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dc.contributor.authorKashani, Elham
dc.contributor.authorFöhse, Lisa
dc.contributor.authorRaha, Solaiman
dc.contributor.authorSandrock, Inga
dc.contributor.authorOberdörfer, Linda
dc.contributor.authorKoenecke, Christian
dc.contributor.authorSuerbaum, Sebastian
dc.contributor.authorWeiss, Siegfried
dc.contributor.authorPrinz, Immo
dc.date.accessioned2016-06-03T10:28:26Zen
dc.date.available2016-06-03T10:28:26Zen
dc.date.issued2015en
dc.identifier.citationA clonotypic Vγ4Jγ1/Vδ5Dδ2Jδ1 innate γδ T-cell population restricted to the CCR6⁺CD27⁻ subset. 2015, 6:6477 Nat Communen
dc.identifier.issn2041-1723en
dc.identifier.pmid25765849en
dc.identifier.doi10.1038/ncomms7477en
dc.identifier.urihttp://hdl.handle.net/10033/611701en
dc.description.abstractHere 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.
dc.language.isoenen
dc.subject.meshAmino Acid Motifsen
dc.subject.meshAmino Acid Sequenceen
dc.subject.meshAnimalsen
dc.subject.meshAntigens, CD27en
dc.subject.meshCell Movementen
dc.subject.meshGerm-Line Mutationen
dc.subject.meshGreen Fluorescent Proteinsen
dc.subject.meshImmunity, Innateen
dc.subject.meshMiceen
dc.subject.meshMice, Inbred C57BLen
dc.subject.meshMice, Transgenicen
dc.subject.meshMolecular Sequence Dataen
dc.subject.meshPhenotypeen
dc.subject.meshPolymerase Chain Reactionen
dc.subject.meshReceptors, Antigen, T-Cell, gamma-deltaen
dc.subject.meshReceptors, CCR6en
dc.subject.meshSequence Analysis, DNAen
dc.subject.meshSingle-Cell Analysisen
dc.subject.meshT-Lymphocyte Subsetsen
dc.subject.meshThymus Glanden
dc.subject.meshTissue Distributionen
dc.titleA clonotypic Vγ4Jγ1/Vδ5Dδ2Jδ1 innate γδ T-cell population restricted to the CCR6⁺CD27⁻ subset.en
dc.typeArticleen
dc.contributor.departmentHelmholtz Centre for infection research, Inhoffenstr. 7, 38124 Braunschweig, Germany.en
dc.identifier.journalNature communicationsen
refterms.dateFOA2018-06-13T00:44:15Z
html.description.abstractHere 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.


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