Exosomes Derived from Human Umbilical Cord Mesenchymal Stem Cells Enhance the Osteoblastic Differentiation of Periodontal Ligament Stem Cells Under High Glucose Conditions Through the PI3K/AKT Signaling Pathway

被引:0
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作者
YANG Shuo [1 ]
ZHU Biao [2 ]
TIAN Xiao Yu [1 ]
YU Han Ying [1 ]
QIAO Bo [1 ]
ZHAO Li Sheng [1 ]
ZHANG Bin [1 ]
机构
[1] Department of Stomatology, The First Medical Center, Chinese PLA General Hospital
[2] Department of Stomatology, Fuxing Hospital, Capital Medical University
关键词
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中图分类号
R587.2 [糖尿病性昏迷及其他并发症]; R781.42 [];
学科分类号
1002 ; 100201 ; 100302 ;
摘要
Objective High glucose(HG) can influence the osteogenic differentiation ability of periodontal ligament stem cells(PDLSCs). Human umbilical cord mesenchymal stem cell-derived exosomes(hUCMSC-exo) have broad application prospects in tissue healing. The current study aimed to explore whether hUCMSC-exo could promote the osteogenic differentiation of hPDLSCs under HG conditions and the underlying mechanism.Methods We used a 30 mmol/L glucose concentration to simulate HG conditions. CCK-8 assay was performed to evaluate the effect of hUCMSC-exo on the proliferation of hPDLSCs. Alkaline phosphatase(ALP) staining, ALP activity, and qRT-PCR were performed to evaluate the pro-osteogenic effect of hUCMSC-exo on hPDLSCs. Western blot analysis was conducted to evaluate the underlying mechanism.Results The results of the CCK-8 assay, ALP staining, ALP activity, and qRT-PCR assay showed that hUCMSC-exo significantly promoted cell proliferation and osteogenic differentiation in a dosedependent manner. The Western blot results revealed that hUCMSC-exo significantly increased the levels of p-PI3K and p-AKT in cells, and the effect was inhibited by LY294002(PI3K inhibitor) or MK2206(AKT inhibitor), respectively. Moreover, the increases in osteogenic indicators induced by hUCMSC-exo were significantly suppressed by LY294002 and MK2206.Conclusion hUCMSC-exo promote the osteogenic differentiation of hPDLSCs under HG conditions through the PI3K/AKT signaling pathway.
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页码:811 / 820
页数:10
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