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. Author manuscript; available in PMC: 2014 Oct 10.
Published in final edited form as: J Blood Disord Transfus. 2013 Sep 20;4(5):158. doi: 10.4172/2155-9864.1000158

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