miR‑488 negatively regulates osteogenic differentiation of bone marrow mesenchymal stem cells induced by psoralen by targeting Runx2
miR‑488 negatively regulates osteogenic differentiation of bone marrow mesenchymal stem cells induced by psoralen by targeting Runx2
It has been previously reported that psoralen, one of the active ingredients in Psoralea corylifolia, could induce osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs), suggesting its potential to treat osteoporosis. Additionally, runt‑related transcription factor 2 (Runx2) is a transcription factor that plays vital roles in BMSC osteogenic differentiation. However, whether and how microRNAs (miRNAs/miRs) modulate osteogenic differentiation induced by psoralen have not yet been examined, to the best of the authors' knowledge. The present study aimed to identify the miRNA target genes that regulate osteogenic differentiation of BMSCs induced by psoralen. A Cell Counting Kit‑8 assay and alizarin red staining were used to detect the viability and osteogenic differentiation of BMSCs, respectively, under treatment with psoralen. miRNA microarray analysis was performed to identify the differentially expressed miRNAs under treatment with psoralen. A bioinformatics analysis and a luciferase reporter assay were conducted to identify the targets of miR‑488. Finally, the mechanisms of miR‑488 in psoralen‑induced BMSC osteogenic differentiation were investigated using overexpression or inhibition methods in vitro. Cell viability was elevated and osteogenic differentiation of BMSCs was improved under treatment with psoralen. miRNA microarray analysis and further validation by reverse transcription‑quantitative PCR revealed that miR‑488 was downregulated during psoralen‑induced BMSC osteogenic differentiation. Bioinformatics analysis and experimental validation by a luciferase reporter assay identified Runx2 as a potential target of miR‑488. Overexpression of miR‑488 by transfection with miR‑488 mimics markedly inhibited the expression of Runx2, Osterix and alkaline phosphatase, whereas, the inhibition of miR‑488 expression by the miR‑488 inhibitor promoted their expression compared with the control. Rescue assays demonstrated that Runx2 overexpression partially rescued the inhibitory effect of miR‑488 on BMSC osteogenic differentiation. The present results suggested that miR‑488 is a negative regulator of psoralen‑induced BMSC osteogenic differentiation by targeting Runx2, providing a possible therapeutic target for osteoporosis.
- First Affiliated Hospital of Guangzhou University of Chinese Medicine China (People's Republic of)
- Guangzhou University of Chinese Medicine China (People's Republic of)
- Guangdong Provincial Hospital of Traditional Chinese Medicine China (People's Republic of)
- The Third Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine China (People's Republic of)
Male, Cell Survival, Ficusin, Cell Differentiation, Core Binding Factor Alpha 1 Subunit, Mesenchymal Stem Cells, Articles, Psoralea, Rats, Sprague-Dawley, MicroRNAs, Gene Expression Regulation, Osteogenesis, Animals, Cells, Cultured
Male, Cell Survival, Ficusin, Cell Differentiation, Core Binding Factor Alpha 1 Subunit, Mesenchymal Stem Cells, Articles, Psoralea, Rats, Sprague-Dawley, MicroRNAs, Gene Expression Regulation, Osteogenesis, Animals, Cells, Cultured
8 Research products, page 1 of 1
- 1981IsAmongTopNSimilarDocuments
- 1982IsAmongTopNSimilarDocuments
- 2000IsAmongTopNSimilarDocuments
- 2020IsAmongTopNSimilarDocuments
- 2000IsAmongTopNSimilarDocuments
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).17 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Average impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
