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Notoginsenoside R1 Promotes Proliferation and Osteogenic Differentiation of hPDLSCs via Wnt/β-Catenin Signaling Pathway
by
Li, Hongkun
, Zou, Jinghua
, Yang, Yanran
, Zhang, Lina
, Han, Ruiqi
, Zhang, Wenjuan
, Zhang, Jun
in
Alizarin
/ Alkaline phosphatase
/ Antigens
/ beta Catenin - metabolism
/ Cbfa-1 protein
/ CD34 antigen
/ CD45 antigen
/ Cell adhesion & migration
/ Cell Differentiation
/ Cell Proliferation
/ Cells, Cultured
/ Cholecystokinin
/ Collagen (type I)
/ Core Binding Factor Alpha 1 Subunit - metabolism
/ Core Binding Factor Alpha 1 Subunit - pharmacology
/ Differentiation (biology)
/ Disease
/ Experiments
/ Flow cytometry
/ hpdlscs;osteogenic differentiation;wnt/β-catenin signaling pathway
/ Humans
/ Laboratories
/ Mineralization
/ ng-r1;human periodontal ligament stem cells
/ notoginsenoside r1
/ Original Research
/ Osteogenesis
/ Periodontal Ligament
/ Phosphatase
/ Signal transduction
/ Signaling
/ Stem Cells
/ Surface antigens
/ Tissue engineering
/ Tooth root
/ Wnt protein
/ Wnt Signaling Pathway
/ β-Catenin
2022
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Notoginsenoside R1 Promotes Proliferation and Osteogenic Differentiation of hPDLSCs via Wnt/β-Catenin Signaling Pathway
by
Li, Hongkun
, Zou, Jinghua
, Yang, Yanran
, Zhang, Lina
, Han, Ruiqi
, Zhang, Wenjuan
, Zhang, Jun
in
Alizarin
/ Alkaline phosphatase
/ Antigens
/ beta Catenin - metabolism
/ Cbfa-1 protein
/ CD34 antigen
/ CD45 antigen
/ Cell adhesion & migration
/ Cell Differentiation
/ Cell Proliferation
/ Cells, Cultured
/ Cholecystokinin
/ Collagen (type I)
/ Core Binding Factor Alpha 1 Subunit - metabolism
/ Core Binding Factor Alpha 1 Subunit - pharmacology
/ Differentiation (biology)
/ Disease
/ Experiments
/ Flow cytometry
/ hpdlscs;osteogenic differentiation;wnt/β-catenin signaling pathway
/ Humans
/ Laboratories
/ Mineralization
/ ng-r1;human periodontal ligament stem cells
/ notoginsenoside r1
/ Original Research
/ Osteogenesis
/ Periodontal Ligament
/ Phosphatase
/ Signal transduction
/ Signaling
/ Stem Cells
/ Surface antigens
/ Tissue engineering
/ Tooth root
/ Wnt protein
/ Wnt Signaling Pathway
/ β-Catenin
2022
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Notoginsenoside R1 Promotes Proliferation and Osteogenic Differentiation of hPDLSCs via Wnt/β-Catenin Signaling Pathway
by
Li, Hongkun
, Zou, Jinghua
, Yang, Yanran
, Zhang, Lina
, Han, Ruiqi
, Zhang, Wenjuan
, Zhang, Jun
in
Alizarin
/ Alkaline phosphatase
/ Antigens
/ beta Catenin - metabolism
/ Cbfa-1 protein
/ CD34 antigen
/ CD45 antigen
/ Cell adhesion & migration
/ Cell Differentiation
/ Cell Proliferation
/ Cells, Cultured
/ Cholecystokinin
/ Collagen (type I)
/ Core Binding Factor Alpha 1 Subunit - metabolism
/ Core Binding Factor Alpha 1 Subunit - pharmacology
/ Differentiation (biology)
/ Disease
/ Experiments
/ Flow cytometry
/ hpdlscs;osteogenic differentiation;wnt/β-catenin signaling pathway
/ Humans
/ Laboratories
/ Mineralization
/ ng-r1;human periodontal ligament stem cells
/ notoginsenoside r1
/ Original Research
/ Osteogenesis
/ Periodontal Ligament
/ Phosphatase
/ Signal transduction
/ Signaling
/ Stem Cells
/ Surface antigens
/ Tissue engineering
/ Tooth root
/ Wnt protein
/ Wnt Signaling Pathway
/ β-Catenin
2022
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Notoginsenoside R1 Promotes Proliferation and Osteogenic Differentiation of hPDLSCs via Wnt/β-Catenin Signaling Pathway
Journal Article
Notoginsenoside R1 Promotes Proliferation and Osteogenic Differentiation of hPDLSCs via Wnt/β-Catenin Signaling Pathway
2022
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Overview
To investigate the roles of Notoginsenoside R1 (NG-R1) on the proliferation and osteogenic differentiation of human periodontal ligament stem cells (hPDLSCs) and explore its possible mechanism.
hPDLSCs were isolated and, then characterized by flow cytometry. Cell-counting kit-8 (CCK-8) and colony assays were used to validate the effect of different NG-R1 concentrations on hPDLSCs proliferation and the optimal concentration was determined. Quantitative detection of alkaline phosphatase (ALP) activity at optimal concentration and the mineralization of the cells was investigated by Alizarin Red S staining. qRT-PCR and Western blot were utilized to examine the factors expression levels of ALP, Runx Family Transcription Factor 2 (RUNX2), Collagen I (Col-1) and catenin beta 1 (CTNNB1; β-catenin). In addition, the tankyrase inhibitor XAV-939 was used to explore NG-R1's role in canonical Wnt signaling.
hPDLSCs were positive for surface antigens CD90 while negative for CD34 and CD45, which indicated that we have successfully isolated the hPDLSCs. Furthermore, a concentration of 20μmol NG-R1 dramatically enhanced hPDLSCs proliferation, ALP activity, and mineral deposition. ALP, RUNX2, COL-1, and β-catenin expression were all rised in comparison to control group. After XAV-939 was added to disrupt the canonical Wnt signaling, the impact of NG-R1 appeared to be reversed.
These findings suggest that NG-R1 can stimulate osteogenic differentiation of hPDLSCs, which is probably attributable to canonical Wnt signaling activation.
Publisher
Taylor & Francis Ltd,Dove,Dove Medical Press
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