Fig. 3.
Fig. 3. Expansion of AGM- or FL-derived CD34+/c-Kit+ cells in the FL microenvironment. / CD34+/c-Kit+ cells were sorted from E11.5 AGM, E14.5 FL, or E18.5 FL and cultured in the E14.5 FL microenvironment. The number of GFP+ floating cells generated over the stromal layer was counted by FACS on day 10. Under these culture conditions, 40% to 80% of floating cells were GFP+. Results are shown as fold expansion relative to the number of input CD34+/c-Kit+ cells in each culture condition. (Lane a) Whole AGM cells from 3 embryos containing 1.8 × 104 CD34+/c-Kit+ cells were cultured in the microenvironment created by the AGM cells. (Lanes b-d) Whole AGM cells (1 × 105) containing 2 × 103 CD34+/c-Kit+ cells were cocultured in the FL microenvironment in the presence of various factors, as indicated. (Lanes e-m) CD34+/c-Kit+cells (2 × 103) from different sources were cultured in the FL microenvironment under various culture conditions. Data shown are the mean ± SD of at least triplicate experiments.

Expansion of AGM- or FL-derived CD34+/c-Kit+ cells in the FL microenvironment.

CD34+/c-Kit+ cells were sorted from E11.5 AGM, E14.5 FL, or E18.5 FL and cultured in the E14.5 FL microenvironment. The number of GFP+ floating cells generated over the stromal layer was counted by FACS on day 10. Under these culture conditions, 40% to 80% of floating cells were GFP+. Results are shown as fold expansion relative to the number of input CD34+/c-Kit+ cells in each culture condition. (Lane a) Whole AGM cells from 3 embryos containing 1.8 × 104 CD34+/c-Kit+ cells were cultured in the microenvironment created by the AGM cells. (Lanes b-d) Whole AGM cells (1 × 105) containing 2 × 103 CD34+/c-Kit+ cells were cocultured in the FL microenvironment in the presence of various factors, as indicated. (Lanes e-m) CD34+/c-Kit+cells (2 × 103) from different sources were cultured in the FL microenvironment under various culture conditions. Data shown are the mean ± SD of at least triplicate experiments.

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