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

Table 3.

BM Cytology of Wild type, IFN-α/β R0/0, and IFN-γ R0/0 Mice Infected with LCMV-WE

Genotype Days after infection* Megakaryocyte§ Cell type (%)‡
Erythroblast Myeloblast promyelocyte Myelocyte metamyelocyte band Polymorph Monocyte Lymphocyte
Wild type Uninfected 17–25    35.5 ± 1  9.5 ± 1.8 36.5 ± 2.8  7.7 ± 1.5 0.8 ± 0.3    10 ± 1.4
Wild type 3  4–11 15.5 ± 1.4 28.5 ± 1.3 37.5 ± 2.5  4.0 ± 1 <0.5 14.5 ± 2.3
IFN-α/β R0/0 3 21–26 37.5 ± 1.5 10.5 ± 0.5 33.5 ± 2.6 12.0 ± 2 1.0 ± 0.4  5.5 ± 0.1
IFN-γ R0/0 3  8–13 17.0 ± 1.8 28.5 ± 1.8 39.5 ± 3.2  3.5 ± 0.5 <0.5 11.5 ± 0.3
*

 Sex-matched mice (8–12 wk) of different genotypes (three mice per group) were infected with LCMV-WE (2 × 106 PFU). At the time points indicated, BM smears were stained with May-Günwald/Giemsa, chloracetate esterase, α-naphthyl butyrate esterase, and Sudan black B. Differential counts were obtained microscopically by counting 200 or more cells.  

‡

 Data are means ± SD of the relative number of total cells per lineage. Eosinophils were included in granulocyte counts.  

§

Numbers represent megakaryocytes per visual field at a magnification of ×80. They were determined semiquantitatively by counting at least four visual fields.