Wnt信号通路
SMAD公司
干细胞
诺金
丹麦克朗
细胞生物学
化学
免疫印迹
骨形态发生蛋白2
骨形态发生蛋白
运行x2
信号转导
碱性磷酸酶
生物
生物化学
酶
体外
基因
作者
Ziting Wang,Tian Tian,Leyi Chen,Chuhan Zhang,Xiao Zheng,Ni Zhong,Buling Wu,Wenan Xu
摘要
Abstract Increasing evidence suggests stem cells from human exfoliated deciduous teeth (SHEDs) serve as desirable sources of dentin regeneration. Photobiomodulation (PBM) has shown great potential in enhancing the proliferation and osteogenesis of human bone marrow mesenchymal stem cells (hBMMSCs). However, the specific role of PBM in odontogenic differentiation of SHEDs is little know, and we further investigated potential mechanism of PBM osteo/odontogenisis. A 980 nm diode laser with different energy densities of (0.5, 5, 10 J cm −2 ) in a 100‐mW continuous wave was used for irradiation every 24 h. Osteo/odontogenic differentiation of SHEDs was achieved by performing alkaline phosphatase (ALP) and alizarin red staining (ARS) and osteo/odontogenic markers were also evaluated by qRT‐PCR and western blotting. Additionally, western blot and immunohistochemical staining were performed to evaluate the levels of BMP/Smad and Wnt/β‐catenin signaling‐related proteins. We found that PBM at 5 J cm −1 increased mineral deposition and upregulated the expression of related osteo/odontogenic markers along with the elevated expression of β‐catenin and phosphorylation level of Smad1/5/9. Furthermore, Wnt signaling inhibition using DKK1 and BMP signaling inhibition using noggin inhibited PBM‐induced osteo/odontogenic marker expression when used individually or jointly. In conclusion, PBM induces the osteo/odontogenic differentiation of SHEDs through cross talk between BMP/Smad and Wnt/β‐catenin signaling pathways.
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