Bone Research Lab, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
J Cell Physiol. 2020 Nov;235(11):8293-8303. doi: 10.1002/jcp.29674. Epub 2020 Apr 2.
This study aimed to investigate if wingless-related integration site (Wnt) signaling participates in the high osteogenic potential of titanium with nanotopography (Ti-Nano). We showed that among the several components of the Wnt signaling pathway, Frizzled 6 (Fzd6) was the transcript most intensely modulated by nanotopography compared with the untreated Ti surface (Ti-Machined). Then, we investigated whether and how Fzd6 participates in the regulation of osteoblast differentiation caused by nanotopography. The Fzd6 silencing with CRISPR-Cas9 transfection in MC3T3-E1 cells induced a more pronounced inhibition of osteoblast differentiation of cells cultured on nanotopography than those cultured on Ti-Machined. The analysis of the expression of calcium-calmodulin-dependent protein kinase II and β-catenin demonstrated that Fzd6 disruption inhibited the osteoblast differentiation induced by Ti-Nano by preventing the activation of Wnt/β-catenin but not that of Wnt/Ca signaling, which is usually triggered by the receptor Fzd6. These findings elucidate the biological function of Fzd6 as a receptor that triggers Wnt/β-catenin signaling and the cellular mechanisms modulated by nanotopography during osteoblast differentiation.
本研究旨在探讨 Wnt 信号通路是否参与了具有纳米形貌的钛(Ti-Nano)的高成骨潜力。我们发现,在 Wnt 信号通路的几个组成部分中,与未经处理的 Ti 表面(Ti-Machined)相比,Frizzled 6(Fzd6)是受纳米形貌调节最强的转录本。然后,我们研究了 Fzd6 是否以及如何参与纳米形貌引起的成骨细胞分化的调节。通过 CRISPR-Cas9 转染在 MC3T3-E1 细胞中沉默 Fzd6 ,导致在纳米形貌上培养的细胞的成骨细胞分化比在 Ti-Machined 上培养的细胞受到更明显的抑制。对钙调蛋白依赖性蛋白激酶 II 和 β-连环蛋白表达的分析表明,Fzd6 破坏通过阻止 Wnt/β-连环蛋白而不是 Wnt/Ca 信号的激活来抑制 Ti-Nano 诱导的成骨细胞分化,后者通常由受体 Fzd6 触发。这些发现阐明了 Fzd6 作为触发 Wnt/β-连环蛋白信号的受体的生物学功能,以及纳米形貌在成骨细胞分化过程中调节的细胞机制。