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A spatial human thymus cell atlas mapped to a continuous tissue axis.
Yayon, Nadav; Kedlian, Veronika R; Boehme, Lena; Suo, Chenqu; Wachter, Brianna; Beuschel, Rebecca T; Amsalem, Oren; Polanski, Krzysztof; Koplev, Simon; Tuck, Elizabeth; Dann, Emma; Van Hulle, Jolien; Perera, Shani; Putteman, Tom; Predeus, Alexander V; Dabrowska, Monika; Richardson, Laura; Tudor, Catherine; Kreins, Alexandra Y; Engelbert, Justin; Stephenson, Emily; Kleshchevnikov, Vitalii; De Rita, Fabrizio; Crossland, David; Bosticardo, Marita; Pala, Francesca; Prigmore, Elena; Chipampe, Nana-Jane; Prete, Martin; Fei, Lijiang; To, Ken; Barker, Roger A; He, Xiaoling; Van Nieuwerburgh, Filip; Bayraktar, Omer; Patel, Minal; Davies, Graham E; Haniffa, Muzlifah A; Uhlmann, Virginie; Notarangelo, Luigi D; Germain, Ronald N; Radtke, Andrea J; Marioni, John C; Taghon, Tom; Teichmann, Sarah A.
Afiliação
  • Yayon N; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Kedlian VR; European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, United Kingdom.
  • Boehme L; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Suo C; Ghent University, Department of Diagnostic Sciences, Ghent, Belgium.
  • Wachter B; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Beuschel RT; National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.
  • Amsalem O; National Institute of Allergy and Infectious Diseases, NIH, Lymphocyte Biology Section and Center for Advanced Tissue Imaging, Bethesda, MD, United States.
  • Polanski K; Beth Israel Deaconess Medical Center, Harvard Medical School, Division of Endocrinology, Diabetes and Metabolism, Boston, MA, United States.
  • Koplev S; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Tuck E; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Dann E; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Van Hulle J; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Perera S; Ghent University, Department of Diagnostic Sciences, Ghent, Belgium.
  • Putteman T; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Predeus AV; Ghent University, Department of Diagnostic Sciences, Ghent, Belgium.
  • Dabrowska M; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Richardson L; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Tudor C; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Kreins AY; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Engelbert J; Great Ormond Street Hospital for Children NHS Foundation Trust, Department of Immunology and Gene Therapy, London, United Kingdom.
  • Stephenson E; UCL Great Ormond Street Institute of Child Health, Infection, Immunity and Inflammation Research & Teaching Department, London, United Kingdom.
  • Kleshchevnikov V; Newcastle University, Biosciences Institute, Faculty of Medical Sciences, Newcastle upon Tyne, United Kingdom.
  • De Rita F; Newcastle University, Biosciences Institute, Faculty of Medical Sciences, Newcastle upon Tyne, United Kingdom.
  • Crossland D; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Bosticardo M; Freeman Hospital, Department of Adult Congenital Heart Disease and Paediatric Cardiology/Cardiothoracic Surgery, Newcastle upon Tyne, United Kingdom.
  • Pala F; Freeman Hospital, Department of Adult Congenital Heart Disease and Paediatric Cardiology/Cardiothoracic Surgery, Newcastle upon Tyne, United Kingdom.
  • Prigmore E; National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.
  • Chipampe NJ; National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.
  • Prete M; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Fei L; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • To K; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Barker RA; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • He X; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Van Nieuwerburgh F; University of Cambridge, John van Geest Centre for Brain Repair, Department of Clinical Neurosciences and Wellcome-MRC Cambridge Stem Cell Institute, Cambridge, United Kingdom.
  • Bayraktar O; University of Cambridge, John van Geest Centre for Brain Repair, Department of Clinical Neurosciences and Wellcome-MRC Cambridge Stem Cell Institute, Cambridge, United Kingdom.
  • Patel M; Ghent University, Laboratory of Pharmaceutical Biotechnology, Ghent, Belgium.
  • Davies GE; Cancer Research Institute Ghent (CRIG), Ghent, Belgium.
  • Haniffa MA; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Uhlmann V; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Notarangelo LD; Great Ormond Street Hospital for Children NHS Foundation Trust, Department of Immunology and Gene Therapy, London, United Kingdom.
  • Germain RN; UCL Great Ormond Street Institute of Child Health, Infection, Immunity and Inflammation Research & Teaching Department, London, United Kingdom.
  • Radtke AJ; Wellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
  • Marioni JC; Newcastle University, Biosciences Institute, Faculty of Medical Sciences, Newcastle upon Tyne, United Kingdom.
  • Taghon T; European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, United Kingdom.
  • Teichmann SA; National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.
bioRxiv ; 2023 Oct 27.
Article em En | MEDLINE | ID: mdl-37986877
T cells develop from circulating precursors, which enter the thymus and migrate throughout specialised sub-compartments to support maturation and selection. This process starts already in early fetal development and is highly active until the involution of the thymus in adolescence. To map the micro-anatomical underpinnings of this process in pre- vs. post-natal states, we undertook a spatially resolved analysis and established a new quantitative morphological framework for the thymus, the Cortico-Medullary Axis. Using this axis in conjunction with the curation of a multimodal single-cell, spatial transcriptomics and high-resolution multiplex imaging atlas, we show that canonical thymocyte trajectories and thymic epithelial cells are highly organised and fully established by post-conception week 12, pinpoint TEC progenitor states, find that TEC subsets and peripheral tissue genes are associated with Hassall's Corpuscles and uncover divergence in the pace and drivers of medullary entry between CD4 vs. CD8 T cell lineages. These findings are complemented with a holistic toolkit for spatial analysis and annotation, providing a basis for a detailed understanding of T lymphocyte development.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido