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TNF-α triggers osteogenic differentiation of human dental pulp stem cells via the NF-κB signalling pathway

机译:TNF-α通过NF-κB信号通路触发人牙髓干细胞的成骨分化

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Dental pulp stem cells (DPSCs) are a type of mesenchymal stem cells (MSCs) characterised by self-renewal and multi-lineage differentiation, including chondrocytes, adipocytes, neural cells and osteoblasts, which make it an attractive choice for tissue engineering purposes. Tumour necrosis factor α (TNF-α) had the positive effect on the mineralisation of bone marrow MSCs and stromal cells derived from human adipose tissue. However, the effect of TNF-α on DPSCs is unclear. We found that TNF-α activated the NF-κB pathway during the osteogenic differentiation of DPSCs. TNF-α also increased mineralisation and the expression of bone morphogenetic protein 2 (BMP2), alkaline phosphatase (ALP), runt-related transcription factor 2 (RUNX2) and collagen type I (COL I) during this process. PDTC, an NF-κB inhibitor, blocked the osteogenic differentiation induced by TNF-α. No effect of TNF-α on proliferation of DPSCs or cell cycle was detected. In summary, TNF-α promotes mineralisation and mineralisation-related gene expression through the NF-κB signalling pathway in DPSCs, which may provide a foundation for autologous transplantation of DPSCs.
机译:牙髓干细胞(DPSC)是一种间充质干细胞(MSC),其特征是自我更新和多谱系分化,包括软骨细胞,脂肪细胞,神经细胞和成骨细胞,使其成为组织工程用途的诱人选择。肿瘤坏死因子α(TNF-α)对源自人脂肪组织的骨髓间充质干细胞和基质细胞的矿化具有积极作用。然而,尚不清楚TNF-α对DPSC的作用。我们发现,TNF-α在DPSC的成骨分化过程中激活了NF-κB通路。在此过程中,TNF-α还增加了矿化作用和骨形态发生蛋白2(BMP2),碱性磷酸酶(ALP),矮子相关转录因子2(RUNX2)和I型胶原(COL I)的表达。 NF-κB抑制剂PDTC阻断TNF-α诱导的成骨分化。未检测到TNF-α对DPSCs增殖或细胞周期的影响。综上所述,TNF-α通过NF-κB信号通路促进DPSCs的矿化和与矿化相关的基因表达,这可能为DPSCs自体移植提供基础。

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