Publication | Open Access
Down-Regulation of MiR-127 Facilitates Hepatocyte Proliferation during Rat Liver Regeneration
72
Citations
33
References
2012
Year
PathologyEpigeneticsCirrhosisHepatology FibrosisRapid MethylationLiver PhysiologyLiver RegenerationRat Liver RegenerationHepatology InflammationFibrogenesisGene ExpressionMir-127 GeneCell BiologyLiver TransplantationMicrorna DetectionDevelopmental BiologyHepatologyNatural SciencesHepatitisLiver DiseaseLiver CancerSmall RnaLiverMedicineHepatocellular Carcinoma
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.
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