| Literature DB >> 25765849 |
Elham Kashani1, Lisa Föhse1, Solaiman Raha1, Inga Sandrock1, Linda Oberdörfer1, Christian Koenecke2, Sebastian Suerbaum3, Siegfried Weiss4, Immo Prinz1.
Abstract
Here we investigate the TCR repertoire of mouse Vγ4(+) γδ T cells in correlation with their developmental origin and homeostasis. By deep sequencing we identify a high frequency of straight Vδ5Dδ2Jδ1 germline rearrangements without P- and N-nucleotides within the otherwise highly diverse Trd repertoire of Vγ4(+) cells. This sequence is infrequent in CCR6(-)CD27(+) cells, but abundant among CCR6(+)CD27(-) γδ T cells. Using an inducible Rag1 knock-in mouse model, we show that γδ T cells generated in the adult thymus rarely contain this germline-rearranged Vδ5Dδ2Jδ1 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 Vγ4(+)Vδ5(+) cells. In conclusion, this study identifies an innate subset of fetal thymus-derived γδ T cells with an invariant Vγ4(+)Vδ5(+) TCR that is restricted to the CCR6(+)CD27(-) subset of γδ T cells.Entities:
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Year: 2015 PMID: 25765849 DOI: 10.1038/ncomms7477
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919