IL-22 Protects against Biliary Ischemia-Reperfusion Injury after Liver Transplantation via Activating STAT3 and Reducing Apoptosis and Oxidative Stress Levels In Vitro and In Vivo

<div>IL-22 can promote cell migration and proliferation in vitro. (a and c) Compared with the CON group, the cell migration rate was significantly increased at 24 and 48 hours after IL-22 treatment. (b and d~f) Compared with the CoCl<sub>2</sub> group, the proportion of cells in the 4N phase in the CoCl<sub>2</sub>+IL-22 group was significantly increased at 24, 48, and 72 hours after IL-22 treatment. 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Oxidative Medicine and Cellular Longevity

fig3

Figure 3

Figure 3: IL-22 Protects against Biliary Ischemia-Reperfusion Injury after Liver Transplantation via Activating STAT3 and Reducing Apoptosis and Oxidative Stress Levels In Vitro and In Vivo 

Figure 3 | IL-22 Protects against Biliary Ischemia-Reperfusion Injury after Liver Transplantation via Activating STAT3 and Reducing Apoptosis and Oxidative Stress Levels In Vitro and In Vivo 