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卷曲蛋白 6 缺失通过经典 Wnt 信号通路抑制纳米形貌诱导的成骨细胞分化。

Frizzled 6 disruption suppresses osteoblast differentiation induced by nanotopography through the canonical Wnt signaling pathway.

机构信息

Bone Research Lab, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

出版信息

J Cell Physiol. 2020 Nov;235(11):8293-8303. doi: 10.1002/jcp.29674. Epub 2020 Apr 2.

Abstract

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.

摘要

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。

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