Table 1.

Cell No (×105) in primary lymphoid organs of RAG2/γc chimeras reconstituted with W/W or wt FL cells

Genotype of Fetal Liver Thymus Cells Bone Marrow Cells
Total LymphocytesTotal Lymphocytes NK1+CD3Pre-B Mature B
Nonreconstituted (n = 4)  0.4 ± 0.1 ND  72 ± 3  3.6 ± 1.7 ND  ND  ND  
wt (n = 7) 452 ± 94  398 ± 94  106 ± 15  26 ± 5 0.31 ± 0.15  6.12 ± 2.2  11.9 ± 1.6  
W/W (n = 7)  39 ± 24* 32 ± 23* 108 ± 8 23 ± 5  0.13 ± 0.04* 4.72 ± 1.0 8.4 ± 1.9 
Genotype of Fetal Liver Thymus Cells Bone Marrow Cells
Total LymphocytesTotal Lymphocytes NK1+CD3Pre-B Mature B
Nonreconstituted (n = 4)  0.4 ± 0.1 ND  72 ± 3  3.6 ± 1.7 ND  ND  ND  
wt (n = 7) 452 ± 94  398 ± 94  106 ± 15  26 ± 5 0.31 ± 0.15  6.12 ± 2.2  11.9 ± 1.6  
W/W (n = 7)  39 ± 24* 32 ± 23* 108 ± 8 23 ± 5  0.13 ± 0.04* 4.72 ± 1.0 8.4 ± 1.9 

Eight to ten weeks posttransfer, thymus and BM (one femur) cells of transplanted mice and control nonreconstituted RAG2/γcchimeras were enumerated and stained with a combination of either α-CD8FITC and α-CD4TRIC, α-CD3FITC and α-NK1.1PE, or α-CD19FITC and α-IgMPE mAbs. Lymphoid gates were set based on forward and side scatter parameters, and the absolute numbers were calculated as follows: total cell No × percent of lymphoid cells × percent of cells stained positive for a given marker. Pre-B cells were defined as CD19+IgM, and mature B cells were defined as CD19+ IgM+.

ND indicates not detected.

*

Indicates P < .05 for W/W versus wt chimeras.

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