Derivation of endothelial cells from hESCs
Reference . | ES source . | EC derivation . |
---|---|---|
Kaufman24 | hES cells (H1, H1.1, and H9.2) | Undifferentiated hESCs were grown on mouse bone marrow cells (S17) or mouse yolk sac endothelial cells (c166) for 17 days. |
Wang33 | Human EBs (H9, H1) days 9-10 | EBs were sorted by FACS for VE-cadherin/PECAM1+ cells and then the sorted cells were grown for 7 days in endothelial-supporting media containing pituitary extracts and VEGF. |
Levenberg et al29 | Human EBs (H9) day 13 | FACS sorting for PECAM1+ cells. |
Gerecht-Nir et al36 | hES cells (H9, H13, I9) | Undifferentiated hESCs were grown on IV collagen–coated dishes, filtered (40 μm mesh), and then recultured on IV collagen–coated dishes supplanted with VEGF. |
Vodyanik41 | Undifferentiated hES cells (H1, H9) | Undifferentiated hES cells were grown on mouse bone marrow stromal cells (OP9, S17, and MS-5) for 10 days. |
Zambidis34 | Human EBs (H1) days 7-9 | EBs were grown on methylcellulose and supplemented with 50 μg/mL ascorbic acid, 0.5% insulin/transferring/selenium. |
Reference . | ES source . | EC derivation . |
---|---|---|
Kaufman24 | hES cells (H1, H1.1, and H9.2) | Undifferentiated hESCs were grown on mouse bone marrow cells (S17) or mouse yolk sac endothelial cells (c166) for 17 days. |
Wang33 | Human EBs (H9, H1) days 9-10 | EBs were sorted by FACS for VE-cadherin/PECAM1+ cells and then the sorted cells were grown for 7 days in endothelial-supporting media containing pituitary extracts and VEGF. |
Levenberg et al29 | Human EBs (H9) day 13 | FACS sorting for PECAM1+ cells. |
Gerecht-Nir et al36 | hES cells (H9, H13, I9) | Undifferentiated hESCs were grown on IV collagen–coated dishes, filtered (40 μm mesh), and then recultured on IV collagen–coated dishes supplanted with VEGF. |
Vodyanik41 | Undifferentiated hES cells (H1, H9) | Undifferentiated hES cells were grown on mouse bone marrow stromal cells (OP9, S17, and MS-5) for 10 days. |
Zambidis34 | Human EBs (H1) days 7-9 | EBs were grown on methylcellulose and supplemented with 50 μg/mL ascorbic acid, 0.5% insulin/transferring/selenium. |
Summary of experiments in which hESCs were used to derive endothelial potential, indicating the source of the hESCs and the derivation procedure.