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      Stem-cell-derived trophoblast organoids model human placental development and susceptibility to emerging pathogens.

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          Abstract

          Trophoblast organoids derived from placental villi provide a 3D model system of human placental development, but access to first-trimester tissues is limited. Here, we report that trophoblast stem cells isolated from naive human pluripotent stem cells (hPSCs) can efficiently self-organize into 3D stem-cell-derived trophoblast organoids (SC-TOs) with a villous architecture similar to primary trophoblast organoids. Single-cell transcriptome analysis reveals the presence of distinct cytotrophoblast and syncytiotrophoblast clusters and a small cluster of extravillous trophoblasts, which closely correspond to trophoblast identities in the post-implantation embryo. These organoid cultures display clonal X chromosome inactivation patterns previously described in the human placenta. We further demonstrate that SC-TOs exhibit selective vulnerability to emerging pathogens (SARS-CoV-2 and Zika virus), which correlates with expression levels of their respective entry factors. The generation of trophoblast organoids from naive hPSCs provides an accessible 3D model system of the developing placenta and its susceptibility to emerging pathogens.

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          Author and article information

          Journal
          Cell Stem Cell
          Cell stem cell
          Elsevier BV
          1875-9777
          1875-9777
          May 05 2022
          : 29
          : 5
          Affiliations
          [1 ] Department of Developmental Biology and Center of Regenerative Medicine, Washington University School of Medicine, 4515 McKinley Ave, Room 3313, St. Louis, MO 63110, USA.
          [2 ] Department of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA.
          [3 ] Division of Dermatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
          [4 ] Division of Gastroenterology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
          [5 ] Division of Infection Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
          [6 ] Department of Developmental Biology and Center of Regenerative Medicine, Washington University School of Medicine, 4515 McKinley Ave, Room 3313, St. Louis, MO 63110, USA; Division of Nephrology and Institute for Informatics (I(2)), Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: s.dietmann@wustl.edu.
          [7 ] Department of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA. Electronic address: indira.mysorekar@bcm.edu.
          [8 ] Department of Developmental Biology and Center of Regenerative Medicine, Washington University School of Medicine, 4515 McKinley Ave, Room 3313, St. Louis, MO 63110, USA. Electronic address: t.theunissen@wustl.edu.
          Article
          S1934-5909(22)00157-6 NIHMS1804351
          10.1016/j.stem.2022.04.004
          9136997
          35523141
          c7c2864a-a3de-41eb-89b4-ce45124f359c
          History

          naive pluripotency,placental development,single-cell transcriptomics,syncytiotrophoblast,trophoblast organoids,trophoblast stem cells,SARS-CoV-2,X chromosome inactivation,Zika virus,cytotrophoblast,extravillous trophoblast

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