Nigo et al. 10.1073/pnas.0510685103. |
Supporting Figure 5
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Supporting Figure 5
Fig. 5. A representative photographic view of the bronchoalveolar lavage (BAL) fluid in each group shown in Fig. 1A. Wild type (+/+) (ad) and W/Wv mice (eh) were used. Arrows indicate eosinophils, determined by characteristic morphology.
Fig. 6. Wild type (+/+) and W/Wv mice were treated and challenged as in Fig. 1, and transcriptional levels of IL-4, IL-5, IL-13, and Eotxin-2 in the BAL fluid cells were determined by real-time RT-PCR analysis.
Fig. 7. Sections shown are representative of 10 lung sections per mouse from three mice in each group shown in Fig. 1B and are with hematoxylin and eosin (H.E.) staining; magnification, ´200.
Fig. 8. Sections shown are representative of 10 lung sections per mouse from three mice in each group shown in Fig. 1B and are with Luna staining; magnification, ´400. Arrows indicate eosinophils, determined by characteristic orange staining.
Fig. 9. Sections shown are representative of 10 lung sections per mouse from three mice in each group shown in Fig. 1B. The thickness (mm) of subepithelial fibrosis was as follows: 4.5 ± 0.7 (a), 3.0 ± 0.3 (b), 5.1 ± 1.3 (c), 9.9 ± 0.6 (d), 5.0 ± 1.1 (e), 5.1 ± 2.8 (f), 5.1 ± 1.3 (g), and 6.7 ± 1.0 (h).
Fig. 10. A representative staining pattern of cells in BAL fluid of Fig. 2A. W/Wv mice (ad) and W/Wv mice reconstituted with wild type (+/+) BMMCs (eh) were immunized with PBS (a and e), LPS (b and f), OVA (c and g), and OVA plus LPS (d and h). MayGiemsa stain; magnification, ×400.
Fig. 11. A representative staining pattern of cells in BAL fluid in each group shown in Fig. 2C with MayGiemsa stain; magnification, ´400.
Fig. 12. A representative staining pattern of cells in BAL fluid in each group shown in Fig. 2D with MayGiemsa stain; magnification, ´400.
Fig. 13. A representative staining pattern of cells in BAL fluid in each group shown in Fig. 2E with MayGiemsa stain; magnification, ´400.