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The static magnetic field accelerates the osteogenic differentiation and mineralization of dental pulp cells

机译:静磁场会加速牙髓细胞的成骨分化和矿化

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摘要

Dental pulp cells (DPCs) can differentiate into osteoblasts and are deemed a promising cell source for bone regeneration. Static magnetic field (SMF) stimulates osteoblast differentiation but the effect in DPCs remains unknown. The aim of this study was to investigate the effect of SMF exposure on the osteogenic differentiation and mineralization of rat DPCs in vitro. Cells were continuously exposed to SMF at 290 mT in the presence/absence of osteogenic induction [dexamethasone (Dex)/β-glycerophosphate (β-GP)]. Results showed that SMF alone did not impair the cell cycle and proliferation. On the other hand, obvious condensation in the metachromatic staining of the extracellular matrix with toluidine blue was observed for SMF-exposed cells as well as the Dex/β-GP treated cells. SMF in combination with Dex/β-GP significantly increased the mRNA expression of osteogenic genes, as well as the ALP activity and extracellular calcium concentration at the early stage, followed by obvious calcium deposits later. Besides, SMF exposure increased the activity of extracellular signal-regulated kinase 1/2 (ERK1/2) at 3 h and accelerated the mRNA expression of osteogenic transcription factor, Cbfa1, advancing its activation time from 168 to 72 h under osteogenic induction. In summary, SMF exposure in combination of Dex/β-GP induction could significantly accelerate the osteogenic differentiation and mineralization of DPCs.
机译:牙髓细胞(DPC)可以分化为成骨细胞,被认为是有希望的骨再生细胞来源。静磁场(SMF)刺激成骨细胞分化,但在DPC中的作用仍然未知。这项研究的目的是调查SMF暴露对体外大鼠DPC成骨分化和矿化的影响。在存在/不存在成骨诱导作用[地塞米松(Dex)/β-甘油磷酸(β-GP)]的情况下,将细胞连续暴露于290 mT的SMF。结果表明,仅SMF不会损害细胞周期和增殖。另一方面,对于暴露于SMF的细胞以及经Dex /β-GP处理的细胞,在甲苯胺蓝的细胞外基质的变色染色中观察到明显的缩合。 SMF结合Dex /β-GP可以显着增加成骨基因的mRNA表达,并在早期显着增加ALP活性和细胞外钙浓度,随后显着增加钙沉积。此外,SMF暴露可在3 h时增加细胞外信号调节激酶1/2(ERK1 / 2)的活性,并加速成骨转录因子Cbfa1的mRNA表达,在成骨诱导下将其激活时间从168延长至72 h。综上所述,SMF暴露与Dex /β-GP诱导结合可显着促进DPC的成骨分化和矿化。

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