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Down-Regulation of MiR-127 Facilitates Hepatocyte Proliferation during Rat Liver Regeneration

机译:MiR-127的下调促进大鼠肝再生过程中的肝细胞增殖。

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摘要

Liver regeneration (LR) after partial hepatectomy (PH) involves the proliferation and apoptosis of hepatocytes, and microRNAs have been shown to post-transcriptionally regulate genes involved in the regulation of these processes. To explore the role of miR-127 during LR, the expression patterns of miR-127 and its related proteins were investigated. MiR-127 was introduced into a rat liver cell line to examine its effects on the potential target genes Bcl6 and Setd8, and functional studies were undertaken. We discovered that miR-127 was down-regulated and inversely correlated with the expression of Bcl6 and Setd8 at 24 hours after PH, a time at which hypermethylation of the promoter region of the miR-127 gene was detected. Furthermore, in BRL-3A rat liver cells, we observed that overexpression of miR-127 significantly suppressed cell growth and directly inhibited the expression of Bcl6 and Setd8. The results suggest that down-regulation of miR-127 may be due to the rapid methylation of its promoter during the first 24 h after PH, and this event facilitates hepatocyte proliferation by releasing Bcl6 and Setd8. These findings support a miRNA-mediated negative regulation pattern in LR and implicate an anti-proliferative role for miR-127 in liver cells.
机译:部分肝切除术(PH)后的肝再生(LR)涉及肝细胞的增殖和凋亡,并且microRNA已显示出转录后调控参与这些过程调控的基因。为了探索miR-127在LR中的作用,研究了miR-127及其相关蛋白的表达模式。将MiR-127引入大鼠肝细胞系以检查其对潜在靶基因Bcl6和Setd8的影响,并进行了功能研究。我们发现,在PH后24小时(检测到miR-127基因的启动子区域甲基化的时候),miR-127被下调并且与Bcl6和Setd8的表达呈负相关。此外,在BRL-3A大鼠肝细胞中,我们观察到miR-127的过表达显着抑制细胞生长,并直接抑制Bcl6和Setd8的表达。结果表明,miR-127的下调可能是由于其启动子在PH后的最初24小时内快速甲基化,并且该事件通过释放Bcl6和Setd8促进了肝细胞的增殖。这些发现支持了LR中miRNA介导的负调控模式,并暗示了miR-127在肝细胞中的抗增殖作用。

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