“9.61x6.69” b2815 Tissue Engineering and Nanotheranostics
Directed Differentiation of Human Pluripotent Stem Cells 95
able to generate VE-cadherin and PECAM-1 positive cells from both
hESCs and iPSCs and showed that these cells would form microcapil-
lary structures in hydrogels.^72
In 2014, Orlova et al. used a defined protocol to generate
endothelial cells from pluripotent stem cells.^73 They illustrated that by
culturing hPSCs with sequential additions of CHIR99021 and
Activin A followed by VEGF and SB431542, they were able to gener-
ate VE-cadherin positive endothelial progenitors which later expressed
CD34 and KDR.^73 Lian et al. published a simplified protocol using
only CHIR99021 in the initial differentiation step and a serum and
growth factor free media in later steps.74,75 This protocol produced
endothelial progenitors marked by CD34 and VE-cadherin expres-
sion within five days; however, interestingly the protocol was only
effective with male pluripotent stem cells.74,75 Future research is neces-
sary to optimize a differentiation technique that works for both male
and female cell lines with improved efficiency.
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