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. 1997 Feb 3;185(3):517–530. doi: 10.1084/jem.185.3.517

Table 5.

Frequency of Pluripotential and Committed Progenitors in Mice of Different Genotypes after Infection with LCMV-WE

Genotype* Virus Cellularity‡ Colonies/femur§
CFU-S BFU-E CFU-GM CFU-Meg
CD40/0 None 13.3 ± 1.4 5,978 ± 345 3,306 ± 500 33,672 ± 690 2,085 ± 237
WE  4.4 ± 1.1 (33%)‖     639 ± 163 (11%)     566 ± 30 (17%)  7,509 ± 899 (22%)     312 ± 26 (15%)
CD80/0 None 13.8 ± 0.6 6,700 ± 379 3,956 ± 379 35,376 ± 3,790 2,756 ± 152
WE  3.7 ± 1.3 (27%)     569 ± 148 (8%)     888 ± 140 (22%)  9,562 ± 984 (27%)     634 ± 15 (23%)
P0/0 None 15.3 ± 1.3 7,452 ± 916 3,263 ± 33 27,356 ± 1,498 2,825 ± 162
WE  3.7 ± 0.5 (24%)     667 ± 224 (9%)     796 ± 111 (24%)  7,712 ± 316 (28%)     565 ± 56 (20%)
lpr None 19.5 ± 2.6 ND 3,728 ± 247 28,302 ± 2,860 2,527 ± 188
WE  7.0 ± 1.5 (35%) ND     559 ± 28 (15%)  5,377 ± 524 (19%)     430 ± 37 (17%)
*

 Sex-matched 10–12-wk-old C57BL/6 mice of the indicated genotypes were infected with LCMV-WE (2 × 106 PFU) or left untreated.  

‡

 BM cellularity ×106/femur.  

§

 BM cells were harvested 3 d after infection and colony-forming cells per femur were determined in methylcellulose cultures containing IL-3 and erythropoietin (BFU-E), IL-3 and GM-CSF (CFU-GM), or IL-3 and thrombopoietin (CFU-Meg). CFU-S were counted on the spleen surface of lethally irradiated LCMV-immune C57BL/6 mice reconstituted with BM from infected or control mice. Shown are combined data from duplicate cultures of three mice tested individually.  

‖

 Data represent means ± SD, values in brackets are relative numbers of cells/colonies compared with uninfected control mice of the same genotype.