05) (Fig. 1A). Histological analyses of liver tissue sections also indicated that Gal-3−/− mice are less sensitive to Con A–induced hepatic injury (Fig. 1B). Liver tissue sections in Gal-3−/− mice showed several solitary areas of necrotic tissue characterized by standard morphologic

criteria (i.e., loss of architecture, vacuolization, karyolysis, and increased eosinophilia). The majority of hepatocytes were not affected in livers of Gal-3−/− mice. In contrast, liver tissue sections in WT mice showed widespread areas of necrosis with extensive infiltration of MNCs within liver lobules (Fig. 1Ba) and around the central veins and portal tracts (Fig. 1Ca), indicating the ongoing inflammatory process (Fig. 1B,C). Extensive liver damage in WT mice was characterized by massive coagulative necrosis and cytoplasmic swelling of Dinaciclib mw the majority of hepatocytes. Nuclear chromatin condensation was found frequently, which may indicate hepatocyte apoptosis. Consistent with those findings, the

percentage of liver tissue with necrotic damage was markedly lower in Gal-3−/− mice (Supporting Fig. 2). There was conflicting evidence of whether Gal-3 deficiency attenuates both T-helper cells (Th)1 and 2 or only Th1 activity.9, 17 We found that, after Con A injection, mice lacking endogenous Gal-3−/− had significantly lower serum levels of both Th1 and 2 cytokines, in comparison Y-27632 mouse to WT mice. Serum levels of TNFα, IFNγ, and IL-17 and -4, 8 hours after Con A injection, were significantly lower in Gal-3−/−, compared to WT, mice (TNFα, P < 0.01; IFNγ, P < 0.05; IL-17, P 上海皓元 < 0.05; IL-4, P < 0.01), whereas there was no significant difference in the level of serum IL-10 between WT and GAL-3−/− mice (Supporting Fig. 3A). Despite the fact that we found the difference in cytokine levels

between WT and Gal-3−/− mice after in vivo treatment with Con A, there was no significant difference in levels of TNFα, IFNγ, and IL-17, -4, and -10 in supernatants of in vitro Con A–stimulated splenocytes of WT and Gal-3−/− mice (Supporting Fig. 3B). After Con A injection, there was an influx of MNCs in the liver. However, the number of MNCs in livers of Gal-3−/− mice was significantly lower then in WT mice (Fig. 2). Eight hours after Con A injection, there was a decrease in the total number of liver-infiltrating lymphoid cells (e.g., CD3+, CD4+, and CD8+ T cells, CD19+ B cells, and NK1.1+ NK and NK1.1+CD3+ NKT cells) (Figs. 2-4). All differences reached the level of statistical significance (P < 0.01). Also, the number of CD11c+ DCs (P < 0.01) and CD11c+CD80+CD86+-activated DCs (P < 0.05) was lower in livers of Gal-3−/−, compared to WT, mice (Figs. 2 and 4). However, there was no significant difference in the total number of T regulatory cells (Tregs; CD4+CD25+Foxp3+) between WT and Gal-3−/− mice (Fig. 2). Also, the total number of F4/80+ macrophages was similar in livers of Gal-3 mice and WT controls (Fig. 5A).