Original Article
Expermental study on hepatic ischemia and reperfusion injury in Rag1 and Rag2/IL2rγ knockout mice
Jin Hua, Xu Hufeng, Sun Chenyang, Zhang Chunpan, Sun Guangyong, Zhang Dong
Published 2018-02-15
Cite as Int J Surg, 2018,45(2): 107-112. DOI: 10.3760/cma.j.issn.1673-4203.2018.02.010
Abstract
ObjectiveTo explore the effect of lymphocytes on the innate immune cells in Rag1 and Rag2/IL2rγ gene knockout mice after hepatic ischemia and reperfusion injury (HIRI).
MethodsC57BL/6 mice(n=10), Rag1 knockout mice (n=10) and Rag2/IL2rγ knockout mice(n=10) were respectively divided into sham group and hepatic ischemia-reperfusion injury group by simple randomization, 5 mice in each group. By using the model of hepatic ischemia-reperfusion injury in mice, changes of intrahepatic immune cells were detected by flow cytometry. Hepatic ischemia and reperfusion injury and changes of intrahepatic cell subsets were observed in immune system-deficient mice, both Rag1 and Rag2/IL2rγ knockout. Measurement data were expressed as (±s), and analyzed using independent samples t test.
ResultsFlow cytometry results showed that immune cells, including NK cells, NKT cells, CD4+ T cells, DNT cells, Kupffer cells, BMMs and neutrophils were increased after HIRI. Compared with sham group, Rag1 knockout mice displayed markedly increased proportion of Kupffer cells, BMMs and neutrophils after HIRI. And decreased serum ALT levels [from (1 776.25±219.37) U/L to (932.33±58.77) U/L, P=0.003, t=7.350] and less hepatocellular necrosis were exhibited in Rag1 knockout mice after HIRI, comparing to C57BL/6 HIRI group. In addition, increased neutrophils were still observed in Rag2/IL2rγ knockout mice after HIRI, without increased proportion of Kupffer cells and BMMs. Compared with Rag1 knockout mice, ALT levels were further decreased from (932.33 ± 58.77) U/L to (309.00 ± 163.53) U/L (P=0.002, t=6.182) in Rag2/IL2rγ knockout mice.
ConclusionBoth Rag1 and Rag2/IL2rγ knockout mice exhibite less liver injury after HIRI comparing with C57BL/6 mice, indicating that T cells and NK cells aggravate the liver injury. Moreover, T cells do not affect the recruitment of Kupffer cells, BMMs and neutrophils, but regulate the recruitment of NK cells, while NK cells contribute to the activation of Kupffer cells and BMMs, but not neutrophil influx.
Key words:
Mice, knockout; Reperfusion injury; T-lymphocytes; Killer cells, natural; Liver
Contributor Information
Jin Hua
Experimental and Translational Research Center, Beijing Friendship Hospital, Capital Medical University; Beijing Clinical Medicine Institute; Beijing Key Laboratory of Tolerance Induction and Organ Protection in Transplantation, Beijing 100050, China
Xu Hufeng
Sun Chenyang
Zhang Chunpan
Sun Guangyong
Zhang Dong