Osteoinductive function of fucoidan on periodontal ligament stem cells: Role of PI3K/Akt and Wnt/β‐catenin signaling pathways
Background/Objectives Fucoidan has been focused as a multifunctional therapeutic uses including bone health supplements. However, the critical molecular mechanisms of fucoidan for bone therapeutic agents have not been fully understood. We investigated the osteoinductive effect of fucoidan on periodo...
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Veröffentlicht in: | Oral diseases 2022-09, Vol.28 (6), p.1628-1639 |
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Sprache: | eng |
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Zusammenfassung: | Background/Objectives
Fucoidan has been focused as a multifunctional therapeutic uses including bone health supplements. However, the critical molecular mechanisms of fucoidan for bone therapeutic agents have not been fully understood. We investigated the osteoinductive effect of fucoidan on periodontal ligament stem cells (PDLSCs) and how this polymer encouraged PDLSC osteogenesis.
Materials and Methods
Osteogenic induction of PDLSCs was processed by culturing cells with fucoidan treatment. Osteogenic differentiation of PDLSCs was verified by alkaline phosphatase (ALP) activity, matrix mineralization assay, intracellular calcium levels, and mRNA expression and protein levels of osteogenic markers.
Results
Fucoidan treatment showed higher osteogenic activity in the PDLSCs than the control groups. PDLSCs with fucoidan also presented increased levels of the phosphatidylinositol‐3‐kinase (PI3K) isoforms, p110α and p110γ compared to control cells. The phosphorylation of Akt, a PI3K downstream effector, was significantly increased at 90 min of fucoidan induction. Expression of β‐catenin, a coactivator of canonical Wnt pathways, was increased in PDLSCs with fucoidan. β‐catenin was found to link with PI3K activation during the fucoidan stimulation. When cells were blocked by PI3K inhibitor or β‐catenin‐specific siRNA, fucoidan‐induced osteogenic activity of PDLSCs was significantly attenuated.
Conclusion
These findings suggest that the fucoidan stimulates osteogenic differentiation of PDLSCs via the PI3K/Akt and Wnt/β‐catenin pathways. |
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ISSN: | 1354-523X 1601-0825 |
DOI: | 10.1111/odi.13829 |