实用肝脏病杂志 ›› 2021, Vol. 24 ›› Issue (6): 795-798.doi: 10.3969/j.issn.1672-5069.2021.06.007

• 实验性肝炎 • 上一篇    下一篇

CDE饮食诱导慢性肝损伤小鼠肝组织YAP信号对肝祖细胞增殖的影响*

沈镇扬, 王俊俊, 陆伦根, 蔡晓波   

  1. 200080 上海市 上海交通大学附属第一人民医院消化科
  • 收稿日期:2020-11-10 出版日期:2021-11-10 发布日期:2021-11-15
  • 通讯作者: 蔡晓波, E-mail: caixiaobo19790719@126.com
  • 作者简介:沈镇扬,男,25岁,硕士研究生。主要从事肝再生与非酒精性脂肪性肝病相关研究。E-mail: szycheerup@163.com
  • 基金资助:
    *国家新药开发重大科技专项基金资助项目(编号:2018ZX09201016)

Impact of YAP signal on proliferation of liver progenitor cells in mice with CDE diet-induced chronic liver injury

Shen Zhenyang, Wang Junjun, Lu Lungen, et al   

  1. Department of Gastroenterology, General Hospital, Jiaotong University School of Medicine, Shanghai 200080, China
  • Received:2020-11-10 Online:2021-11-10 Published:2021-11-15

摘要: 目的 探讨Yes相关蛋白(YAP)信号对胆碱缺乏/乙硫氨酸补充(CDE)饮食诱导慢性肝损伤模型小鼠肝组织胆管反应的影响以及体外对肝祖细胞增殖的影响。方法 采用CDE饮食喂养雄性野生型C57BL/6J小鼠3 w,采用Western blot和qPCR法检测肝组织YAP蛋白表达和基因水平;采用免疫组化法检测肝组织CK19表达,观察胆管反应程度;采用免疫荧光评估胆管反应细胞过程中YAP表达;采用两步灌注法分离原代肝祖细胞,以慢病毒感染肝祖细胞,将细胞分为YAP过表达(YAP-OE组)、过表达空载体(OE-control组)、YAP敲减(shYAP组)和敲减空载体(sh-control组),采用Western blot法检测肝组织YAP表达,采用CCK8和EdU实验评估YAP对肝祖细胞增殖能力的影响。结果 CDE造模组肝组织YAP蛋白表达比对照组增强,其YAP mRNA水平比对照组提高了2.45倍(P<0.01);CDE造模组肝组织胆管反应程度和肝祖细胞YAP表达显著高于对照组;EdU检测发现在相同培养条件下,YAP-OE组EdU阳性细胞比例较OE-control组显著增加【分别为(0.41±0.05)和(0.25±0.06),P<0.01】,CCK8检测提示在培养72 h时YAP-OE组细胞增殖活性比OE-control组提高了1.78倍(P<0.01),而在相同培养条件下,EdU检测发现shYAP组EdU阳性细胞比例较sh-control组显著减少【分别为(0.25±0.04)和(0.13±0.02),P<0.01】,在培养72h时CCK8检测提示shYAP组细胞增殖活性较sh-control组降低了1.92倍(P<0.01)。结论 CDE饮食诱导小鼠慢性肝损伤导致肝组织胆管反应活跃的祖细胞YAP表达增强,YAP在体外能促进肝祖细胞增殖。

关键词: 肝祖细胞, Yes相关蛋白, 胆管反应, 细胞增殖, 小鼠

Abstract: Objective The aim of this experiment was to investigate the impact of yes-associated protein (YAP)signal on hepatic ductular reaction in mice with choline-deficient and ethionine-supplemented (CDE) diet-induced chronic liver injury (CLI) and YAP's effect on liver progenitor cell proliferation in vitro. Methods The male wild-type C57BL/6J mice were fed with CDE diet for 3 weeks. The Western blot and qPCR were applied to detect YAP protein and gene levels in liver tissue. The immunohistochemistry were used to detect hepatic ductular reaction, the immunofluorescence to evaluate the YAP expression in ductular reaction cells, and the two-step perfusion method was used to isolate primary liver progenitor cells. The liver progenitor cells were infected by lentivirus and were divided into YAP overexpression (YAP-OE group),overexpression empty vector(OE-control group),YAP knockdown(shYAP group), and knockdown empty vector(sh-control group). The infection efficacy was evaluated by Western blot. CCK8 and EdU experiments were applied evaluate the effects of YAP on the liver progenitor cell proliferation. Results The expression of YAP protein inliver tissues in the CDE-induced model increased greatly compared to in the control group and the YAP mRNA level increased by 2.45 times than that in the control group (P<0.01); the degree of hepatic ductular response in the CDE model and the YAP mRNA level in liver progenitor cells were higher than in the control group; the EdU test found that under the same culture conditions, the percentage of EdU positive cells in the YAP-OE group was significantly increased compared to in the OE-control group [(0.41±0.05) vs. (0.25±0.06), respectively, P<0.01]; the CCK8 detection showed that the proliferation activity of cells in the YAP-OE group was 1.78 times higher than that in the OE-control group at 72 hours of culture (P<0.01); the EdU test found that the proportion of EdU positive cells in the shYAP group was significantly lower than that in the sh-control group [(0.25±0.04) vs. (0.13±0.02), respectively, P<0.01]; the CCK8 detection indicated that the proliferation activity of cells in the shYAP group was 1.92 times lower than that in the sh-control group after 72 hours of culture (P<0.01). Conclusion The CDE diet could induce chronic liver injury in mice, which results in the increase of YAP expression in progenitor cells with active ductual response. The YAP might promote the proliferation of liver progenitor cells in vitro.

Key words: Liver progenitor cells, Yes-associated protein, Ductular reaction, Proliferation, Mice