Your browser doesn't support javascript.
loading
Cells of the human intestinal tract mapped across space and time.
Elmentaite, Rasa; Kumasaka, Natsuhiko; Roberts, Kenny; Fleming, Aaron; Dann, Emma; King, Hamish W; Kleshchevnikov, Vitalii; Dabrowska, Monika; Pritchard, Sophie; Bolt, Liam; Vieira, Sara F; Mamanova, Lira; Huang, Ni; Perrone, Francesca; Goh Kai'En, Issac; Lisgo, Steven N; Katan, Matilda; Leonard, Steven; Oliver, Thomas R W; Hook, C Elizabeth; Nayak, Komal; Campos, Lia S; Domínguez Conde, Cecilia; Stephenson, Emily; Engelbert, Justin; Botting, Rachel A; Polanski, Krzysztof; van Dongen, Stijn; Patel, Minal; Morgan, Michael D; Marioni, John C; Bayraktar, Omer Ali; Meyer, Kerstin B; He, Xiaoling; Barker, Roger A; Uhlig, Holm H; Mahbubani, Krishnaa T; Saeb-Parsy, Kourosh; Zilbauer, Matthias; Clatworthy, Menna R; Haniffa, Muzlifah; James, Kylie R; Teichmann, Sarah A.
Afiliação
  • Elmentaite R; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Kumasaka N; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Roberts K; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Fleming A; Molecular Immunity Unit, Department of Medicine, University of Cambridge, MRC Laboratory of Molecular Biology, Cambridge, UK.
  • Dann E; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • King HW; Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London, UK.
  • Kleshchevnikov V; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Dabrowska M; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Pritchard S; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Bolt L; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Vieira SF; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Mamanova L; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Huang N; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Perrone F; Department of Paediatrics, University of Cambridge, Cambridge, UK.
  • Goh Kai'En I; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Lisgo SN; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Katan M; Structural and Molecular Biology, Division of Biosciences, University College London, London, UK.
  • Leonard S; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Oliver TRW; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Hook CE; Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Nayak K; Department of Histopathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Campos LS; Department of Paediatrics, University of Cambridge, Cambridge, UK.
  • Domínguez Conde C; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Stephenson E; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Engelbert J; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Botting RA; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Polanski K; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • van Dongen S; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Patel M; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Morgan MD; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Marioni JC; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Cambridge, UK.
  • Bayraktar OA; Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
  • Meyer KB; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • He X; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Cambridge, UK.
  • Barker RA; Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
  • Uhlig HH; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Mahbubani KT; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Saeb-Parsy K; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences and Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
  • Zilbauer M; John van Geest Centre for Brain Repair, Department of Clinical Neurosciences and Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
  • Clatworthy MR; Translational Gastroenterology Unit, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • Haniffa M; Department of Paediatrics, University of Oxford, Oxford, UK.
  • James KR; NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Teichmann SA; Department of Surgery, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Cambridge, UK.
Nature ; 597(7875): 250-255, 2021 09.
Article em En | MEDLINE | ID: mdl-34497389
ABSTRACT
The cellular landscape of the human intestinal tract is dynamic throughout life, developing in utero and changing in response to functional requirements and environmental exposures. Here, to comprehensively map cell lineages, we use single-cell RNA sequencing and antigen receptor analysis of almost half a million cells from up to 5 anatomical regions in the developing and up to 11 distinct anatomical regions in the healthy paediatric and adult human gut. This reveals the existence of transcriptionally distinct BEST4 epithelial cells throughout the human intestinal tract. Furthermore, we implicate IgG sensing as a function of intestinal tuft cells. We describe neural cell populations in the developing enteric nervous system, and predict cell-type-specific expression of genes associated with Hirschsprung's disease. Finally, using a systems approach, we identify key cell players that drive the formation of secondary lymphoid tissue in early human development. We show that these programs are adopted in inflammatory bowel disease to recruit and retain immune cells at the site of inflammation. This catalogue of intestinal cells will provide new insights into cellular programs in development, homeostasis and disease.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Envelhecimento / Saúde / Sistema Nervoso Entérico / Feto / Intestinos / Linfonodos Tipo de estudo: Prognostic_studies Limite: Adult / Animals / Child / Female / Humans Idioma: En Revista: Nature Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Envelhecimento / Saúde / Sistema Nervoso Entérico / Feto / Intestinos / Linfonodos Tipo de estudo: Prognostic_studies Limite: Adult / Animals / Child / Female / Humans Idioma: En Revista: Nature Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido
...