Cutting Edge: TCR-β Selection Is Required at the CD4 + CD8 + Stage of Human T Cell Development

T cell development is predicated on the successful rearrangement of the TCR gene loci, which encode for Ag-specific receptors. Recombination-activating gene (RAG) 2 is required for TCR gene rearrangements, which occur during specific stages of T cell development. In this study, we differentiated hum...

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Veröffentlicht in:The Journal of immunology (1950) 2021-05, Vol.206 (10), p.2271-2276
Hauptverfasser: Chen, Edward L Y, Brauer, Patrick M, Martinez, Elisa C, Huang, Xiaotian, Yu, Ning, Anderson, Michele K, Li, Yang, Zúñiga-Pflücker, Juan Carlos
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Sprache:eng
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Zusammenfassung:T cell development is predicated on the successful rearrangement of the TCR gene loci, which encode for Ag-specific receptors. Recombination-activating gene (RAG) 2 is required for TCR gene rearrangements, which occur during specific stages of T cell development. In this study, we differentiated human pluripotent stem cells with a CRISPR/Cas9-directed deletion of the gene (RAG2-KO) to elucidate the requirement for the TCR β-chain in mediating β-selection during human T cell development. In stark contrast to mice, human RAG2-KO T lineage progenitors progressed to the CD4 CD8 double-positive (DP) stage in the absence of TCRβ rearrangements. Nonetheless, RAG2-KO DPs retrovirally transduced to express a rearranged TCR β-chain showed increased survival and proliferation as compared with control-transduced RAG2-KO DPs. Furthermore, transcriptomic analysis showed that TCRβ- and control-transduced RAG2-KO DPs differed in gene pathways related to survival and proliferation. Our results provide important insights as to the distinct requirement for the TCR β-chain during human T cell development.
ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.2100141