SARS-CoV-2 hijacks macropinocytosis to facilitate its entry and promote viral spike-mediated cell-to-cell fusion

文献类型： 外文期刊

第一作者： Zhang, Yu-Yuan

作者： Zhang, Yu-Yuan;Wang, Shu-Jie;Wang, Tong-Yun;Chen, Meng;Liu, Jianbo;Na, Lei;Yang, Yue-Lin;Yang, Yong-Bo;Yin, Xin;Cai, Xue-Hui;Tang, Yan-Dong;Liang, Ronghui;Ye, Zi-Wei;Yuan, Shuofeng;Yuan, Shuofeng

作者机构：

期刊名称：JOURNAL OF BIOLOGICAL CHEMISTRY （ 影响因子：5.486； 五年影响因子：5.295 ）

ISSN：

年卷期： 2022 年 298 卷 11 期

页码：

收录情况： SCI

摘要： Revealing the mechanisms of severe acute respiratory syn-drome coronavirus 2 (SARS-CoV-2) entry and cell-to-cell spread might provide insights for understanding the underly-ing mechanisms of viral pathogenesis, tropism, and virulence. The signaling pathways involved in SARS-CoV-2 entry and viral spike-mediated cell-to-cell fusion remain elusive. In the current study, we found that macropinocytosis inhibitors significantly suppressed SARS-CoV-2 infection at both the entry and viral spike-mediated cell-to-cell fusion steps. We demonstrated that SARS-CoV-2 entry required the small GTPase Rac1 and its effector kinase p21-activated kinase 1 by dominant-negative and RNAi assays in human embryonic kidney 293T-angiotensin-converting enzyme 2 cells and that the serine protease transmembrane serine protease 2 reversed the decrease in SARS-CoV-2 entry caused by the macro-pinocytosis inhibitors. Moreover, in the cell-to-cell fusion assay, we confirmed that macropinocytosis inhibitors signifi- cantly decreased viral spike-mediated cell-to-cell fusion. Overall, we provided evidence that SARS-CoV-2 utilizes a macropinocytosis pathway to enter target cells and to effi- ciently promote viral spike-mediated cell-to-cell fusion.

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