A spatial human thymus cell atlas mapped to a continuous tissue axis
Author:
Yayon NadavORCID, Kedlian Veronika R.ORCID, Boehme LenaORCID, Suo ChenquORCID, Wachter BriannaORCID, Beuschel Rebecca T.ORCID, Amsalem OrenORCID, Polanski KrzysztofORCID, Koplev SimonORCID, Tuck Elizabeth, Dann EmmaORCID, Van Hulle JolienORCID, Perera ShaniORCID, Putteman TomORCID, Predeus Alexander V.ORCID, Dabrowska Monika, Richardson Laura, Tudor CatherineORCID, Kreins Alexandra Y.ORCID, Engelbert Justin, Stephenson EmilyORCID, Kleshchevnikov VitaliiORCID, De Rita Fabrizio, Crossland David, Bosticardo MaritaORCID, Pala Francesca, Prigmore Elena, Chipampe Nana-Jane, Prete MartinORCID, Fei Lijiang, To KenORCID, Barker Roger A., He Xiaoling, Van Nieuwerburgh FilipORCID, Bayraktar Omer, Patel Minal, Davies Graham E., Haniffa Muzlifah A.ORCID, Uhlmann VirginieORCID, Notarangelo Luigi D.ORCID, Germain Ronald N., Radtke Andrea J.ORCID, Marioni John C.ORCID, Taghon TomORCID, Teichmann Sarah A.ORCID
Abstract
AbstractT 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.
Publisher
Cold Spring Harbor Laboratory
Cited by
5 articles.
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