Deng Qu, Rasool Reyaz Ur, Russell Ronnie M, Natesan Ramakrishnan, Asangani Irfan A
Department of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, 421 Curie Boulevard, BRBII/III, Philadelphia, PA 19104, USA.
Department of Microbiology, University of Pennsylvania, 421 Curie Boulevard, BRBII/III, Philadelphia, PA 19104, USA.
iScience. 2021 Mar 19;24(3):102254. doi: 10.1016/j.isci.2021.102254. Epub 2021 Mar 1.
Epidemiological data showing increased severity and mortality of COVID-19 in men suggests a potential role for androgen in SARS-CoV-2 infection. Here, we present evidence for the transcriptional regulation of SARS-CoV-2 host cell receptor ACE2 and TMPRSS2 by androgen in mouse and human cells. Additionally, we demonstrate the endogenous interaction between TMPRSS2 and ACE2 in human cells and validate ACE2 as a TMPRSS2 substrate. Furthermore, camostat-a TMPRSS2 inhibitor-blocked the cleavage of pseudotype SARS-CoV-2 surface Spike without disrupting TMPRSS2-ACE2 interaction, thus providing evidence for the first time of a direct role of TMPRSS2 in priming the SARS-CoV-2 Spike, required for viral fusion to the host cell. Importantly, androgen-deprivation, anti-androgens, or camostat attenuated the SARS-CoV-2 S-mediated cellular entry. Together, our data provide a strong rationale for clinical evaluations of TMPRSS2 inhibitors and androgen-deprivation therapy/androgen receptor antagonists alone or in combination with antiviral drugs as early as clinically possible to prevent COVID-19 progression.
流行病学数据显示,男性感染新冠病毒(COVID-19)后的病情严重程度和死亡率更高,这表明雄激素在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染中可能发挥作用。在此,我们提供证据表明,雄激素在小鼠和人类细胞中对SARS-CoV-2宿主细胞受体血管紧张素转换酶2(ACE2)和跨膜丝氨酸蛋白酶2(TMPRSS2)具有转录调控作用。此外,我们证明了人类细胞中TMPRSS2与ACE2之间存在内源性相互作用,并验证了ACE2是TMPRSS2的底物。此外,TMPRSS2抑制剂抑肽酶可阻断假型SARS-CoV-2表面刺突蛋白的裂解,而不破坏TMPRSS2与ACE2的相互作用,从而首次为TMPRSS2在引发SARS-CoV-2刺突蛋白(病毒与宿主细胞融合所必需)中发挥直接作用提供了证据。重要的是,雄激素剥夺、抗雄激素药物或抑肽酶可减弱SARS-CoV-2 S介导的细胞进入。总之,我们的数据为尽早在临床上单独或联合抗病毒药物对TMPRSS2抑制剂和雄激素剥夺疗法/雄激素受体拮抗剂进行临床评估以预防COVID-19进展提供了有力依据。