Cargando…
Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment
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 o...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106291/ https://www.ncbi.nlm.nih.gov/pubmed/35559672 http://dx.doi.org/10.1126/sciadv.abm9844 |
_version_ | 1784708249249906688 |
---|---|
author | Handel, Adam E. Cheuk, Stanley Dhalla, Fatima Maio, Stefano Hübscher, Tania Rota, Ioanna Deadman, Mary E. Ekwall, Olov Lütolf, Matthias Weinberg, Kenneth Holländer, Georg |
author_facet | Handel, Adam E. Cheuk, Stanley Dhalla, Fatima Maio, Stefano Hübscher, Tania Rota, Ioanna Deadman, Mary E. Ekwall, Olov Lütolf, Matthias Weinberg, Kenneth Holländer, Georg |
author_sort | Handel, Adam E. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9106291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91062912022-05-26 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 Sci Adv Biomedicine and Life Sciences 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. American Association for the Advancement of Science 2022-05-13 /pmc/articles/PMC9106291/ /pubmed/35559672 http://dx.doi.org/10.1126/sciadv.abm9844 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Handel, Adam E. Cheuk, Stanley Dhalla, Fatima Maio, Stefano Hübscher, Tania Rota, Ioanna Deadman, Mary E. Ekwall, Olov Lütolf, Matthias Weinberg, Kenneth Holländer, Georg Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment |
title | Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment |
title_full | Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment |
title_fullStr | Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment |
title_full_unstemmed | Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment |
title_short | Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment |
title_sort | developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9106291/ https://www.ncbi.nlm.nih.gov/pubmed/35559672 http://dx.doi.org/10.1126/sciadv.abm9844 |
work_keys_str_mv | AT handeladame developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT cheukstanley developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT dhallafatima developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT maiostefano developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT hubschertania developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT rotaioanna developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT deadmanmarye developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT ekwallolov developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT lutolfmatthias developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT weinbergkenneth developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment AT hollandergeorg developmentaldynamicsoftheneuralcrestmesenchymalaxisincreatingthethymicmicroenvironment |