Song Jaewon, Chow Ryan D, Pena-Hernandez Mario, Zhang Li, Loeb Skylar A, So Eui-Young, Liang Olin D, Wilen Craig B, Lee Sanghyun
Department of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University, Providence, Rhode Island, USA.
Department of Genetics, Yale School of Medicine, New Haven, Connecticut, USA.
bioRxiv. 2021 Nov 24:2021.11.23.469714. doi: 10.1101/2021.11.23.469714.
SARS-CoV-2 infection is mediated by the entry receptor ACE2. Although attachment factors and co-receptors facilitating entry are extensively studied, cellular entry factors inhibiting viral entry are largely unknown. Using a ome CRISPR activation screen, we identified human LRRC15 as an inhibitory receptor for SARS-CoV-2 entry. LRRC15 directly binds to the receptor-binding domain (RBD) of spike protein with a moderate affinity and inhibits spike-mediated entry. Analysis of human lung single cell RNA sequencing dataset reveals that expression of LRRC15 is primarily detected in fibroblasts and particularly enriched in pathological fibroblasts in COVID-19 patients. and are not co-expressed in the same cell types in the lung. Strikingly, expression of LRRC15 in ACE2-negative cells blocks spike-mediated viral entry in ACE2+ cell , suggesting a protective role of LRRC15 in a physiological context. Therefore, LRRC15 represents an inhibitory receptor for SARS-CoV-2 regulating viral entry .
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染是由进入受体血管紧张素转换酶2(ACE2)介导的。尽管促进病毒进入的附着因子和共受体已得到广泛研究,但抑制病毒进入的细胞进入因子却 largely unknown。通过全基因组CRISPR激活筛选,我们确定人类富含亮氨酸重复序列15(LRRC15)是SARS-CoV-2进入的抑制性受体。LRRC15以中等亲和力直接结合刺突蛋白的受体结合域(RBD),并抑制刺突介导的进入。对人肺单细胞RNA测序数据集的分析表明,LRRC15的表达主要在成纤维细胞中检测到,在新冠肺炎患者的病理成纤维细胞中尤其富集。LRRC15和ACE2在肺中的相同细胞类型中不共表达。引人注目的是,LRRC15在ACE2阴性细胞中的表达可阻断刺突介导的病毒在ACE2阳性细胞中的进入,这表明LRRC15在生理环境中具有保护作用。因此,LRRC15是一种调节病毒进入的SARS-CoV-2抑制性受体。