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 in | Journal of molecular and cellular cardiology Vol. 148; pp. 46 - 49 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Dongchao surname: Lu fullname: Lu, Dongchao organization: Institute of Molecular and Translational Therapeutic Strategies, Hannover Medical School, Hannover, Germany – sequence: 2 givenname: Shambhabi surname: Chatterjee fullname: Chatterjee, Shambhabi organization: Institute of Molecular and Translational Therapeutic Strategies, Hannover Medical School, Hannover, Germany – sequence: 3 givenname: Ke surname: Xiao fullname: Xiao, Ke organization: Institute of Molecular and Translational Therapeutic Strategies, Hannover Medical School, Hannover, Germany – sequence: 4 givenname: Isabelle surname: Riedel fullname: Riedel, Isabelle organization: Institute of Molecular and Translational Therapeutic Strategies, Hannover Medical School, Hannover, Germany – sequence: 5 givenname: Yibin surname: Wang fullname: Wang, Yibin organization: Department of Anesthesiology, Medicine and Physiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA, USA – sequence: 6 givenname: Roger surname: Foo fullname: Foo, Roger organization: Genome Institute of Singapore, Cardiovascular Research Institute, National University of Singapore, Centre for Translational Medicine, Singapore, Republic of Singapore – sequence: 7 givenname: Christian surname: Bär fullname: Bär, Christian email: baer.christian@mh-hannover.de organization: Institute of Molecular and Translational Therapeutic Strategies, Hannover Medical School, Hannover, Germany – sequence: 8 givenname: Thomas surname: Thum fullname: Thum, Thomas email: thum.thomas@mh-hannover.de organization: Institute of Molecular and Translational Therapeutic Strategies, Hannover Medical School, Hannover, Germany |
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Keywords | COVID-19 ACE2 Cardiomyocytes miRNAs |
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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 |
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