首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Regulation of Long Non-Coding RNA-Dreh Involved in Proliferation and Migration of Hepatic Progenitor Cells during Liver Regeneration in Rats
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Regulation of Long Non-Coding RNA-Dreh Involved in Proliferation and Migration of Hepatic Progenitor Cells during Liver Regeneration in Rats

机译:大鼠肝脏再生过程中涉及肝祖细胞增殖和迁移的长非编码RNA-Dreh的调控。

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摘要

Liver regeneration plays a significant role in protecting liver function after liver injury or chronic liver disease. Long non-coding RNAs (lncRNAs) are considered to be involved in the proliferation of hepatocytes and liver regeneration. Therefore, this study aimed to explore the effects of LncRNA-Dreh on the regulation of hepatic progenitor cells (HPCs) during liver regeneration in rats. Initially, the rat model of liver injury was established to investigate the effect of LncRNA-Dreh down-regulation on liver tissues of rats with liver injury. Subsequently, HPCs line WB-F344 cells were transfected with interference plasmid of LncRNA-Dreh and the expression of LncRNA-Dreh and Vimentin was detected. The proliferation and migration ability of WB-F344 cells, as well as the content of albumin (ALB) and alpha fetoprotein (AFP) in cell differentiation were then determined. Disorderly arranged structure of liver tissue, a large number of HPCs set portal area as center extended to hepatic lobule and ductular reaction were observed in liver tissues of rats with liver injury. The expression of LncRNA-Dreh decreased while Vimentin increased in liver tissues of rats with liver injury. Moreover, the proliferation and migration ability, expression of Vimentin and AFP in WB-F344 cells were increased after silencing of LncRNA-Dreh and ALB was decreased. Collectively, our findings demonstrate that inhibition of LncRNA-Dreh can enhance the proliferation and migration abilities of HPCs in liver regeneration but cause abnormal differentiation of HPCs.
机译:在肝损伤或慢性肝病后,肝再生在保护肝功能中起重要作用。长的非编码RNA(lncRNA)被认为与肝细胞的增殖和肝脏的再生有关。因此,本研究旨在探讨LncRNA-Dreh对大鼠肝再生过程中肝祖细胞(HPCs)的调节作用。最初,建立大鼠肝损伤模型以研究LncRNA-Dreh下调对肝损伤大鼠肝组织的影响。随后,用LncRNA-Dreh的干扰质粒转染HPCs细胞系WB-F344细胞,并检测LncRNA-Dreh和波形蛋白的表达。然后测定WB-F344细胞的增殖和迁移能力,以及细胞分化中白蛋白(ALB)和甲胎蛋白(AFP)的含量。肝损伤大鼠肝脏组织中观察到肝组织结构无序排列,大量的HPC以门户区域为中心延伸至肝小叶,并发生导管反应。肝损伤大鼠肝组织中LncRNA-Dreh的表达降低,而波形蛋白增加。此外,LncRNA-Dreh沉默后,WB-F344细胞的增殖和迁移能力,波形蛋白和AFP的表达增加,ALB降低。总体而言,我们的发现表明,抑制LncRNA-Dreh可以增强HPC在肝脏再生中的增殖和迁移能力,但会引起HPC异常分化。

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