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The induction of cellular senescence in dental follicle cells inhibits the osteogenic differentiation

机译:牙囊细胞中细胞衰老的诱导抑制成骨细胞分化

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摘要

Dental stem cells such as human dental follicle cells (DFCs) have opened new promising treatment alternatives for today's dental health issues such as periodontal tissue regeneration. However, cellular senescence represents a restricting factor to cultured stem cells, resulting in limited lifespan and reduced cell differentiation potential. Therefore, this study evaluated if and how DFCs exhibit features of cellular senescence after being expanded in cell culture. The cell proliferation of DFCs decreased, while the cell size increased during prolonged cell culture. Moreover, DFCs expressed the senescence-associated beta-galactosidase after a prolonged cell culture. The onset of senescence inhibited both the induction of osteoblast markers RUNX2 and osteopontin and the biomineralization of DFCs after stimulation of the osteogenic differentiation. In conclusion, we showed that a prolonged cell culture induces cellular senescence and inhibits the osteogenic differentiation in DFCs.
机译:诸如人牙囊细胞(DFC)等牙科干细胞为当今的牙齿健康问题(例如牙周组织再生)开辟了新的有前途的治疗替代方法。然而,细胞衰老是培养的干细胞的限制因素,导致寿命有限和细胞分化潜力降低。因此,这项研究评估了DFC在细胞培养物中扩增后是否以及如何表现出细胞衰老的特征。在长时间的细胞培养过程中,DFC的细胞增殖减少,而细胞大小增加。此外,DFCs在长时间的细胞培养后表达了与衰老相关的β-半乳糖苷酶。在刺激成骨分化后,衰老的开始既抑制了成骨细胞标记RUNX2和骨桥蛋白的诱导,也抑制了DFCs的生物矿化作用。总之,我们证明了延长的细胞培养会诱导细胞衰老并抑制DFC中的成骨分化。

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