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Participation of extracellular signal-regulated kinases 1/2 in osteoblast and adipocyte differentiation of mesenchymal stem cells grown on titanium surfaces

机译:细胞外信号调节激酶1/2在钛表面生长的间充质干细胞的成骨细胞和脂肪细胞分化中的参与

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摘要

Osteoblasts and adipocytes coexist in the implantation site and affect the process of titanium (Ti) osseointegration. As extracellular signal-regulated kinases 1/2 (ERK1/2) are involved in osteogenesis and adipogenesis, the aim of our study was to investigate if the effects of Ti surface topography on osteoblast and adipocyte differentiation are modulated by ERK1/2. The experiments were conducted based on the effect of the ERK1/2 inhibitor, PD98059, on mesenchymal stem cells (MSCs) grown under osteogenic and adipogenic conditions on Ti with nanotopography (Ti-Nano) or on machined Ti (Ti-Machined). The results showed that, in general, ERK1/2 inhibition favored osteoblast and adipocyte differentiation of MSCs grown on Ti-Machined. In MSCs grown on Ti-Nano, ERK1/2 inhibition upregulated the expression of alkaline phosphatase and osteocalcin and reduced extracellular matrix mineralization. In terms of adipocyte differentiation, ERK1/2 inhibition elicited similar MSC responses to Ti-Nano and Ti-Machined, upregulating gene expression of adipocyte markers without affecting lipid accumulation. Our results indicate that, under osteogenic and adipogenic conditions, the responses of MSCs to Ti surface topography in terms of osteogenesis and adipogenesis are dependent on ERK1/2. Thus, a precise modulation of ERK1/2 expression and activity induced by surface topography could be a good strategy to drive the process of implant osseointegration.
机译:成骨细胞和脂肪细胞在植入部位共存,影响钛(Ti)骨整合的过程。由于细胞外信号调节的激酶1/2(ERK1 / 2)参与骨发生和脂肪发生,我们的研究目的是研究Ti表面形貌对成骨细胞和脂肪细胞分化的影响是否通过ERK1 / 2调节。该实验是基于ERK1 / 2抑制剂,PD98059的影响,对在骨膜(Ti-NaNO)或机加工Ti(Ti加工)上的骨质发生和脂肪发生条件下生长的间充质干细胞(MSCs)的影响进行进行。结果表明,一般来说,ERK1 / 2抑制有利于在Ti加工上生长的MSCs的成骨细胞和脂肪细胞分化。在Ti-Nano的MSCs中,ERK1 / 2抑制上调了碱性磷酸酶和骨甲酸的表达和细胞外基质矿化的表达。就脂肪细胞分化而言,ERK1 / 2抑制引发了与Ti-Nano和Ti加工的类似MSC响应,上调的脂肪细胞标记物的基因表达,而不会影响脂质积累。我们的结果表明,在成骨和脂肪发生条件下,在成骨发生和脂肪发生方面,MSCs对Ti表面形貌的反应依赖于ERK1 / 2。因此,通过表面形貌诱导的ERK1 / 2表达和活性的精确调制可能是驱动植入物骨整合过程的良好策略。

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