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. 1999 Jun 22;96(13):7451–7455. doi: 10.1073/pnas.96.13.7451

Table 1.

γδ-IEL isolated from various mouse strains

Mice n γδ-IEL per mouse, × 106 Subset of γδ-IEL, %
Thy-1+ Vγ1+ Vγ4+ Vγ7+ Vδ4+
wt 8 3.05 ± 0.68 27.5 ± 10.9 34.7 ± 5.7 10.3 ± 4.1 52.8 ± 11.8 14.0 ± 3.6
β−/− 9 4.24 ± 1.06 23.1 ± 1.6 55.3 ± 4.5 8.2 ± 1.4 38.9 ± 7.0 11.3 ± 1.4
α−/− 8 4.90 ± 1.91 43.4 ± 12.0 45.5 ± 13.6 9.1 ± 7.6 43.5 ± 11.3 21.9 ± 5.8

IEL isolated from wt, β−/− and α−/− mice were incubated first with anti-Thy-1.2 mAb (biotinylated) and then with streptavidin–phycoerythrin and anti-TCR-γδ mAb (FITC-conjugated). These IEL were also incubated first with anti-Vγ1, anti-Vγ4, anti-Vγ7, or anti-Vδ4 mAb. After washing, the IEL were incubated with biotinylated goat anti-hamster IgG and subsequently counterstained with streptavidin-phycoerythrin and anti-TCR-γδ mAb (FITC-conjugated). The proportion of Thy-1+ cells in α−/− γδ-IEL was significantly higher than those in wt (P < 0.05) and β−/− (P < 0.01) γδ-IEL. The proportion of Vδ4+ cells in α−/− γδ-IEL was significantly higher than those in wt (P < 0.01) and β−/− (P < 0.01) γδ-IEL.