Fig. 4.
Fig. 4. CD4+ CD8+ human thymocytes are functional intermediates between CD3−CD4+ CD8− progenitors and CD4+ CD8β+ β-selected pre-T cells. (A) CD3− CD4+ CD8−thymocytes, isolated as described in Materials and Methods, were cultured in a hybrid hu/mo FTOC and analyzed after 4 and 11 days for the coexpression of CD4, CD8, and CD8β. (B) Intracytoplasmic TCRβ (TCRβic) expression (shaded areas) was analyzed by three-color flow cytometry in the cellular progeny recovered at day 4 of culture. By day 11, analysis was performed after electronic gating on the CD8+β− and the CD8+β+ progeny. Background fluorescence was determined with isotype-matched irrelevant MoAb. A representative experiment out of five is shown.

CD4+ CD8+ human thymocytes are functional intermediates between CD3CD4+ CD8 progenitors and CD4+ CD8β+ β-selected pre-T cells. (A) CD3 CD4+ CD8thymocytes, isolated as described in Materials and Methods, were cultured in a hybrid hu/mo FTOC and analyzed after 4 and 11 days for the coexpression of CD4, CD8, and CD8β. (B) Intracytoplasmic TCRβ (TCRβic) expression (shaded areas) was analyzed by three-color flow cytometry in the cellular progeny recovered at day 4 of culture. By day 11, analysis was performed after electronic gating on the CD8+β and the CD8+β+ progeny. Background fluorescence was determined with isotype-matched irrelevant MoAb. A representative experiment out of five is shown.

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