Figure 1.
Figure 1. Survival of CD4+ T cells in a lymphopenic environment does not depend on interactions with MHC class II molecules. CFSE-labeled lymph node CD4+ T cells (5 × 106) from normal C57BL6 mice were injected intravenously into CD3ϵ-/-mice and CD3ϵ-/-MHC IIΔ/Δ mice. At various times after transfer, lymph nodes and spleen were recovered and pooled, and single-cell suspensions were prepared. (A) CFSE fluorescence histograms of CD4+ TCRhicells are shown as a function of time after transfer. Histograms on the right are gated on CFSE+ CD4+ TCRhicells. (B) Absolute numbers of total, CFSE+, and CFSE- CD4+ TCRhicells are shown as a function of time after transfer. Data represent mean ± SD. (C) CD4, TCR, and CD44 fluorescence histograms of CFSE+ and CFSE- CD4+ T cells recovered 28 days after transfer are shown in comparison with CD4, TCR, and CD44 fluorescence histograms of control CD4+ T cells from normal C57BL/6 mice.

Survival of CD4+T cells in a lymphopenic environment does not depend on interactions with MHC class II molecules. CFSE-labeled lymph node CD4+ T cells (5 × 106) from normal C57BL6 mice were injected intravenously into CD3ϵ-/-mice and CD3ϵ-/-MHC IIΔ/Δ mice. At various times after transfer, lymph nodes and spleen were recovered and pooled, and single-cell suspensions were prepared. (A) CFSE fluorescence histograms of CD4+ TCRhicells are shown as a function of time after transfer. Histograms on the right are gated on CFSE+ CD4+ TCRhicells. (B) Absolute numbers of total, CFSE+, and CFSE- CD4+ TCRhicells are shown as a function of time after transfer. Data represent mean ± SD. (C) CD4, TCR, and CD44 fluorescence histograms of CFSE+ and CFSE- CD4+ T cells recovered 28 days after transfer are shown in comparison with CD4, TCR, and CD44 fluorescence histograms of control CD4+ T cells from normal C57BL/6 mice.

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