Figure 8
Figure 8. Analysis of ex vivo platelet release by Mks differentiated from adult human peripheral blood hematopoietic progenitors. (A) Confocal microscopy imaging of Mks from 1 healthy control and 2 patients within the silk-based bone marrow system. (Ai-Aiii) Imaging of mature Mks immediately after seeding into the silk sponge (green = CD61; blue = nuclei; scale bar = 50 μm). (Aiv-Avi) Mks forming proplatelet through the silk microtube wall (green = CD61; blue = nuclei; scale bar = 50 μm). Arrows indicate proplatelet branching and elongation. Silk fibroin 3D scaffolds were stained with Hoechst 33258 and visualized in blue. (B) Flow cytometry analysis of ex vivo-produced platelets. Samples were mixed with counting beads to quantify the number of CD61+CD42b+ platelets. (C) Comparison of platelet count between in vivo and ex vivo quantified numbers.

Analysis of ex vivo platelet release by Mks differentiated from adult human peripheral blood hematopoietic progenitors. (A) Confocal microscopy imaging of Mks from 1 healthy control and 2 patients within the silk-based bone marrow system. (Ai-Aiii) Imaging of mature Mks immediately after seeding into the silk sponge (green = CD61; blue = nuclei; scale bar = 50 μm). (Aiv-Avi) Mks forming proplatelet through the silk microtube wall (green = CD61; blue = nuclei; scale bar = 50 μm). Arrows indicate proplatelet branching and elongation. Silk fibroin 3D scaffolds were stained with Hoechst 33258 and visualized in blue. (B) Flow cytometry analysis of ex vivo-produced platelets. Samples were mixed with counting beads to quantify the number of CD61+CD42b+ platelets. (C) Comparison of platelet count between in vivo and ex vivo quantified numbers.

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