Table 2.
Subsets of EPC and EC from viable PBMC isolated from human blood (n=8) (Mean ± SEM). Data are expressed as percent of subsets per number live PBMC from the fresh samples and after cryopreservation for 7 days at −80°C (Gibco and the custom freezing medium). NS using Kruskall-Wallis test.
PBMC phenotype | Proposed Function | Fresh Sample | Cryopreserved with Gibco medium | Cryopreserved with the custom medium | Kruskall-Wallis Statistics |
---|---|---|---|---|---|
CD34+CD133+VEGFR2− | “Early EPC” | 0.3 ± 0.07 | 0.3 ± 0.1 | 0.3 ± 0.2 | P<0.96 |
CD34+CD133+VEGFR2+ | “Early EPC” | 0.2 ± 0.06 | 0.09 ± 0.05 | 0.00 ± 0.00 | P<0.17 |
CD34+CD133−VEGFR2+ | “Early EPC” | 0.6 ± 0.1 | 0.5 ± 0.2 | 0.2 ± 0.02 | P<0.21 |
CD146+CD34+VEGFR2− | “Late EPC” | 1.1 ± 0.2 | 1.4 ± 0.4 | 1.6 ± 0.6 | P<0.67 |
CD146+CD34+VEGFR2+ | “Late EPC” | 0.6 ± 0.1 | 0.4 ± 0.2 | 0.3 ± 0.1 | P<0.26 |
CD146+CD34−VEGFR2+ | “EC” | 0.8 ± 0.3 | 0.6 ± 0.1 | 0.2 ± 0.1 | P<0.07 |