| Literature DB >> 33941655 |
Edward L Y Chen1,2, Patrick M Brauer2, Elisa C Martinez2, Xiaotian Huang3, Ning Yu3, Michele K Anderson1,2, Yang Li4, Juan Carlos Zúñiga-Pflücker5,2.
Abstract
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 RAG2 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.Entities:
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Year: 2021 PMID: 33941655 PMCID: PMC8274368 DOI: 10.4049/jimmunol.2100141
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422