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In vivo development of immune tissue in human intestinal organoids transplanted into humanized mice.
Bouffi, Carine; Wikenheiser-Brokamp, Kathryn A; Chaturvedi, Praneet; Sundaram, Nambirajan; Goddard, Gillian R; Wunderlich, Mark; Brown, Nicole E; Staab, Janet F; Latanich, Rachel; Zachos, Nicholas C; Holloway, Emily M; Mahe, Maxime M; Poling, Holly M; Vales, Simon; Fisher, Garrett W; Spence, Jason R; Mulloy, James C; Zorn, Aaron M; Wells, James M; Helmrath, Michael A.
Afiliação
  • Bouffi C; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Wikenheiser-Brokamp KA; Division of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Chaturvedi P; Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH, USA.
  • Sundaram N; Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Goddard GR; Center for Stem Cell and Organoid Medicine (CuSTOM), Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Wunderlich M; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Brown NE; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Staab JF; Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Latanich R; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Zachos NC; Division of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Holloway EM; Division of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Mahe MM; Division of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Poling HM; Université de Nantes, Inserm, TENS, The Enteric Nervous System in Gut and Brain Diseases, IMAD, Nantes, France.
  • Vales S; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Fisher GW; Université de Nantes, Inserm, TENS, The Enteric Nervous System in Gut and Brain Diseases, IMAD, Nantes, France.
  • Spence JR; Department of Pediatrics, University of Cincinnati, Cincinnati, OH, USA.
  • Mulloy JC; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Zorn AM; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Wells JM; Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Helmrath MA; Division of Gastroenterology, Department of Internal Medicine, Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Nat Biotechnol ; 41(6): 824-831, 2023 06.
Article em En | MEDLINE | ID: mdl-36702898
ABSTRACT
Human intestinal organoids (HIOs) derived from pluripotent stem cells provide a valuable model for investigating human intestinal organogenesis and physiology, but they lack the immune components required to fully recapitulate the complexity of human intestinal biology and diseases. To address this issue and to begin to decipher human intestinal-immune crosstalk during development, we generated HIOs containing immune cells by transplanting HIOs under the kidney capsule of mice with a humanized immune system. We found that human immune cells temporally migrate to the mucosa and form cellular aggregates that resemble human intestinal lymphoid follicles. Moreover, after microbial exposure, epithelial microfold cells are increased in number, leading to immune cell activation determined by the secretion of IgA antibodies in the HIO lumen. This in vivo HIO system with human immune cells provides a framework for future studies on infection- or allergen-driven intestinal diseases.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplantes / Células-Tronco Pluripotentes Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplantes / Células-Tronco Pluripotentes Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article