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1000 Titel
  • ACE2: The key Molecule for Understanding the Pathophysiology of Severe and Critical Conditions of COVID-19: Demon or Angel?
1000 Autor/in
  1. Xiao, Li |
  2. Sakagami, Hiroshi |
  3. Miwa, Nobuhiko |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-04-28
1000 Erschienen in
1000 Quellenangabe
  • 12(5):491
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3390/v12050491 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Recently, the SARS-CoV-2 induced disease COVID-19 has spread all over the world. Nearly 20% of the patients have severe or critical conditions. SARS-CoV-2 exploits ACE2 for host cell entry. ACE2 plays an essential role in the renin–angiotensin–aldosterone system (RAAS), which regulates blood pressure and fluid balance. ACE2 also protects organs from inflammatory injuries and regulates intestinal functions. ACE2 can be shed by two proteases, ADAM17 and TMPRSS2. TMPRSS2-cleaved ACE2 allows SARS-CoV-2 cell entry, whereas ADAM17-cleaved ACE2 offers protection to organs. SARS-CoV-2 infection-caused ACE2 dysfunction worsens COVID-19 and could initiate multi-organ failure. Here, we will explain the role of ACE2 in the pathogenesis of severe and critical conditions of COVID-19 and discuss auspicious strategies for controlling the disease.
1000 Sacherschließung
gnd 1206347392 COVID-19
lokal RAAS
lokal B0AT1
lokal ACE2
lokal Ang-(1-7)
lokal TMPRSS2
lokal SARS-CoV-2
lokal ADAM17
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-3053-4930|https://orcid.org/0000-0001-8001-2121|https://frl.publisso.de/adhoc/uri/TWl3YSwgTm9idWhpa28=
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1000 Erstellt am 2020-04-28T16:21:51.345+0200
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  1. oai:frl.publisso.de:frl:6420527 |
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