Table 3.

Composition of human cell chimerism in the BM of engrafted NOD/SCID mice transplanted with FB, FBM, FL, and CB repopulating cells

Lineage phenotypeFB-SRC, %FBM-SRC, %FL-SRC, %CB-SRC, %
CD33+CD15+ 43 ± 13.8* 31.5 ± 8.2* 9 ± 2.1 11 ± 6.1 
CD33+CD15 8.1 ± 4.1 16.5 ± 8.1 12 ± 1.4 4.3 ± 3.8 
CD19+CD20+ 5.8 ± 3.9 13 ± 3.6 8.3 ± 2.6 8.9 ± 4.1 
CD19+CD20 4.8 ± 3.2* 17 ± 6.8* 53 ± 20.1 74 ± 12.1 
CD34+ 6.8 ± 3.5 6.5 ± 3.7 7.2 ± 3.3 5.6 ± 2.1 
CD34+CD38 2.4 ± 0.9* 0.2 ± 0.1 0.8 ± 0.4 0.2 ± 0.2 
Lineage phenotypeFB-SRC, %FBM-SRC, %FL-SRC, %CB-SRC, %
CD33+CD15+ 43 ± 13.8* 31.5 ± 8.2* 9 ± 2.1 11 ± 6.1 
CD33+CD15 8.1 ± 4.1 16.5 ± 8.1 12 ± 1.4 4.3 ± 3.8 
CD19+CD20+ 5.8 ± 3.9 13 ± 3.6 8.3 ± 2.6 8.9 ± 4.1 
CD19+CD20 4.8 ± 3.2* 17 ± 6.8* 53 ± 20.1 74 ± 12.1 
CD34+ 6.8 ± 3.5 6.5 ± 3.7 7.2 ± 3.3 5.6 ± 2.1 
CD34+CD38 2.4 ± 0.9* 0.2 ± 0.1 0.8 ± 0.4 0.2 ± 0.2 

Unfractionated or purified human FB, FBM, FL, and CB cells were transplanted into NOD/SCID mice, and murine BM was analyzed after 8 weeks. Human CD45+ cells were gated and analyzed for composition of myeloid (CD33 and CD15), B-lymphoid (CD19 and CD20), and primitive human subsets (CD34 and CD38). The percentage of each lineage is calculated as the mean ± SEM of human cells and was compared between mice transplanted with FB-SRC, FBM-SRC, FL-SRC, or CB-SRC. Data were analyzed by the unpaired, two-tailed Student t test assuming a Gaussian distribution (parametric test) and demonstrated differences as indicated (*); P < .001, n = 3-8.

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