Fig. 4.
Fig. 4. Analysis of Ik7-infected CD34+ cells. / (A) Representative flow cytometric analysis of CD34+ cells cultured for a total of 4 days and having been infected with virus for 2 days (pre-sort). Reanalysis of CD34+EGFP− and EGFP+ cells from these cultures (CD34+ E− and CD34+E+), which are being used to assay DC hematopoiesis. (B) RT-PCR analysis of Ikaros mRNA in the sorted CD34+ cell populations showing the presence of the multiple endogenous Ikaros isoforms Ik1 (888 bp), Ik2/3 (630 bp), Ik4 (500 bp), and the 467 bp-specific product corresponding to Ik7. (C) Detection of DC activity by MLR. Stimulator cells were obtained after Ik7 infection and culture in FKGm17 of CD34+ EGFP+ cells (closed squares) or CD34+ EGFP− cells (open diamonds) and the response of purified T cells was measured as CPM after3H-thymidine incorporation.

Analysis of Ik7-infected CD34+ cells.

(A) Representative flow cytometric analysis of CD34+ cells cultured for a total of 4 days and having been infected with virus for 2 days (pre-sort). Reanalysis of CD34+EGFP and EGFP+ cells from these cultures (CD34+ E and CD34+E+), which are being used to assay DC hematopoiesis. (B) RT-PCR analysis of Ikaros mRNA in the sorted CD34+ cell populations showing the presence of the multiple endogenous Ikaros isoforms Ik1 (888 bp), Ik2/3 (630 bp), Ik4 (500 bp), and the 467 bp-specific product corresponding to Ik7. (C) Detection of DC activity by MLR. Stimulator cells were obtained after Ik7 infection and culture in FKGm17 of CD34+ EGFP+ cells (closed squares) or CD34+ EGFP cells (open diamonds) and the response of purified T cells was measured as CPM after3H-thymidine incorporation.

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