作者
Jong-Eun Park,Rachel A. Botting,Cecilia Domínguez Conde,Dorin-Mirel Popescu,Marieke Lavaert,Daniel J. Kunz,Emily Stephenson,Roberta Ragazzini,Elizabeth Tuck,Anna Wilbrey-Clark,John R. Ferdinand,Simone Webb,Daniel Maunder,Niels Vandamme,Krishnaa T. Mahbubani,Krzysztof Polański,Lira Mamanova,Andrew Fuller,Andrew Filby,Gary Reynolds,David Dixon,Kourosh Saeb‐Parsy,Steven Lisgo,Deborah J. Henderson,Roser Vento‐Tormo,Kerstin B. Meyer,Yvan Saeys,Paola Bonfanti,Sam Behjati,Menna R. Clatworthy,Tom Taghon,Muzlifah Haniffa,Sarah A. Teichmann
摘要
Abstract The thymus provides a nurturing environment for the differentiation and selection of T cells, a process orchestrated by their interaction with multiple thymic cell types. We utilised single-cell RNA-sequencing (scRNA-seq) to create a cell census of the human thymus and to reconstruct T-cell differentiation trajectories and T-cell receptor (TCR) recombination kinetics. Using this approach, we identified and located in situ novel CD8αα + T-cell populations, thymic fibroblast subtypes and activated dendritic cell (aDC) states. In addition, we reveal a bias in TCR recombination and selection, which is attributed to genomic position and suggests later commitment of the CD8 + T-cell lineage. Taken together, our data provide a comprehensive atlas of the human thymus across the lifespan with new insights into human T-cell development.