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. 2024 May 29;9(7):845–864. doi: 10.1016/j.jacbts.2024.02.012

Table 2.

Cellular Origin and Size of EVs Extracted From Human Valves

Aortic Stenosis Aortic Regurgitation P Value
Leukocytes, CD11a+ 5.9 ± 1.5 (22) 4.5 ± 2 (8) 0.61
Platelets, GPIb+ 1.3 ± 0.50∗∗∗ (22) 0.18 ± 0.18 (8) <0.001
Erythrocytes, CD235a+ 1.6 ± 0.57∗∗∗ (22) 0.18 ± 0.18 (8) <0.001
ECs, CD31+ 2.4 ± 0.48 (22) 2.7 ± 0.87 (8) 0.73
Activated ECs, CD105+ 25.5 ± 3.5 (22) 26.5 ± 3.1 (8) 0.08
Size, nm 145.2 ± 3.3 (8) 149.3 ± 3.2 (7) 0.82
Prothrombinase activity, nmol/L/mg of tissue 182.3 ± 12.5 (65) 122 ± 16 (13) 0.03

Values are mean ± SEM (n). Extracellular vesicles (EVs) cell origin was determined after capture onto specific antibodies and quantification by prothrombinase assay. Data are of n = 22 (aortic stenosis), n = 8 (aortic regurgitation) for immunocapture experiments, n = 8 (aortic stenosis), n = 7 (aortic regurgitation) for EVs sizing experiments, and n = 65 (aortic stenosis), n = 13 (aortic regurgitation) for prothrombinase activity. The between-group values were compared using Student’s unpaired t-test. ∗<0.05; ∗∗∗<0.001.

ECs = endothelial cells.