Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5506626 | Biochemical and Biophysical Research Communications | 2016 | 6 Pages |
Abstract
The present study aimed to investigate miR-590-3p's role in osteogenic differentiation of human mesenchymal stem cells (hMSC). HMSC were cultured and transfected with empty vector, miR-590-3p vector to construct control hMSC and miR-590-3p overexpression hMSC. MiR-590-3p suppressed hMSC was created with oligonucleotide transient transfection. All 3 groups of cells were analyzed for their osteogenic level as well as Wnt/β-catenin signaling pathway activities. The results of alizarin red staining indicated that overexpression of miR-590-3p significantly enhanced mineralized deposition. Osteogenic markers including ALP, OC and SOST were also up-regulated. The result of dual-luciferase and western blot analysis indicated that miR-590-3p bound to 3â²UTR of APC mRNA selectively. By suppressing mRNA level of APC, over-expressed miR-590-3p stabilized β-catenin and increased the transcription activities of downstream target genes. These result suggested that miR-590-3p can promote osteogenic differentiation via suppressing APC expression and stabilizing β-catenin.
Keywords
CPCGSK3βhMSCRIPAAPCqRT-PCRHCOARSGAPDHCK1αmicro RNAadenomatous polyposis coliALPAlkaline phosphataseOsteocalcinOsteogenic differentiationmicroRNAsStem cellshuman mesenchymal stem cellsradioimmunoprecipitation assayUntranslated regionsUTR یا untranslated regions Tissue engineeringMiRNAHexadecylpyridinium chloridereal-time quantitative reverse transcription polymerase chain reactionoptical densityglyceraldehyde-3-phosphate dehydrogenaseGlycogen synthase kinase 3β
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Authors
Siyuan Wu, Weizhen Liu, Lei Zhou,