期刊
NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms7477
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资金
- Deutsche Forschungsgemeinschaft [DFG-PR727/4-1, DFG-PR727/5-1, DFG SFB 900/B8, DFG SFB 900/Z1]
Here we investigate the TCR repertoire of mouse V gamma 4(+) gamma delta T cells in correlation with their developmental origin and homeostasis. By deep sequencing we identify a high frequency of straight V delta 5D delta 2J delta 1 germline rearrangements without P- and N-nucleotides within the otherwise highly diverse Trd repertoire of V gamma 4(+) cells. This sequence is infrequent in CCR6(-)CD27(+) cells, but abundant among CCR6(+)CD27(-) gamma delta T cells. Using an inducible Rag1 knock-in mouse model, we show that gamma delta T cells generated in the adult thymus rarely contain this germline-rearranged V delta 5D delta 2J delta 1 sequence, confirming its fetal origin. Single-cell analysis and deep sequencing of the Trg locus reveal a dominant CDR3 junctional motif that completes the TCR repertoire of invariant V gamma 4(+)V delta 5(+) cells. In conclusion, this study identifies an innate subset of fetal thymus-derived gamma delta T cells with an invariant V gamma 4(+)V delta 5(+) TCR that is restricted to the CCR6(+)CD27(-) subset of gamma delta T cells.
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