Table 1.

Gene expression profiles in individual cells from defined CD34+ subpopulations circulating in neonatal cord blood

GenePeripheral blood CD34+ cell subset
CD34+CD19CD10%CD34+CD19CD10+%CD34+CD19+CD10%CD34+CD19+CD10+ %
GAPDH 97.2 (210 of 216) 98.6 (213 of 216) 100 (216 of 216) 98.6 (213 of 216) 
VpreB 0 (0 of 210) 0 (0 of 213) 58.3 (126 of 216) 54.9 (117 of 213) 
TdT 0 (0 of 210) 0 (0 of 213) 91.6 (198 of 216) 54.9 (117 of 213) 
RAG-1 0 (0 of 210) 0 (0 of 213) 37.5 (81 of 216) 38 (81 of 213) 
mb-1 3.3 (7 of 210) 19.2 (41 of 213) 51.3 (111 of 216) 53.5 (114 of 213) 
preTα 1.4 (3 of 210) 4.2 (9 of 213) 0 (0 of 216) 0 (0 of 213) 
GenePeripheral blood CD34+ cell subset
CD34+CD19CD10%CD34+CD19CD10+%CD34+CD19+CD10%CD34+CD19+CD10+ %
GAPDH 97.2 (210 of 216) 98.6 (213 of 216) 100 (216 of 216) 98.6 (213 of 216) 
VpreB 0 (0 of 210) 0 (0 of 213) 58.3 (126 of 216) 54.9 (117 of 213) 
TdT 0 (0 of 210) 0 (0 of 213) 91.6 (198 of 216) 54.9 (117 of 213) 
RAG-1 0 (0 of 210) 0 (0 of 213) 37.5 (81 of 216) 38 (81 of 213) 
mb-1 3.3 (7 of 210) 19.2 (41 of 213) 51.3 (111 of 216) 53.5 (114 of 213) 
preTα 1.4 (3 of 210) 4.2 (9 of 213) 0 (0 of 216) 0 (0 of 213) 

Indicated IgMCD34+ hemopoietic progenitor populations were purified from neonatal cord blood from 8 donors, as shown in Figure 1. The correlated expression of the gene panel, measured at the single-cell level, was performed as in Figure 2 (18-36 cells/donor). Results indicate the percentage of individual cells showing amplification of the indicated genes among the total number of single cells analyzed in each subpopulation. Only tubes showing GAPDH amplification (97.2%-100%) were considered in this study. Numbers in parentheses indicate the number of cells showing specific amplification divided by the number of GAPDH+ cells analyzed in each subset.

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