ACE2: a key modulator of the renin-angiotensin system and pregnancy
Angiotensin-converting enzyme 2 (ACE2) is a membrane-bound protein containing 805 amino acids. ACE2 shows approximately 42% sequence similarity to somatic ACE but has different biochemical activities. The key role of ACE2 is to catalyze the vasoconstrictor peptide angiotensin (ANG) II to Ang-(1-7),...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2021-12, Vol.321 (6), p.R833-R843 |
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creator | Tamanna, Sonia Lumbers, Eugenie R Morosin, Saije K Delforce, Sarah J Pringle, Kirsty G |
description | Angiotensin-converting enzyme 2 (ACE2) is a membrane-bound protein containing 805 amino acids. ACE2 shows approximately 42% sequence similarity to somatic ACE but has different biochemical activities. The key role of ACE2 is to catalyze the vasoconstrictor peptide angiotensin (ANG) II to Ang-(1-7), thus regulating the two major counterbalancing pathways of the renin-angiotensin system (RAS). In this way, ACE2 plays a protective role in end-organ damage by protecting tissues from the proinflammatory actions of ANG II. The circulating RAS is activated in normal pregnancy and is essential for maintaining fluid and electrolyte homeostasis and blood pressure. Renin-angiotensin systems are also found in the conceptus. In this review, we summarize the current knowledge on the regulation and function of circulating and uteroplacental ACE2 in uncomplicated and complicated pregnancies, including those affected by preeclampsia and fetal growth restriction. Since ACE2 is the receptor for SARS-CoV-2, and COVID-19 in pregnancy is associated with more severe disease and increased risk of abnormal pregnancy outcomes, we also discuss the role of ACE2 in mediating some of these adverse consequences. We propose that dysregulation of ACE2 plays a critical role in the development of preeclampsia, fetal growth restriction, and COVID-19-associated pregnancy pathologies and suggest that human recombinant soluble ACE2 could be a novel therapeutic to treat and/or prevent these pregnancy complications. |
doi_str_mv | 10.1152/ajpregu.00211.2021 |
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ACE2 shows approximately 42% sequence similarity to somatic ACE but has different biochemical activities. The key role of ACE2 is to catalyze the vasoconstrictor peptide angiotensin (ANG) II to Ang-(1-7), thus regulating the two major counterbalancing pathways of the renin-angiotensin system (RAS). In this way, ACE2 plays a protective role in end-organ damage by protecting tissues from the proinflammatory actions of ANG II. The circulating RAS is activated in normal pregnancy and is essential for maintaining fluid and electrolyte homeostasis and blood pressure. Renin-angiotensin systems are also found in the conceptus. In this review, we summarize the current knowledge on the regulation and function of circulating and uteroplacental ACE2 in uncomplicated and complicated pregnancies, including those affected by preeclampsia and fetal growth restriction. Since ACE2 is the receptor for SARS-CoV-2, and COVID-19 in pregnancy is associated with more severe disease and increased risk of abnormal pregnancy outcomes, we also discuss the role of ACE2 in mediating some of these adverse consequences. We propose that dysregulation of ACE2 plays a critical role in the development of preeclampsia, fetal growth restriction, and COVID-19-associated pregnancy pathologies and suggest that human recombinant soluble ACE2 could be a novel therapeutic to treat and/or prevent these pregnancy complications.</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00211.2021</identifier><identifier>PMID: 34668428</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>ACE2 ; Amino acids ; Angiotensin ; Angiotensin II ; Angiotensin-converting enzyme 2 ; Angiotensin-Converting Enzyme 2 - metabolism ; Angiotensin-Converting Enzyme 2 - therapeutic use ; Animals ; Blood Pressure ; Complications ; Coronaviruses ; COVID-19 ; COVID-19 - enzymology ; COVID-19 - physiopathology ; COVID-19 - virology ; Endocrine system ; Female ; Fetal Growth Retardation - enzymology ; Fetal Growth Retardation - physiopathology ; Fetuses ; Health risks ; Homeostasis ; Humans ; Inflammation ; Inflammation Mediators - metabolism ; Membrane proteins ; Peptidyl-dipeptidase A ; Placenta - enzymology ; Placenta - physiopathology ; Pre-eclampsia ; Pre-Eclampsia - enzymology ; Pre-Eclampsia - physiopathology ; Preeclampsia ; Pregnancy ; Pregnancy complications ; Pregnancy Complications - drug therapy ; Pregnancy Complications - enzymology ; Pregnancy Complications - physiopathology ; Pregnancy Complications, Infectious - enzymology ; Pregnancy Complications, Infectious - physiopathology ; Pregnancy Complications, Infectious - virology ; Renin ; Renin-Angiotensin System ; Review ; SARS-CoV-2 - pathogenicity ; Severe acute respiratory syndrome coronavirus 2 ; Uterus - enzymology ; Uterus - physiopathology ; Water-Electrolyte Balance</subject><ispartof>American journal of physiology. 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Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>Angiotensin-converting enzyme 2 (ACE2) is a membrane-bound protein containing 805 amino acids. ACE2 shows approximately 42% sequence similarity to somatic ACE but has different biochemical activities. The key role of ACE2 is to catalyze the vasoconstrictor peptide angiotensin (ANG) II to Ang-(1-7), thus regulating the two major counterbalancing pathways of the renin-angiotensin system (RAS). In this way, ACE2 plays a protective role in end-organ damage by protecting tissues from the proinflammatory actions of ANG II. The circulating RAS is activated in normal pregnancy and is essential for maintaining fluid and electrolyte homeostasis and blood pressure. Renin-angiotensin systems are also found in the conceptus. In this review, we summarize the current knowledge on the regulation and function of circulating and uteroplacental ACE2 in uncomplicated and complicated pregnancies, including those affected by preeclampsia and fetal growth restriction. Since ACE2 is the receptor for SARS-CoV-2, and COVID-19 in pregnancy is associated with more severe disease and increased risk of abnormal pregnancy outcomes, we also discuss the role of ACE2 in mediating some of these adverse consequences. We propose that dysregulation of ACE2 plays a critical role in the development of preeclampsia, fetal growth restriction, and COVID-19-associated pregnancy pathologies and suggest that human recombinant soluble ACE2 could be a novel therapeutic to treat and/or prevent these pregnancy complications.</description><subject>ACE2</subject><subject>Amino acids</subject><subject>Angiotensin</subject><subject>Angiotensin II</subject><subject>Angiotensin-converting enzyme 2</subject><subject>Angiotensin-Converting Enzyme 2 - metabolism</subject><subject>Angiotensin-Converting Enzyme 2 - therapeutic use</subject><subject>Animals</subject><subject>Blood Pressure</subject><subject>Complications</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - enzymology</subject><subject>COVID-19 - physiopathology</subject><subject>COVID-19 - virology</subject><subject>Endocrine system</subject><subject>Female</subject><subject>Fetal Growth Retardation - enzymology</subject><subject>Fetal Growth Retardation - physiopathology</subject><subject>Fetuses</subject><subject>Health risks</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Inflammation Mediators - metabolism</subject><subject>Membrane proteins</subject><subject>Peptidyl-dipeptidase A</subject><subject>Placenta - enzymology</subject><subject>Placenta - physiopathology</subject><subject>Pre-eclampsia</subject><subject>Pre-Eclampsia - enzymology</subject><subject>Pre-Eclampsia - physiopathology</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>Pregnancy complications</subject><subject>Pregnancy Complications - drug therapy</subject><subject>Pregnancy Complications - enzymology</subject><subject>Pregnancy Complications - physiopathology</subject><subject>Pregnancy Complications, Infectious - enzymology</subject><subject>Pregnancy Complications, Infectious - physiopathology</subject><subject>Pregnancy Complications, Infectious - virology</subject><subject>Renin</subject><subject>Renin-Angiotensin System</subject><subject>Review</subject><subject>SARS-CoV-2 - pathogenicity</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Uterus - enzymology</subject><subject>Uterus - physiopathology</subject><subject>Water-Electrolyte Balance</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUtP6zAQhS10EZTHH2CBLN0Nm5QZ23EcFkio4iUhsYG15aR2SUnsYidX6r-_KRQEbGYWc-bMHH2EnCBMEXN2bparaBfDFIAhTtlYd8hkHLAMRQl_yAS45JlELPfJQUpLABBc8D2yz4WUSjA1IbOr2TW7oIa-2jXtwnxoTR8iDY72L5ZG6xufGb9oQm99ajxN69Tbjho_p5vj3vh6fUR2nWmTPd72Q_J8c_00u8seHm_vZ1cPWS049JkpFDMc3bxijEOFRc5kCSovnXF1WTlE42xZCwdYKVU5WRaiRlcaYVFK4PyQXH74roaqs_Pa-j6aVq9i05m41sE0-ufENy96Ef5ppSQrlBgNzrYGMbwNNvW6a1Jt29Z4G4akWa4EoBQFjNK_v6TLMEQ_xtNMQs5B5JiPKvahqmNIKVr39QyC3jDSW0b6nZHeMBqXTr_H-Fr5hML_A4B9jkE</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Tamanna, Sonia</creator><creator>Lumbers, Eugenie R</creator><creator>Morosin, Saije K</creator><creator>Delforce, Sarah J</creator><creator>Pringle, Kirsty G</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6810-4226</orcidid><orcidid>https://orcid.org/0000-0003-3945-3923</orcidid><orcidid>https://orcid.org/0000-0002-6770-0496</orcidid><orcidid>https://orcid.org/0000-0001-8974-5575</orcidid></search><sort><creationdate>20211201</creationdate><title>ACE2: a key modulator of the renin-angiotensin system and pregnancy</title><author>Tamanna, Sonia ; Lumbers, Eugenie R ; Morosin, Saije K ; Delforce, Sarah J ; Pringle, Kirsty G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-a782a31fdb2230b1752690859fafc9bf11afe9c4f01b88bf6974c1f9a4e166033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>ACE2</topic><topic>Amino acids</topic><topic>Angiotensin</topic><topic>Angiotensin II</topic><topic>Angiotensin-converting enzyme 2</topic><topic>Angiotensin-Converting Enzyme 2 - metabolism</topic><topic>Angiotensin-Converting Enzyme 2 - therapeutic use</topic><topic>Animals</topic><topic>Blood Pressure</topic><topic>Complications</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - enzymology</topic><topic>COVID-19 - physiopathology</topic><topic>COVID-19 - virology</topic><topic>Endocrine system</topic><topic>Female</topic><topic>Fetal Growth Retardation - enzymology</topic><topic>Fetal Growth Retardation - physiopathology</topic><topic>Fetuses</topic><topic>Health risks</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Inflammation Mediators - metabolism</topic><topic>Membrane proteins</topic><topic>Peptidyl-dipeptidase A</topic><topic>Placenta - enzymology</topic><topic>Placenta - physiopathology</topic><topic>Pre-eclampsia</topic><topic>Pre-Eclampsia - enzymology</topic><topic>Pre-Eclampsia - physiopathology</topic><topic>Preeclampsia</topic><topic>Pregnancy</topic><topic>Pregnancy complications</topic><topic>Pregnancy Complications - drug therapy</topic><topic>Pregnancy Complications - enzymology</topic><topic>Pregnancy Complications - physiopathology</topic><topic>Pregnancy Complications, Infectious - enzymology</topic><topic>Pregnancy Complications, Infectious - physiopathology</topic><topic>Pregnancy Complications, Infectious - virology</topic><topic>Renin</topic><topic>Renin-Angiotensin System</topic><topic>Review</topic><topic>SARS-CoV-2 - pathogenicity</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Uterus - enzymology</topic><topic>Uterus - physiopathology</topic><topic>Water-Electrolyte Balance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamanna, Sonia</creatorcontrib><creatorcontrib>Lumbers, Eugenie R</creatorcontrib><creatorcontrib>Morosin, Saije K</creatorcontrib><creatorcontrib>Delforce, Sarah J</creatorcontrib><creatorcontrib>Pringle, Kirsty G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamanna, Sonia</au><au>Lumbers, Eugenie R</au><au>Morosin, Saije K</au><au>Delforce, Sarah J</au><au>Pringle, Kirsty G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ACE2: a key modulator of the renin-angiotensin system and pregnancy</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>321</volume><issue>6</issue><spage>R833</spage><epage>R843</epage><pages>R833-R843</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><abstract>Angiotensin-converting enzyme 2 (ACE2) is a membrane-bound protein containing 805 amino acids. ACE2 shows approximately 42% sequence similarity to somatic ACE but has different biochemical activities. The key role of ACE2 is to catalyze the vasoconstrictor peptide angiotensin (ANG) II to Ang-(1-7), thus regulating the two major counterbalancing pathways of the renin-angiotensin system (RAS). In this way, ACE2 plays a protective role in end-organ damage by protecting tissues from the proinflammatory actions of ANG II. The circulating RAS is activated in normal pregnancy and is essential for maintaining fluid and electrolyte homeostasis and blood pressure. Renin-angiotensin systems are also found in the conceptus. In this review, we summarize the current knowledge on the regulation and function of circulating and uteroplacental ACE2 in uncomplicated and complicated pregnancies, including those affected by preeclampsia and fetal growth restriction. Since ACE2 is the receptor for SARS-CoV-2, and COVID-19 in pregnancy is associated with more severe disease and increased risk of abnormal pregnancy outcomes, we also discuss the role of ACE2 in mediating some of these adverse consequences. We propose that dysregulation of ACE2 plays a critical role in the development of preeclampsia, fetal growth restriction, and COVID-19-associated pregnancy pathologies and suggest that human recombinant soluble ACE2 could be a novel therapeutic to treat and/or prevent these pregnancy complications.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>34668428</pmid><doi>10.1152/ajpregu.00211.2021</doi><orcidid>https://orcid.org/0000-0001-6810-4226</orcidid><orcidid>https://orcid.org/0000-0003-3945-3923</orcidid><orcidid>https://orcid.org/0000-0002-6770-0496</orcidid><orcidid>https://orcid.org/0000-0001-8974-5575</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ACE2 Amino acids Angiotensin Angiotensin II Angiotensin-converting enzyme 2 Angiotensin-Converting Enzyme 2 - metabolism Angiotensin-Converting Enzyme 2 - therapeutic use Animals Blood Pressure Complications Coronaviruses COVID-19 COVID-19 - enzymology COVID-19 - physiopathology COVID-19 - virology Endocrine system Female Fetal Growth Retardation - enzymology Fetal Growth Retardation - physiopathology Fetuses Health risks Homeostasis Humans Inflammation Inflammation Mediators - metabolism Membrane proteins Peptidyl-dipeptidase A Placenta - enzymology Placenta - physiopathology Pre-eclampsia Pre-Eclampsia - enzymology Pre-Eclampsia - physiopathology Preeclampsia Pregnancy Pregnancy complications Pregnancy Complications - drug therapy Pregnancy Complications - enzymology Pregnancy Complications - physiopathology Pregnancy Complications, Infectious - enzymology Pregnancy Complications, Infectious - physiopathology Pregnancy Complications, Infectious - virology Renin Renin-Angiotensin System Review SARS-CoV-2 - pathogenicity Severe acute respiratory syndrome coronavirus 2 Uterus - enzymology Uterus - physiopathology Water-Electrolyte Balance |
title | ACE2: a key modulator of the renin-angiotensin system and pregnancy |
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