Fig. 4.
Fig. 4. ES cell–derived megakaryocyte maturation. / Blast cell colony cells derived from mpl−/− flmpl, mpl−/− Δ3mpl, mpl−/− Δ34mpl ES cells were plated in serum-free liquid medium in the presence of PEG-rhuMGDF and were cultured for 5 days. (A) Megakaryocyte displaying proplatelets (arrows) (magnification × 200). (B) Ploidy analysis of megakaryocytes. After labeling with anti-CD41 antibody to identify megakaryocytes, cells were labeled with propidium iodide to evaluate DNA content. DNA content was scored on CD41+ cells. Images were made with Adobe Photoshop 5.0. (C) Flow cytometry quantification of platelets, defined as CD41+ elements with the same scatter properties as murine blood platelets (dot plot). SSC indicates side scatter; FSC, forward scatter.

ES cell–derived megakaryocyte maturation.

Blast cell colony cells derived from mpl−/− flmpl, mpl−/− Δ3mpl, mpl−/− Δ34mpl ES cells were plated in serum-free liquid medium in the presence of PEG-rhuMGDF and were cultured for 5 days. (A) Megakaryocyte displaying proplatelets (arrows) (magnification × 200). (B) Ploidy analysis of megakaryocytes. After labeling with anti-CD41 antibody to identify megakaryocytes, cells were labeled with propidium iodide to evaluate DNA content. DNA content was scored on CD41+ cells. Images were made with Adobe Photoshop 5.0. (C) Flow cytometry quantification of platelets, defined as CD41+ elements with the same scatter properties as murine blood platelets (dot plot). SSC indicates side scatter; FSC, forward scatter.

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