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   <subfield code="a">10.1007/s00251-006-0122-5</subfield>
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   <subfield code="a">Differential TCR gene usage between WC1 − and WC1 + ruminant γδ T cell subpopulations including those responding to bacterial antigen</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Seth Blumerman, Carolyn Herzig, Aric Rogers, Janice Telfer, Cynthia Baldwin]</subfield>
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   <subfield code="a">Ruminant γδ T cells are divided into subpopulations based on the presence or absence of WC1 co-receptors (scavenger-receptor-cysteine-rich family members uniquely expressed on γδ T cells). Evidence suggests WC1+ are inflammatory while WC1− are regulatory and that they also differ in their tissue distribution. Recently, this paradigm was refined further as cells that produce interferon-γ and proliferate to autologous antigens, leptospira antigens, or IL-12 were largely found within the WC1+ subpopulation that bears the WC1.1 antigenic epitope but not that bearing the WC1.2 epitope. Here, the T cell receptor gene expression by these different subpopulations (WC1−, WC1.1+, and WC1.2+) was compared using flow cytometrically-purified cells and reverse transcriptase-polymerase chain reaction (RT-PCR). The WC1− γδ T cells had transcripts for all 11 possible combinations of the TRG subgroup V and C genes while those in both WC1+ subpopulations were restricted to TRGV3-TRGC5 and TRGV7-TRGC5. In contrast, all three subpopulations expressed transcripts from all four known bovine TRDV genes. Further analysis of the WC1+ γδ T cells that proliferated in leptospira antigen-stimulated cultures indicated that they do not represent a unique subpopulation within the larger WC1+ population based on their TCR gene usage. Moreover, sequencing of 65 transcripts showed that their junctional regions were diverse as TRGJ5-1, TRGJ5-2, TRDJ1, and TRDJ3 were used, and CDR3s ranged from 9 to 24 amino acids. The restricted but shared γδ TCR gene usage for WC1.1 + , WC1.2+, and WC1+-antigen-responsive cells leaves open the possibility that the WC1 co-receptor is an important determining element in the activation process and subsequent response.</subfield>
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   <subfield code="a">Springer-Verlag, 2006</subfield>
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   <subfield code="a">γδ T cells</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">γδ T cell receptor</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">γδ T cell receptor genes</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">WC1</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Ruminant</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Blumerman</subfield>
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   <subfield code="u">Department of Veterinary and Animal Sciences, University of Massachusetts, 01003, Amherst, MA, USA</subfield>
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   <subfield code="a">Herzig</subfield>
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   <subfield code="u">Department of Veterinary and Animal Sciences, University of Massachusetts, 01003, Amherst, MA, USA</subfield>
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   <subfield code="a">Rogers</subfield>
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   <subfield code="u">Program in Molecular and Cellular Biology, University of Massachusetts, 01003, Amherst, MA, USA</subfield>
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   <subfield code="a">Telfer</subfield>
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   <subfield code="u">Department of Veterinary and Animal Sciences, University of Massachusetts, 01003, Amherst, MA, USA</subfield>
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   <subfield code="a">Baldwin</subfield>
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   <subfield code="u">Department of Veterinary and Animal Sciences, University of Massachusetts, 01003, Amherst, MA, USA</subfield>
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   <subfield code="t">Immunogenetics</subfield>
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   <subfield code="g">58/8(2006-08-01), 680-692</subfield>
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   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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