Abstract
Wnt signaling determines human stromal (mesenchymal) stem cell (hMSC) differentiation fate into the osteoblast or adipocyte lineage. microRNAs (miRNAs) are small RNA molecules of 21-25 nucleotides that regulate many aspects of osteoblast biology. Thus, we examined miRNAs regulated by Wnt signaling in hMSC. We identified miRNA (miR)-141-3p as a Wnt target which in turn inhibited Wnt signaling. Moreover, miR-141-3p inhibited hMSC proliferation by arresting cells at the G1 phase of the cell cycle. miR-141-3p inhibited osteoblast differentiation of hMSC as evidenced by reduced alkaline phosphatase activity, gene expression and in vitro mineralized matrix formation. Bioinformatic studies, Western blot analysis and 3'UTR reporter assay demonstrated that cell division cycle 25A (CDC25A) is a direct target of miR-141-3p. siRNA-mediated knock-down of CDC25A inhibited hMSC proliferation and osteoblast differentiation. In summary, miR-141-3p acts as a negative regulator of hMSC proliferation and osteoblast differentiation. Targeting miR-141-3p could be used as an anabolic therapy of low bone mass diseases, e.g. osteoporosis.
| Original language | English |
|---|---|
| Journal | BBA Molecular Cell Research |
| Volume | 1843 |
| Issue number | 9 |
| Pages (from-to) | 2114-21 |
| Number of pages | 8 |
| ISSN | 0167-4889 |
| DOIs | |
| Publication status | Published - Sept 2014 |
Keywords
- Animals
- Base Sequence
- Cell Differentiation
- Cell Proliferation
- G1 Phase Cell Cycle Checkpoints
- Gene Expression Regulation
- Gene Knockdown Techniques
- Humans
- Mesenchymal Stromal Cells
- Mice
- MicroRNAs
- Molecular Sequence Data
- Osteoblasts
- Wnt Signaling Pathway
- cdc25 Phosphatases
