high acuity patients.
Cardioprotection and effective adaptation or “remodeling” of the heart after injury is a complex process
involving cross-talk between cardiomyocytes and many other cell types. A balance between clearing dead or
damaged cells and enhancing the viability of surviving cardiac and non-cardiac tissue, such as vascular endo-
thelium, is essential for maintaining homeostasis and recovering function. Optimal remodeling of the myocardi-
um after injury is largely dependent on appropriate sequential activation of an immune program involving dif-
ferent subtypes of leukocytes. The candidate has used plasma samples from “good” and “poor” remodelers
after myocardial infarction to identify secreted factors that may limit acute injury and promote healing. Of the
more than 1300 circulating proteins profiled, one of the highest scoring candidates, by both statistical signifi-
cance and fold change, is the chemokine Family with sequence similarity 3 member D (FAM3D). Presented in
this proposal are compelling preliminary data to suggest that splenic FAM3D exerts acute protection, in the
form of dramatically reduced infarct size, after ischemia-reperfusion injury through anti-inflammatory mecha-
nisms. Dr.Rhee lays out a comprehensive plan to characterize the completely novel cardiovascular impact of
this molecule. He will employ robust in vivo gain- and loss-of-function studies to better understand the role of
FAM3D. These studies will lead to a better understanding of ischemic injury and the ensuing inflammation,
and to new therapeutic insight into how to limit and treat these conditions in the heart and other vital organs.
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The Role of Family with Sequence Similarity 3D (FAM3D) in Cardioprotection and Inflammation after Myocardial Infarction
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批准号:10549297
-
项目类别:
-
资助金额:$17.28万
-
财政年份:2019
-
负责人:James Rhee
-
依托单位:
The Role of Family with Sequence Similarity 3D (FAM3D) in Cardioprotection and Inflammation after Myocardial Infarction
-
批准号:10080365
-
项目类别:
-
资助金额:$17.28万
-
财政年份:2019
-
负责人:James Rhee
-
依托单位:
海外基金