Zhao Miao-Miao, Yang Wei-Li, Yang Fang-Yuan, Zhang Li, Huang Wei-Jin, Hou Wei, Fan Chang-Fa, Jin Rong-Hua, Feng Ying-Mei, Wang You-Chun, Yang Jin-Kui
Department of Endocrinology, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Division of HIV/AIDS and Sex-Transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, China.
Signal Transduct Target Ther. 2021 Mar 27;6(1):134. doi: 10.1038/s41392-021-00558-8.
To discover new drugs to combat COVID-19, an understanding of the molecular basis of SARS-CoV-2 infection is urgently needed. Here, for the first time, we report the crucial role of cathepsin L (CTSL) in patients with COVID-19. The circulating level of CTSL was elevated after SARS-CoV-2 infection and was positively correlated with disease course and severity. Correspondingly, SARS-CoV-2 pseudovirus infection increased CTSL expression in human cells in vitro and human ACE2 transgenic mice in vivo, while CTSL overexpression, in turn, enhanced pseudovirus infection in human cells. CTSL functionally cleaved the SARS-CoV-2 spike protein and enhanced virus entry, as evidenced by CTSL overexpression and knockdown in vitro and application of CTSL inhibitor drugs in vivo. Furthermore, amantadine, a licensed anti-influenza drug, significantly inhibited CTSL activity after SARS-CoV-2 pseudovirus infection and prevented infection both in vitro and in vivo. Therefore, CTSL is a promising target for new anti-COVID-19 drug development.
为了发现抗击新型冠状病毒肺炎(COVID-19)的新药,迫切需要了解严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的分子基础。在此,我们首次报道了组织蛋白酶L(CTSL)在COVID-19患者中的关键作用。SARS-CoV-2感染后,CTSL的循环水平升高,且与病程和严重程度呈正相关。相应地,SARS-CoV-2假病毒感染在体外人细胞和体内人血管紧张素转换酶2(ACE2)转基因小鼠中增加了CTSL的表达,而CTSL的过表达反过来又增强了人细胞中的假病毒感染。CTSL在功能上切割了SARS-CoV-2刺突蛋白并增强了病毒进入,体外CTSL过表达和敲低以及体内应用CTSL抑制剂药物证明了这一点。此外,金刚烷胺是一种已获许可的抗流感药物,在SARS-CoV-2假病毒感染后能显著抑制CTSL活性,并在体外和体内预防感染。因此,CTSL是新型抗COVID-19药物开发的一个有前景的靶点。