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Fig. 1 | Stem Cell Research & Therapy

Fig. 1

From: Endothelial progenitor cells transplantation attenuated blood-brain barrier damage after ischemia in diabetic mice via HIF-1α

Fig. 1

EPC isolation and identification. A Morphology of EPCs from initial seeding to passage 4 in cell culture. The cells showed different morphology throughout the time course. a Round monocytes with dispersal distribution were observed soon after seeding. b Early EPCs formed colonies at 7 days after seeding. c Expended EPCs formed colonies 21 days after seeding. d Expended EPCs were nearly confluent on day 28. e Passage 3 and (f) passage 4, EPC presented cobblestone phenotype. Scale bar = 50 μm. B Flow cytometric analysis showed the percentage of cultured EPC cells (about 50 days) with surface markers KDR+/CD34+, KDR+/CD31+, KDR+/CD133+ and isotype control (from left to right). C Flow cytometric analysis showed the percentage of culture EPC cells (about 50 days) with surface markers CD45+, CD 29+ and CD90+. D Cell immunofluorescent staining showed KDR+/CD34+, CD31+/vWF+ cells (about 50 days). Scale bar = 50 μm

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