2022 Angiotensin GRC/GRS
2022 血管紧张素 GRC/GRS
基本信息
- 批准号:10381797
- 负责人:
- 金额:$ 4万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-11-23 至 2022-10-31
- 项目状态:已结题
- 来源:
- 关键词:2019-nCoVACE2AcademiaAddressAdipose tissueAgingAngiotensin IAngiotensin IIAngiotensin ReceptorAngiotensin-Converting Enzyme InhibitorsAngiotensinsAnniversaryAreaAwardBasic ScienceBiologyBlood PressureBone MarrowCOVID-19COVID-19 pandemicCardiometabolic DiseaseCardiovascular DiseasesCardiovascular PhysiologyCardiovascular systemClinicClinicalClinical MedicineClinical SciencesCollaborationsDataDevelopmentDiabetes MellitusDigestive System DisordersDiseaseDoctor of MedicineDoctor of PhilosophyElectrolyte BalanceElectrolytesEndocrine System DiseasesEnzymesEtiologyEventFosteringFundingFutureGenderGenerationsGoalsHealthHealth SciencesHematological DiseaseHomeostasisHuman BiologyHypertensionImmune responseImmune systemIndustryInflammatory ResponseInstitutesInternationalJointsKidneyKidney DiseasesLeadLeadershipLife Cycle StagesLiquid substanceMediator of activation proteinMedical ResearchMentorsMentorshipMetabolic DiseasesMinority GroupsMissionNational Heart, Lung, and Blood InstituteNational Institute of Allergy and Infectious DiseaseNational Institute of Diabetes and Digestive and Kidney DiseasesNeurocognitionNeurosecretory SystemsNutrition DisordersObesityOrganOutcomeOxidative StressPathologic ProcessesPathologyPersonsPharmacogenomicsPopulationPostdoctoral FellowProductivityProteinsProteomicsPublic HealthQuality of lifeRegulationRenin-Angiotensin-Aldosterone SystemResearchResearch PersonnelResearch TrainingRoleSARS-CoV-2 infectionScienceScientistSex DifferencesSystemTherapeuticTissuesTranslatingTranslational ResearchTravelUnderrepresented MinorityUnderrepresented PopulationsUnited KingdomUnited States National Institutes of HealthUniversitiesUrologic DiseasesVirginiaWomanWomen Physiciansangiotensin I (1-7)armbasecareercareer developmentdesignfetal programmingfrontiergraduate studenthuman diseaseimprovedinsightliver functionmeetingsmetabolomicsminority studentnephrogenesisnovelprecision medicineprogramsreceptorreceptor functionsuccesssymposiumsystems researchtherapeutic targettoolundergraduate student
项目摘要
PROJECT SUMMARY
The renin angiotensin aldosterone system (RAAS) is a key regulator of cardiovascular (CV) function, fluid
electrolyte balance, and homeostasis, and it influences many systems including the renal, neuroendocrine, and
immune systems. Perturbations of the RAAS trigger a cascade of events, including generation of vasoactive
mediators, oxidative stress, inflammatory responses, and tissue remodeling, thus contributing to end-organ
pathology and disease. In the 2022 GRC on Ang, we will discuss the most recent, cutting-edge discoveries in
the field and share insights on emerging new areas beyond the CV system such as the role of the RAAS in
adipose biology, bone marrow regulation, liver function, neurocognition, and immune responses. The
conference will focus on the latest advances of the RAAS from discovery science to clinical impact. A highlight
in 2022 will be the celebration of 22 years of the discovery of ACE2. ACE2 is a multifunctional protein, that not
only is CV protective by generating Ang-(1-7) and Ang-(1-9) from Ang II and Ang I respectively, but it is also,
tissue injurious by acting as the receptor for the SARS-CoV-2, the etiologic agent of the current worldwide
COVID-19 pandemic. The enigmas of ACE2 as a key enzyme in the protective arm of the RAAS will be a
highlight. The role of ACE2 as a major mediator and potential therapeutic target in COVID-19 will be debated
along with the controversies on the progression of COVID-19 infection and long-term outcomes in populations
treated with ACE inhibitors and/or angiotensin receptor blockers. The 2022 GRC on Ang will further feature
novel topics including sex-differences in the regulation and changes of the RAAS during the life course (fetal
programming, kidney development, and aging) will be further addressed. In line with precision medicine being
the next frontier in clinical medicine, the meeting will also highlight new advances in the pharmacogenomics,
proteomics, and metabolomics of the RAAS in human diseases. Preceding the GRC, we will have the 2022
Gordon Research Seminar (GRS), a special forum for graduate students, postdoctoral fellows, early career
researchers and other junior scientists to present and exchange new data and cutting-edge ideas. The 2022
GRS will focus on recent advances in RAAS studies beyond the classical paradigms, including new functions
of receptors from this system and providing trainees with an enhanced understanding of current tools to aid
their research, and cover a wide range of topics including the immune system, sex differences and aging.
Additionally, the mentorship sessions will address the interplay between academia and industry and discuss
approaches to translate scientific discoveries to the clinic and how to optimize impact. The aims are aligned
with the NHLBI, NIDDK and NIAID missions and initiative and the scientific themes that will be covered are of
direct relevance to these institutes. NIH funds requested will help attract young investigators and trainees,
including from underrepresented groups with limited opportunities to joint top national and international experts
in the RAAS for networking among researchers, clinicians, young investigators and trainees.
项目总结
肾素-血管紧张素-醛固酮系统(RAAS)是心血管功能的重要调节因子。
电解质平衡和动态平衡,它影响许多系统,包括肾脏、神经内分泌和
免疫系统。RAS的扰动触发了一系列事件,包括血管活性的产生
中介物、氧化应激、炎症反应和组织重塑,从而促进终末器官
病理学和疾病。在2022年关于ANG的GRC中,我们将讨论最新的前沿发现
现场并分享对简历系统以外的新兴新领域的见解,例如RAAS在
脂肪生物学、骨髓调节、肝功能、神经认知和免疫反应。这个
会议将集中讨论RAAS从发现科学到临床影响的最新进展。一大亮点
2022年将是ACE2发现22周年的庆典。ACE2是一种多功能蛋白质,而不是
仅通过分别从Ang II和Ang I生成Ang-(1-7)和Ang-(1-9)来保护CV,但它也是,
作为SARS-CoV-2的受体对组织造成损害,SARS-CoV-2是目前全球范围内的病原体
新冠肺炎大流行。ACE2作为RAAS保护臂中的关键酶的谜团将是一个
重点。血管紧张素转换酶2在新冠肺炎中作为一个主要的介质和潜在的治疗靶点的作用将会被争论。
伴随着关于新冠肺炎感染的进展和人群长期结局的争议
用血管紧张素转换酶抑制剂和/或血管紧张素受体阻滞剂治疗。Ang上的2022年GRC将进一步
新颖的主题,包括生命过程中RAAS调节和变化的性别差异(胎儿
规划、肾脏发育和老龄化)将进一步得到解决。与精准医疗相一致
临床医学的下一个前沿,会议还将突出药物基因组学的新进展,
蛋白质组学和人类疾病中RAAS的代谢组学。在GRC之前,我们将有2022年
戈登研究研讨会(GRS),一个专门为研究生、博士后研究员、早期职业生涯举办的论坛
研究人员和其他初级科学家展示和交流新数据和前沿思想。2022年
GRS将关注RAAS研究的最新进展,超越经典范式,包括新功能
了解该系统的受体,并为受训者提供对当前辅助工具的增强理解
他们的研究涵盖了广泛的主题,包括免疫系统、性别差异和衰老。
此外,导师会议将讨论学术界和工业界之间的相互作用,并讨论
将科学发现转化为临床的方法以及如何优化影响。目标是一致的
随着NHLBI、NIDDK和NIAID的任务和倡议以及将涵盖的科学主题
与这些机构直接相关。NIH申请的资金将有助于吸引年轻的研究人员和实习生,
包括从代表性不足、机会有限的群体到联合顶级国家和国际专家
在研究人员、临床医生、年轻研究人员和受训人员之间建立网络的RAAS。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Minolfa C Prieto其他文献
Minolfa C Prieto的其他文献
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{{ truncateString('Minolfa C Prieto', 18)}}的其他基金
COVID-19 and Kidney Injury: Urinary Transcriptomics of Kidney Injury in Novel Nonhuman Primate Models of SARS-CoV-2
COVID-19 和肾损伤:SARS-CoV-2 新型非人灵长类动物模型中肾损伤的尿转录组学
- 批准号:
10453220 - 财政年份:2022
- 资助金额:
$ 4万 - 项目类别:
COVID-19 and Kidney Injury: Urinary Transcriptomics of Kidney Injury in Novel Nonhuman Primate Models of SARS-CoV-2
COVID-19 和肾损伤:SARS-CoV-2 新型非人灵长类动物模型中肾损伤的尿转录组学
- 批准号:
10689671 - 财政年份:2022
- 资助金额:
$ 4万 - 项目类别:
PLEIOTROPIC EFFECTS OF PRORENIN RECEPOR IN COLLECTING DUCT AND INTRARENAL RAS ACTIVATION
肾素原受体在收集管和肾内 RAS 激活中的多效性作用
- 批准号:
9306688 - 财政年份:2014
- 资助金额:
$ 4万 - 项目类别:
PLEIOTROPIC EFFECTS OF PRORENIN RECEPOR IN COLLECTING DUCT AND INTRARENAL RAS ACTIVATION
肾素原受体在收集管和肾内 RAS 激活中的多效性作用
- 批准号:
8800966 - 财政年份:2014
- 资助金额:
$ 4万 - 项目类别:
DISTAL NEPHRON RENIN & PRORENIN RECEPTOR IN ANG II-DEPENDANT HYPERTENSION
远端肾单位肾素
- 批准号:
8360257 - 财政年份:2011
- 资助金额:
$ 4万 - 项目类别:
DISTAL NEPHRON RENIN & PRORENIN RECEPTOR IN ANG II-DEPENDANT HYPERTENSION
远端肾单位肾素
- 批准号:
8167895 - 财政年份:2010
- 资助金额:
$ 4万 - 项目类别:
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