Literature DB >> 33789143

Advances in use of mouse models to study the renin-angiotensin system.

Jacqueline M Emathinger1, Jonathan W Nelson2, Susan B Gurley3.   

Abstract

The renin-angiotensin system (RAS) is a highly complex hormonal cascade that spans multiple organs and cell types to regulate solute and fluid balance along with cardiovascular function. Much of our current understanding of the functions of the RAS has emerged from a series of key studies in genetically-modified animals. Here, we review key findings from ground-breaking transgenic models, spanning decades of research into the RAS, with a focus on their use in studying blood pressure. We review the physiological importance of this regulatory system as evident through the examination of mouse models for several major RAS components: angiotensinogen, renin, ACE, ACE2, and the type 1 A angiotensin receptor. Both whole-animal and cell-specific knockout models have permitted critical RAS functions to be defined and demonstrate how redundancy and multiplicity within the RAS allow for compensatory adjustments to maintain homeostasis. Moreover, these models present exciting opportunities for continued discovery surrounding the role of the RAS in disease pathogenesis and treatment for cardiovascular disease and beyond.
Copyright © 2021 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ACE; ACE2; AT1R; Cell-specific knockout mice; Mouse models

Mesh:

Substances:

Year:  2021        PMID: 33789143      PMCID: PMC9119406          DOI: 10.1016/j.mce.2021.111255

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.369


  127 in total

1.  Renal proximal tubule angiotensin AT1A receptors regulate blood pressure.

Authors:  Huiping Li; Eric T Weatherford; Deborah R Davis; Henry L Keen; Justin L Grobe; Alan Daugherty; Lisa A Cassis; Andrew M Allen; Curt D Sigmund
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-07-13       Impact factor: 3.619

2.  Collecting duct-specific knockout of renin attenuates angiotensin II-induced hypertension.

Authors:  Nirupama Ramkumar; Deborah Stuart; Sara Rees; Alfred Van Hoek; Curt D Sigmund; Donald E Kohan
Journal:  Am J Physiol Renal Physiol       Date:  2014-08-13

3.  Targeted gene duplication and disruption for analyzing quantitative genetic traits in mice.

Authors:  O Smithies; H S Kim
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-26       Impact factor: 11.205

4.  Stimulation of angiotensin type 1A receptors on catecholaminergic cells contributes to angiotensin-dependent hypertension.

Authors:  Nikola Jancovski; Jaspreet K Bassi; David A Carter; Yan-Ting Choong; Angela Connelly; Thu-Phuc Nguyen; Daian Chen; Elena V Lukoshkova; Clement Menuet; Geoffrey A Head; Andrew M Allen
Journal:  Hypertension       Date:  2013-09-03       Impact factor: 10.190

5.  Nephrogenesis and renovascular development in angiotensinogen-deficient mice.

Authors:  M Nagata; K Tanimoto; A Fukamizu; Y Kon; F Sugiyama; K Yagami; K Murakami; T Watanabe
Journal:  Lab Invest       Date:  1996-11       Impact factor: 5.662

6.  Effects on blood pressure and exploratory behaviour of mice lacking angiotensin II type-2 receptor.

Authors:  T Ichiki; P A Labosky; C Shiota; S Okuyama; Y Imagawa; A Fogo; F Niimura; I Ichikawa; B L Hogan; T Inagami
Journal:  Nature       Date:  1995-10-26       Impact factor: 49.962

Review 7.  Novel angiotensin peptides regulate blood pressure, endothelial function, and natriuresis.

Authors:  C M Ferrario; M C Chappell; R H Dean; S N Iyer
Journal:  J Am Soc Nephrol       Date:  1998-09       Impact factor: 10.121

8.  Cardiac phenotype and angiotensin II levels in AT1a, AT1b, and AT2 receptor single, double, and triple knockouts.

Authors:  Joep H M van Esch; Florian Gembardt; Anja Sterner-Kock; Silvia Heringer-Walther; Thu H Le; Dirk Lassner; Theo Stijnen; Thomas M Coffman; Heinz-Peter Schultheiss; A H Jan Danser; Thomas Walther
Journal:  Cardiovasc Res       Date:  2010-01-12       Impact factor: 10.787

9.  The Absence of the ACE N-Domain Decreases Renal Inflammation and Facilitates Sodium Excretion during Diabetic Kidney Disease.

Authors:  Masahiro Eriguchi; Ellen A Bernstein; Luciana C Veiras; Zakir Khan; Duo Yao Cao; Sebastien Fuchs; Alicia A McDonough; Jorge E Toblli; Romer A Gonzalez-Villalobos; Kenneth E Bernstein; Jorge F Giani
Journal:  J Am Soc Nephrol       Date:  2018-09-05       Impact factor: 10.121

10.  Genetic Deletion of ACE2 Induces Vascular Dysfunction in C57BL/6 Mice: Role of Nitric Oxide Imbalance and Oxidative Stress.

Authors:  Luiza A Rabelo; Mihail Todiras; Valéria Nunes-Souza; Fatimunnisa Qadri; István András Szijártó; Maik Gollasch; Josef M Penninger; Michael Bader; Robson A Santos; Natalia Alenina
Journal:  PLoS One       Date:  2016-04-12       Impact factor: 3.240

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