FIGURE SUMMARY
Title

Differentiation of Human Pluripotent Stem Cells into Functional Endothelial Cells in Scalable Suspension Culture

Authors
Olmer, R., Engels, L., Usman, A., Menke, S., Malik, M.N.H., Pessler, F., Göhring, G., Bornhorst, D., Bolten, S., Abdelilah-Seyfried, S., Scheper, T., Kempf, H., Zweigerdt, R., Martin, U.
Source
Full text @ Stem Cell Reports

Vascular Competence of Early and Late hiPSC-Derived EC Passages in a Zebrafish Xenograft Model

Early (P1) passage hiPSC-ECs (green, hCBiPSCAGeGFP) within the embryonic zebrafish vasculature [marked by Tg(fli1a:mCherry-NLS)ubs10, red)] 1 day after transplantation (A). Scale bar, 300 μm. Details of vessels with P1 hiPSC-EC (green) integration into the Tg(fli1a:mCherry-NLS)ubs10 transgenic embryonic zebrafish vasculature (red) (B–D). Scale bar, 50 μm. Late (P11) passage hiPSC-ECs (green) within the Tg(fli1a:mCherry-NLS)ubs10 transgenic embryonic zebrafish vasculature (red) 1 day after transplantation (E). Scale bar, 300 μm. Details of vessel with P11 hiPSC-EC (green) integration into the Tg(fli1a:mCherry-NLS)ubs10 transgenic embryonic zebrafish vasculature (red) (F–H). Scale bar, 50 μm. Quantification of integration rates of early and late hiPSC-ECs compared with early (P1, P4, and P5) and late (P14) hUVECs into the zebrafish embryonic vasculature 1 day after transplantation. Integration rates into the zebrafish vasculature were 61.9% (n = 83/134 embryos) for early hiPSC-ECs and 78.3% (n = 112/143 embryos) for late hiPSC-ECs. ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001 (I).

Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Stem Cell Reports