MicroRNAs targeting the SARS-CoV-2 entry receptor ACE2 in cardiomyocytes

The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million cases were reported by 24th July 2020. Angiotensin-converting enzyme 2 (ACE2) is a COVID-19 entry receptor regulating host cell infection. A...

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Published inJournal of molecular and cellular cardiology Vol. 148; pp. 46 - 49
Main Authors Lu, Dongchao, Chatterjee, Shambhabi, Xiao, Ke, Riedel, Isabelle, Wang, Yibin, Foo, Roger, Bär, Christian, Thum, Thomas
Format Journal Article
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Published England Elsevier Ltd 01.11.2020
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Abstract The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million cases were reported by 24th July 2020. Angiotensin-converting enzyme 2 (ACE2) is a COVID-19 entry receptor regulating host cell infection. A recent study reported that ACE2 is expressed in cardiomyocytes. In this study, we aimed to explore if there are microRNA (miRNA) molecules which target ACE2 and which may be exploited to regulate the SARS-CoV-2 receptor. Our data reveal that both Ace2 mRNA and Ace2 protein levels are inhibited by miR-200c in rat primary cardiomyocytes and importantly, in human iPSC-derived cardiomyocytes. We report the first miRNA candidate that can target ACE2 in cardiomyocytes and thus may be exploited as a preventive strategy to treat cardiovascular complications of COVID-19. •ACE2 is expressed in various cardiovascular cells including cardiomyocytes.•MicroRNA molecules can play an important role in ACE2 regulation.•MiR-200c can modulate ACE2 expression in both rat and human cardiomyocytes.
AbstractList The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million cases were reported by 24th July 2020. Angiotensin-converting enzyme 2 (ACE2) is a COVID-19 entry receptor regulating host cell infection. A recent study reported that ACE2 is expressed in cardiomyocytes. In this study, we aimed to explore if there are microRNA (miRNA) molecules which target ACE2 and which may be exploited to regulate the SARS-CoV-2 receptor. Our data reveal that both Ace2 mRNA and Ace2 protein levels are inhibited by miR-200c in rat primary cardiomyocytes and importantly, in human iPSC-derived cardiomyocytes. We report the first miRNA candidate that can target ACE2 in cardiomyocytes and thus may be exploited as a preventive strategy to treat cardiovascular complications of COVID-19.The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million cases were reported by 24th July 2020. Angiotensin-converting enzyme 2 (ACE2) is a COVID-19 entry receptor regulating host cell infection. A recent study reported that ACE2 is expressed in cardiomyocytes. In this study, we aimed to explore if there are microRNA (miRNA) molecules which target ACE2 and which may be exploited to regulate the SARS-CoV-2 receptor. Our data reveal that both Ace2 mRNA and Ace2 protein levels are inhibited by miR-200c in rat primary cardiomyocytes and importantly, in human iPSC-derived cardiomyocytes. We report the first miRNA candidate that can target ACE2 in cardiomyocytes and thus may be exploited as a preventive strategy to treat cardiovascular complications of COVID-19.
The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million cases were reported by 24th July 2020. Angiotensin-converting enzyme 2 (ACE2) is a COVID-19 entry receptor regulating host cell infection. A recent study reported that ACE2 is expressed in cardiomyocytes. In this study, we aimed to explore if there are microRNA (miRNA) molecules which target ACE2 and which may be exploited to regulate the SARS-CoV-2 receptor. Our data reveal that both Ace2 mRNA and Ace2 protein levels are inhibited by miR-200c in rat primary cardiomyocytes and importantly, in human iPSC-derived cardiomyocytes. We report the first miRNA candidate that can target ACE2 in cardiomyocytes and thus may be exploited as a preventive strategy to treat cardiovascular complications of COVID-19. •ACE2 is expressed in various cardiovascular cells including cardiomyocytes.•MicroRNA molecules can play an important role in ACE2 regulation.•MiR-200c can modulate ACE2 expression in both rat and human cardiomyocytes.
The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million cases were reported by 24th July 2020. Angiotensin-converting enzyme 2 (ACE2) is a COVID-19 entry receptor regulating host cell infection. A recent study reported that ACE2 is expressed in cardiomyocytes. In this study, we aimed to explore if there are microRNA (miRNA) molecules which target ACE2 and which may be exploited to regulate the SARS-CoV-2 receptor. Our data reveal that both Ace2 mRNA and Ace2 protein levels are inhibited by miR-200c in rat primary cardiomyocytes and importantly, in human iPSC-derived cardiomyocytes. We report the first miRNA candidate that can target ACE2 in cardiomyocytes and thus may be exploited as a preventive strategy to treat cardiovascular complications of COVID-19. • ACE2 is expressed in various cardiovascular cells including cardiomyocytes. • MicroRNA molecules can play an important role in ACE2 regulation. • MiR-200c can modulate ACE2 expression in both rat and human cardiomyocytes.
The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million cases were reported by 24th July 2020. Angiotensin-converting enzyme 2 (ACE2) is a COVID-19 entry receptor regulating host cell infection. A recent study reported that ACE2 is expressed in cardiomyocytes. In this study, we aimed to explore if there are microRNA (miRNA) molecules which target ACE2 and which may be exploited to regulate the SARS-CoV-2 receptor. Our data reveal that both Ace2 mRNA and Ace2 protein levels are inhibited by miR-200c in rat primary cardiomyocytes and importantly, in human iPSC-derived cardiomyocytes. We report the first miRNA candidate that can target ACE2 in cardiomyocytes and thus may be exploited as a preventive strategy to treat cardiovascular complications of COVID-19.
Author Xiao, Ke
Wang, Yibin
Thum, Thomas
Foo, Roger
Lu, Dongchao
Bär, Christian
Chatterjee, Shambhabi
Riedel, Isabelle
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Keywords COVID-19
ACE2
Cardiomyocytes
miRNAs
Language English
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Snippet The World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) as a public health emergency of international concern as more than 15 million...
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StartPage 46
SubjectTerms ACE2
Angiotensin-Converting Enzyme 2 - genetics
Animals
Cardiomyocytes
Cells, Cultured
Computer Simulation
COVID-19
COVID-19 - genetics
COVID-19 - virology
Fibroblasts - metabolism
Human Umbilical Vein Endothelial Cells
Humans
Induced Pluripotent Stem Cells - cytology
Mice
MicroRNAs - genetics
miRNAs
Myocardium - metabolism
Myocytes, Cardiac - metabolism
Myocytes, Cardiac - virology
Rats
Real-Time Polymerase Chain Reaction
SARS-CoV-2
Short Communication
Title MicroRNAs targeting the SARS-CoV-2 entry receptor ACE2 in cardiomyocytes
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0022282820302741
https://dx.doi.org/10.1016/j.yjmcc.2020.08.017
https://www.ncbi.nlm.nih.gov/pubmed/32891636
https://www.proquest.com/docview/2440667261
https://pubmed.ncbi.nlm.nih.gov/PMC7470794
Volume 148
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