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ACE2 mouse models: a toolbox for cardiovascular and pulmonary research.
Jia, Hongpeng; Yue, Xinping; Lazartigues, Eric.
  • Jia H; Division of Pediatric Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
  • Yue X; Department of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
  • Lazartigues E; Department of Pharmacology & Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA. elazar@lsuhsc.edu.
Nat Commun ; 11(1): 5165, 2020 10 14.
Article in English | MEDLINE | ID: covidwho-872694
ABSTRACT
Angiotensin-converting enzyme 2 (ACE2) has been identified as the host entry receptor for the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for the COVID-19 pandemic. ACE2 is a regulatory enzyme of the renin-angiotensin system and has protective functions in many cardiovascular, pulmonary and metabolic diseases. This review summarizes available murine models with systemic or organ-specific deletion of ACE2, or with overexpression of murine or human ACE2. The purpose of this review is to provide researchers with the genetic tools available for further understanding of ACE2 biology and for the investigation of ACE2 in the pathogenesis and treatment of COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Cardiovascular Diseases / Peptidyl-Dipeptidase A / Disease Models, Animal / Lung Diseases Limits: Animals / Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2020 Document Type: Article Affiliation country: S41467-020-18880-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Cardiovascular Diseases / Peptidyl-Dipeptidase A / Disease Models, Animal / Lung Diseases Limits: Animals / Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2020 Document Type: Article Affiliation country: S41467-020-18880-0