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Developmental dynamics of the neural crest-mesenchymal axis in creating the thymic microenvironment.
Handel, Adam E; Cheuk, Stanley; Dhalla, Fatima; Maio, Stefano; Hübscher, Tania; Rota, Ioanna; Deadman, Mary E; Ekwall, Olov; Lütolf, Matthias; Weinberg, Kenneth; Holländer, Georg.
Afiliação
  • Handel AE; Department of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Cheuk S; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
  • Dhalla F; Department of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Maio S; Department of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden.
  • Hübscher T; Department of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Rota I; Department of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Deadman ME; Laboratory of Stem Cell Bioengineering, Swiss Federal Institute of Technology in Lausanne, Lausanne, Switzerland.
  • Ekwall O; Department of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Lütolf M; Department of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Weinberg K; Department of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden.
  • Holländer G; Department of Pediatrics, University of Gothenburg, Gothenburg, Sweden.
Sci Adv ; 8(19): eabm9844, 2022 May 13.
Article em En | MEDLINE | ID: mdl-35559672
ABSTRACT
The thymic stroma is composed of epithelial and nonepithelial cells providing separate microenvironments controlling homing, differentiation, and selection of hematopoietic precursor cells to functional T cells. Here, we explore at single-cell resolution the complex composition and dynamic changes of the nonepithelial stromal compartment across different developmental stages in the human and mouse thymus, and in an experimental model of the DiGeorge syndrome, the most common form of human thymic hypoplasia. The detected gene expression signatures identify previously unknown stromal subtypes and relate their individual molecular profiles to separate differentiation trajectories and functions, revealing an unprecedented heterogeneity of different cell types that emerge at discrete developmental stages and vary in their expression of key regulatory signaling circuits and extracellular matrix components. Together, these findings highlight the dynamic complexity of the nonepithelial thymus stroma and link this to separate instructive roles essential for normal thymus organogenesis and tissue maintenance.

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Sci Adv Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Sci Adv Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido