| Literature DB >> 33774649 |
Miao-Miao Zhao1, Wei-Li Yang1, Fang-Yuan Yang1, Li Zhang2, Wei-Jin Huang2, Wei Hou3, Chang-Fa Fan4, Rong-Hua Jin3, Ying-Mei Feng5, You-Chun Wang6, Jin-Kui Yang7.
Abstract
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.Entities:
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Year: 2021 PMID: 33774649 PMCID: PMC7997800 DOI: 10.1038/s41392-021-00558-8
Source DB: PubMed Journal: Signal Transduct Target Ther ISSN: 2059-3635