TABLE 2.
IFN-γ restores the hepatic iNOS and ICAM-1 responses to LPS in DEM-treated CF1 micea
Antigen | Challenge | Positive cellsb
|
||
---|---|---|---|---|
KC (cells/HPF) | Hep (cells/HPF) | EC (intensity score) | ||
TNF-α | LPS | <0.2 | — | 0 |
LPS + IFN-γ | <0.2 | — | 0 | |
iNOS | LPS | 15.4 ± 2.3 | 0.6 ± 0.9 | 1 |
LPS + IFN-γ | 17.6 ± 2.3 | 28.8 ± 4.6∗ | 2 | |
ICAM-1 | LPS | 4.0 ± 1.6 | — | 1 |
LPS + IFN-γ | 14.0 ± 4.1∗ | — | 2 | |
F4/80 | LPS | 24.6 ± 4.3 | — | 0 |
LPS + IFN-γ | 26.4 ± 3.8 | — | 0 |
CF1 mice (five per group) were injected i.p. with DEM (5.3 mmol/kg) 2 h prior to challenge. Mice were challenged i.p. with either 100 μg of E. coli O111:B4 LPS or LPS plus 2 μg of recombinant IFN-γ. Liver samples were recovered 6 h later for immunohistology and read at ×400 magnification.
See Table 1, footnotes a and b. ∗, these groups differed significantly from their controls (LPS only) (P < 0.01).