Figure 4
Figure 4. Lack of permanent TCRγ silencing in innate T cells. (A) Expression of TCRVγ4 mRNA normalized to β-actin in the indicated subpopulations, measured by real time RT-PCR in arbitrary units relative to mature thymocytes (AU). N indicates naive splenocytes TCRγδ−TCRβ+CD44−CD62L+; M, memory splenocytes TCRγδ−TCRβ+CD44+CD62L+; A, activated splenocytes TCRγδ−TCRβ+CD44+CD62L−; T, mature thymocytes TCRγδ−TCRβhi; and NKT, thymic NKT TCRγδ−TCRβloNK1.1+. (B-C) Analysis of MACS enriched, CD1dtet+ iNKT cells from the thymus of TCRδ−/− and CD1d−/−TCRδ−/− (B) and the sorted CD1dtet+ T-cell subsets from TCRδ−/− mice. (C) Numbers in dot plots show percentages. (D) Expression of TCRVγ4 mRNA normalized to cell number in the indicated subpopulations sorted from TCRδ−/− and CD1d−/−TCRδ−/− mice measured by real-time RT-PCR (see “Two-stage RT-PCR”) in arbitrary units relative to DN thymocytes (AU).

Lack of permanent TCRγ silencing in innate T cells. (A) Expression of TCRVγ4 mRNA normalized to β-actin in the indicated subpopulations, measured by real time RT-PCR in arbitrary units relative to mature thymocytes (AU). N indicates naive splenocytes TCRγδTCRβ+CD44CD62L+; M, memory splenocytes TCRγδTCRβ+CD44+CD62L+; A, activated splenocytes TCRγδTCRβ+CD44+CD62L; T, mature thymocytes TCRγδTCRβhi; and NKT, thymic NKT TCRγδTCRβloNK1.1+. (B-C) Analysis of MACS enriched, CD1dtet+ iNKT cells from the thymus of TCRδ−/− and CD1d−/−TCRδ−/− (B) and the sorted CD1dtet+ T-cell subsets from TCRδ−/− mice. (C) Numbers in dot plots show percentages. (D) Expression of TCRVγ4 mRNA normalized to cell number in the indicated subpopulations sorted from TCRδ−/− and CD1d−/−TCRδ−/− mice measured by real-time RT-PCR (see “Two-stage RT-PCR”) in arbitrary units relative to DN thymocytes (AU).

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