Author: Lemes, Robertha Mariana Rodrigues; Costa, Angelica Jardim; Bartolomeo, Cynthia Silva; Bassani, Taysa Bervian; Nishino, Michelle Sayuri; Pereira, Gustavo Jose da Silva; Smaili, Soraya Soubhi; Maciel, Rui Monteiro de Barros; Braconi, Carla Torres; da Cruz, Edgar Ferreira; Ramirez, Ana Lopez; Maricatto, Juliana Terzi; Janini, Luiz Mario Ramos; Prado, Carla Máximo; Stilhano, Roberta Sessa; Ureshino, Rodrigo Portes
Title: 17βâ€estradiol reduces SARSâ€CoVâ€2 infection in vitro Cord-id: r5yavxpg Document date: 2021_1_19
ID: r5yavxpg
Snippet: The COVIDâ€19 has originated from Wuhan, China, in December 2019 and has been affecting the public health system, society, and economy in an unheardâ€of manner. There is no specific treatment or vaccine available for COVIDâ€19. Previous data showed that men are more affected than women by COVIDâ€19, then we hypothesized whether sex hormones could be protecting the female organism against the infection. VERO E6 cells have been commonly used as in vitro model for SARSâ€CoVâ€2 infection. In o
Document: The COVIDâ€19 has originated from Wuhan, China, in December 2019 and has been affecting the public health system, society, and economy in an unheardâ€of manner. There is no specific treatment or vaccine available for COVIDâ€19. Previous data showed that men are more affected than women by COVIDâ€19, then we hypothesized whether sex hormones could be protecting the female organism against the infection. VERO E6 cells have been commonly used as in vitro model for SARSâ€CoVâ€2 infection. In our experimental approach, we have treated VERO E6 cells with 17βâ€estradiol to evaluate the modulation of SARSâ€CoVâ€2 infection in this cell line. Here we demonstrated that estrogen protein receptors ERα, ERβ, and GPER1 are expressed by VERO E6 cells and could be used to study the effects of this steroid hormone. Previous and 24â€hours postâ€infection, cells treated with 17βâ€estradiol revealed a reduction in the viral load. Afterward, we found that SARSâ€CoVâ€2 infection per se results in ACE2 and TMPRSS2 increased gene expression in VERO E6â€cell, which could be generating a cycle of virus infection in host cells. The estrogen treatment reduces the levels of the TMPRSS2, which are involved with SARSâ€CoVâ€2 infectiveness capacity, and hence, reducing the pathogenicity/genesis. These data suggest that estrogen could be a potential therapeutic target promoting cell protection against SARSâ€CoVâ€2. This opens new possibilities for further studies on 17βâ€estradiol in human cell lines infected by SARSâ€CoVâ€2 and at least in part, explain why men developed a more severe COVIDâ€19 compared to women.
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