Fig. 2.
Fig. 2. Development and peripheral maintenance of CD8+ T lymphocytes in K14-β2m mice. / (A) Thymocytes from K14-β2m mice and β2m+/° littermates were triply stained with anti-CD4, anti-CD8, and anti-TCRβ antibodies. Percentages (mean ± SD, n = 6) of CD4−CD8−, CD4+CD8+, CD4+CD8−TCRhigh and CD4−CD8+TCRhigh cells are indicated. Thymi from K14-β2m mice and β2m+/° littermates contained 127 ± 45 × 106 and 116 ± 25 × 106 cells, respectively. Spleen and lymph node cell suspensions were stained with anti-CD8 and anti-TCRβ antibodies (n = 3). K14-β2m mice and β2m+/° littermates had 98 ± 26 × 106 and 107 ± 25 × 106 splenocytes and 20 ± 6 × 106 and 28 ± 2 × 106 lymph node cells, respectively. (B) Expression of memory/activation markers by CD8+ splenocytes from K14-β2m mice and β2m+/° littermates. Cells were stained with anti-TCRβ, anti-CD8, and anti-CD44, anti-CD62L or anti-CD69 antibodies. Representative histograms of electronically gated TCRβ+CD8+ cells are shown.

Development and peripheral maintenance of CD8+ T lymphocytes in K14-β2m mice.

(A) Thymocytes from K14-β2m mice and β2m+/° littermates were triply stained with anti-CD4, anti-CD8, and anti-TCRβ antibodies. Percentages (mean ± SD, n = 6) of CD4CD8, CD4+CD8+, CD4+CD8TCRhigh and CD4CD8+TCRhigh cells are indicated. Thymi from K14-β2m mice and β2m+/° littermates contained 127 ± 45 × 106 and 116 ± 25 × 106 cells, respectively. Spleen and lymph node cell suspensions were stained with anti-CD8 and anti-TCRβ antibodies (n = 3). K14-β2m mice and β2m+/° littermates had 98 ± 26 × 106 and 107 ± 25 × 106 splenocytes and 20 ± 6 × 106 and 28 ± 2 × 106 lymph node cells, respectively. (B) Expression of memory/activation markers by CD8+ splenocytes from K14-β2m mice and β2m+/° littermates. Cells were stained with anti-TCRβ, anti-CD8, and anti-CD44, anti-CD62L or anti-CD69 antibodies. Representative histograms of electronically gated TCRβ+CD8+ cells are shown.

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