南方医科大学学报 ›› 2014, Vol. 34 ›› Issue (07): 1005-.

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重组慢病毒介导LXRα RNA干扰改善大鼠脂肪肝供肝移植术后的功能

赵英鹏,李立,马菁璠,陈刚,白建华   

  • 出版日期:2014-07-20 发布日期:2014-07-20

Lentiviral-mediated RNA interference of LXRα gene in donor rats with fatty liver
enhances liver graft function after transplantation

  • Online:2014-07-20 Published:2014-07-20

摘要: 目的探讨LXRα RNA干扰(RNAi)改善脂肪肝供肝大鼠肝移植术后肝功能的作用及机制。方法50只SD大鼠,给予高脂
饲料和56%的酒精喂养,诱导成平均脂变程度大于60%的脂肪肝作为肝移植供体。实验组25只脂肪肝供体大鼠在移植前72 h
自门静脉注射7×107 TU LXRα-RNAi的慢病毒混悬液(LXRα-RNAi-LV),对照组25只脂肪肝供体大鼠移植前72 h自门静脉接受
阴性对照慢病毒(NC-LV)载体液注射。受体大鼠均接受原位肝移植术。术后检测肝酶学、组织切片、TUNEL、细胞因子、组织
蛋白及RT-PCR水平。结果LXRα-RNAi-LV治疗组与对照组相比较,术后移植肝肝细胞内脂肪酸蓄积明显受到抑制,肝酶学及
肝组织损伤相关细胞因子水平明显下降,组织损伤较轻,大鼠平均生存率提高。RT-PCR示实验组LXRα mRNA水平明显低于
对照组,Western blotting 提示LXRα,SREBP-1c,CD36表达明显低于对照组。结论LXRα-RNAi-LV 基因治疗能明显降低LXRα
基因的表达,改善脂肪肝供肝大鼠肝移植术后肝功能、提高生存率。

Abstract: Objective To investigate whether RNA interference (RNAi) of LXRα gene in donor rats with fatty liver improves
liver graft function after transplantation. Methods Fifty donor SD rats were fed a high-fat diet and 56% alcohol to induce
macrovesicular steatosis exceeding 60% in the liver. The donor rats were injected via the portal veins with 7 × 107 TU
LXRα-RNAi-LV mixture (n=25) or negative control-LV (NC-LV) vector (n=25) 72 h before orthotopic liver transplantation. At 2,
24, and 72 h after the transplantation, the recipient rats were sacrificed to examine liver transaminases, liver graft histology,
immunostaining (TUNEL), and protein and mRNA levels of LXRα. Results Lentivirus-LXRα RNAi inhibited LXRα gene
expression at both the mRNA and protein levels in the liver graft and reduced the expressions of SREBP-1c and CD36 as
compared with the controls, resulting also in reduced fatty acid accumulation in the hepatocytes. The recipient rats receiving
RNAi-treated grafts showed more obvious reduction in serum ALT, AST, IL-1β and TNF-α levels, and exhibited milder hepatic
pathologies than the control rats after the transplantation. TUNEL assay demonstrated a significant reduction in cell apoptosis
in LXRα-RNAi-LV-treated liver grafts, and the rats receiving treated liver grafts had a prolonged mean overall survival time.
Conclusion LXRα-RNAi-LV treatment of the donor rats with fatty liver can significantly down-regulate LXRα gene expression
in the liver graft and improve the graft function and recipient rat survival after liver transplantation.