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Does the human placenta express the canonical cell entry mediators for SARS-CoV-2?
Pique-Regi, Roger; Romero, Roberto; Tarca, Adi L; Luca, Francesca; Xu, Yi; Alazizi, Adnan; Leng, Yaozhu; Hsu, Chaur-Dong; Gomez-Lopez, Nardhy.
Afiliación
  • Pique-Regi R; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, <italic>Eunice Kennedy Shriver</italic> National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services
  • Romero R; Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, United States.
  • Tarca AL; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, United States.
  • Luca F; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, <italic>Eunice Kennedy Shriver</italic> National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services
  • Xu Y; Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, United States.
  • Alazizi A; Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, United States.
  • Leng Y; Department of Epidemiology and Biostatistics, Michigan State University, East Lansing, United States.
  • Hsu CD; Detroit Medical Center, Detroit, United States.
  • Gomez-Lopez N; Department of Obstetrics and Gynecology, Florida International University, Miami, United States.
Elife ; 92020 07 14.
Article en En | MEDLINE | ID: mdl-32662421
ABSTRACT
The pandemic of coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has affected more than 10 million people, including pregnant women. To date, no consistent evidence for the vertical transmission of SARS-CoV-2 exists. The novel coronavirus canonically utilizes the angiotensin-converting enzyme 2 (ACE2) receptor and the serine protease TMPRSS2 for cell entry. Herein, building upon our previous single-cell study (Pique-Regi et al., 2019), another study, and new single-cell/nuclei RNA-sequencing data, we investigated the expression of ACE2 and TMPRSS2 throughout pregnancy in the placenta as well as in third-trimester chorioamniotic membranes. We report that co-transcription of ACE2 and TMPRSS2 is negligible in the placenta, thus not a likely path of vertical transmission for SARS-CoV-2. By contrast, receptors for Zika virus and cytomegalovirus, which cause congenital infections, are highly expressed by placental cell types. These data show that the placenta minimally expresses the canonical cell-entry mediators for SARS-CoV-2.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Placenta / Neumonía Viral / Receptores Virales / Serina Endopeptidasas / Infecciones por Coronavirus / Internalización del Virus / Betacoronavirus Límite: Female / Humans / Pregnancy Idioma: En Revista: Elife Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Placenta / Neumonía Viral / Receptores Virales / Serina Endopeptidasas / Infecciones por Coronavirus / Internalización del Virus / Betacoronavirus Límite: Female / Humans / Pregnancy Idioma: En Revista: Elife Año: 2020 Tipo del documento: Article
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