| Literature DB >> 33397934 |
Mohammad M Karimi1,2, Ya Guo1,3, Xiaokai Cui1, Husayn A Pallikonda1, Veronika Horková4, Yi-Fang Wang1, Sara Ruiz Gil5, Gustavo Rodriguez-Esteban5, Irene Robles-Rebollo1, Ludovica Bruno1, Radina Georgieva1, Bhavik Patel1, James Elliott1, Marian H Dore1, Danielle Dauphars6, Michael S Krangel6, Boris Lenhard1, Holger Heyn5, Amanda G Fisher1, Ondřej Štěpánek4, Matthias Merkenschlager7.
Abstract
CD4 and CD8 mark helper and cytotoxic T cell lineages, respectively, and serve as coreceptors for MHC-restricted TCR recognition. How coreceptor expression is matched with TCR specificity is central to understanding CD4/CD8 lineage choice, but visualising coreceptor gene activity in individual selection intermediates has been technically challenging. It therefore remains unclear whether the sequence of coreceptor gene expression in selection intermediates follows a stereotypic pattern, or is responsive to signaling. Here we use single cell RNA sequencing (scRNA-seq) to classify mouse thymocyte selection intermediates by coreceptor gene expression. In the unperturbed thymus, Cd4+Cd8a- selection intermediates appear before Cd4-Cd8a+ selection intermediates, but the timing of these subsets is flexible according to the strength of TCR signals. Our data show that selection intermediates discriminate MHC class prior to the loss of coreceptor expression and suggest a model where signal strength informs the timing of coreceptor gene activity and ultimately CD4/CD8 lineage choice.Entities:
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Year: 2021 PMID: 33397934 PMCID: PMC7782583 DOI: 10.1038/s41467-020-20306-w
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919