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Actions of ACE2 along with Nephron to Regulate Blood Pressure

ACE2 与肾单位一起调节血压的作用

基本信息

批准号：
10646425
负责人：
Susan Bailey Gurley
金额：
$ 11.93万
依托单位：
OREGON HEALTH & SCIENCE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-04-01 至 2023-09-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10646425
关键词：
2019-nCoV ACE2 Acute Renal Failure with Renal Papillary Necrosis Address Affect Affinity Angiotensin II Animal Model Attenuated Blood Blood Pressure Blood Vessels Brush Border COVID-19 COVID-19 complications Cardiovascular Diseases Cells Coupled Data Development Disease Endothelial Cells Equilibrium Excretory function Female Filtration Gene Targeting Goals Homeostasis Hypertension Infusion procedures Kidney Knockout Mice Knowledge Length Mass Spectrum Analysis Membrane Metalloproteases Micropuncture Modeling Molecular Mus Mutate Natriuresis Nephrons Pathogenesis Pathway interactions Patients Peptides Persons Phase Phenotype Physiological Play Predisposition Proximal Kidney Tubules Receptor, Angiotensin, Type 1 Renal function Renin-Angiotensin System Resistance Role Sampling Serum Source Techniques Testing Tissues Transplantation Tubular formation Urine Virus Work blood pressure control blood pressure elevation blood pressure reduction blood pressure regulation cell type defined contribution experimental study glomerular filtration hypertension treatment hypertensive improved male member multi-photon nanoscale novel receptor solute urinary

项目摘要

Project Summary Hypertension affects more than 60 million people in the US and despite its diverse causes, blockade of the renin-angiotensin system (RAS) lowers blood pressure in the majority of hypertensive patients. ACE2 is the newest member of the RAS, and our previous work has established that ACE2 protects against hypertension with actions in the kidney to metabolize angiotensin II, thus regulating the RAS. As part of our overall goal of understanding how the RAS impacts BP, we have employed cell-specific gene-targeting and kidney cross- transplantation in mice to identify the key cellular sources of ACE2 for BP regulation. We found that mice lacking ACE2 specifically from the proximal tubule (PTACE2KO), the cell type with highest expression of ACE2 in the kidney, have exaggerated BP elevation in the early phase of angiotensin II hypertension, associated with enhanced accumulation of angiotensin II peptide in kidney and ≈50% reduction in urinary excretion of sACE2. Based on kidney cross- transplantation experiments, the development of hypertension was associated with significant reductions in sACE2 in both serum and urine whereas sACE2 appeared to normalize BP in mice lacking renal expression. Thus, our findings suggest ACE2 originating from the PT of the kidney plays a key role in the initiation of angiotensin II-dependent hypertension, and that kidney and systemic tissues both contribute to sACE2 in urine. Our new data expand knowledge of how ACE2 can impact the RAS and BP. This revised proposal aims to define molecular mechanisms contributing to hypertension in PTACE2KO mice; establish relative contribution of extra-renal ACE2 and shedding to BP regulation and vascular function with new animal models; and delineate mechanism by which ACE2 reaches the lumen of the nephron to balance the RAS. We anticipate our studies will shift the existing paradigm around how ACE2 functions to regulate BP and moderate kidney function with high relevance to disease states where ACE2 is dysregulated.

项目总结