血管紧张素转化酶2
小RNA
2019年冠状病毒病(COVID-19)
受体
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019-20冠状病毒爆发
冠状病毒
信使核糖核酸
生物
下调和上调
细胞生物学
疾病
病毒学
医学
基因
内科学
生物化学
传染病(医学专业)
爆发
作者
Dongchao Lv,Shambhabi Chatterjee,Ke Xiao,Isabelle Riedel,Yibin Wang,Roger Foo,Christian Bär,Thomas Thum
标识
DOI:10.1016/j.yjmcc.2020.08.017
摘要
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.
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