Chinese Journal of Tissue Engineering Research ›› 2019, Vol. 23 ›› Issue (17): 2625-2629.doi: 10.3969/j.issn.2095-4344.1683

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Intravenous administration of bone marrow mesenchymal stem cells protects liver function following fatty liver transplantation from donors after cardiac death

Cai Qiucheng, Fan Hongkai, Xiong Rihui, Jiang Yi   

  1. Department of Hepatobiliary Surgery, the 900th Hospital of PLA Joint Service Support Force, Fuzhou 350025, Fujian Province, China
  • Revised:2019-01-15 Online:2019-06-18 Published:2019-06-18
  • Contact: Jiang Yi, MD, Chief physician, Department of Hepatobiliary Surgery, the 900th Hospital of PLA Joint Service Support Force, Fuzhou 350025, Fujian Province, China
  • About author:Cai Qiucheng, MD, Attending physician, Department of Hepatobiliary Surgery, the 900th Hospital of PLA Joint Service Support Force, Fuzhou 350025, Fujian Province, China
  • Supported by:

    the Natural Science Foundation of Fujian Province (General Program), No. 2016J01585 (to CQC)

Abstract:

BACKGROUND: Liver transplantation from donation after cardiac death triggers a significant increase in the incidence of complications after transplantation due to the high incidence of fatty liver, long-term warm ischemia time and low perfusion time. Theoretically, mesenchymal stem cells can promote the regeneration of transplanted organ cells, and reduce ischemia-reperfusion injury as well as various immune damages after organ transplantation, thus protecting the function of transplanted organs.
OBJECTIVE: To study the effect of bone marrow mesenchymal stem cells on liver function undergoing liver transplantation from donors after cardiac death.
METHODS: Rat bone marrow mesenchymal stem cells were isolated, cultured and purified by density gradient centrifugation. The donor rats were reared to moderate-severe fatty liver, and induced cardiac death. Recipient rats were randomized into three groups: (1) control group (n=10), fatty donor liver transplantation from donation after cardiac death; (2) negative control group (n=10), fatty donor liver transplantation from donation after cardiac death plus injection of 1 mL normal saline through the portal vein; and (3) experimental group, fatty donor liver transplantation from donation after cardiac death plus injection of 1 mL PBS containing bone marrow mesenchymel stem cells (approximately 1.0×106 cells). The serum transaminase levels were evaluated at 1, 3, and 7 days after liver transplantation. Apoptosis of hepatocytes was detected using TUNEL.
RESULTS AND CONCLUSION: (1) On the 1st day after transplantation, there was no significant difference in the transaminase level among the three groups. On the 3rd and 7th days after transplantation, the levels of transaminase in the experimental group were significantly lower than those in the control group and negative control group (P < 0.05). (2) The apoptotic index of hepatocytes in the experimental group was significantly lower than that in the control group and the negative control group (P < 0.01); however, there was no significant difference between the control group and the negative control group (P > 0.05). To conclude, bone marrow mesenchymal stem cell transplantation can inhibit the apoptosis in hepatocytes and make liver function recover quickly following fatty liver transplantation from donors after cardiac death.

Key words: Cardiac death, organ transplantation, fatty liver transplantation, liver transplantation, bone marrow mesenchymal stem cells, transaminase activity, hepatocyte apoptosis, Natural Science Foundation of Fujian Province

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