A spatial human thymus cell atlas mapped to a continuous tissue axis.
Nadav YayonVeronika R KedlianLena BoehmeChenqu SuoBrianna WachterRebecca T BeuschelOren AmsalemKrzysztof PolańskiSimon KoplevElizabeth TuckEmma DannJolien Van HulleShani PereraTom PuttemanAlexander V PredeusMonika DabrowskaLaura RichardsonCatherine TudorAlexandra Y KreinsJustin EngelbertEmily StephensonVitalii KleshchevnikovFabrizio De RitaDavid CrosslandMarita BosticardoFrancesca PalaElena PrigmoreNana-Jane ChipampeMartin PreteLijiang FeiKendrick ToRoger A BarkerXiaoling HeFilip Van NieuwerburghOmer BayraktarMinal PatelGraham E DaviesMuzlifah A HaniffaVirginie UhlmannLuigi Daniele NotarangeloRonald N GermainAndrea J RadtkeJohn C MarioniTom TaghonSarah A TeichmannPublished in: bioRxiv : the preprint server for biology (2023)
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.