Brief Article
Copyright ©2010 Baishideng.
World J Gastroenterol. Feb 7, 2010; 16(5): 636-640
Published online Feb 7, 2010. doi: 10.3748/wjg.v16.i5.636
Figure 1
Figure 1 Reverse transcription polymerase chain reaction (RT-PCR) shows indoleamine 2,3-dioxygenase (IDO) and FasL expression in Kupffer cells (KC) before and after activation with recombinant interferon-γ (IFN-γ). RT-PCR showing FasL expression in KC before (lanes 1 and 2) and after activation for 6 h (lanes 3 and 4) or 24 h (lane 5) with IFN-γ. RT-PCR showing IDO expression in KC before (lanes 6-8) and after activation for 6 h (lane 9) or 24 h (lane 10) with IFN-γ.
Figure 2
Figure 2 Tryptophan (A) and kynurenine (B) concentration in cultures of KC. The kynurenine concentration significantly increased while tryptophan decreased in KC pretreated with IFN-γ for 24 h. aP < 0.05 vs KC group.
Figure 3
Figure 3 Reduction of allogeneic T-cell stimulation by IDO and FasL-expressing KC. Naive lymphocyte (LC), naive KC, KC pretreated with IFN-γ were coincubated with allogeneic spleen T-cell for 5 d and cell proliferation measured by 3H-TdR incorporation. aP < 0.05 vs KC group.
Figure 4
Figure 4 Anti-FasL antibody (A) or 1-methyl-tryptophan (1-MT) (B) enhances the proliferation of allogeneic T-cell stimulated with KC pretreated with IFN-γ. aP < 0.05 vs control group.
Figure 5
Figure 5 KC induces apoptosis of allogeneic T-cell. The KC pretreated with IFN-γ exhibit a significant allogeneic T-cell apoptosis. aP < 0.05 vs KC group.