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将氧化铈掺入中空介孔生物玻璃支架中,通过激活 ERK 信号通路增强骨再生。

Incorporation of cerium oxide in hollow mesoporous bioglass scaffolds for enhanced bone regeneration by activating the ERK signaling pathway.

机构信息

The Education Ministry Key Lab of Resource Chemistry and Shanghai Key Laboratory of Rare Earth Functional Materials, Shanghai Normal University, Shanghai 200234, People's Republic of China.

出版信息

Biofabrication. 2019 Mar 28;11(2):025012. doi: 10.1088/1758-5090/ab0676.

Abstract

Hierarchically porous structures and bioactive compositions of artificial biomaterials play a positive role in bone defect healing and new bone regeneration. Herein, cerium oxide nanoparticles-modified bioglass (Ce-BG) scaffolds were firstly constructed by the incorporation of hollow mesoporous Ce-BG microspheres in CTS via a freeze-drying technology. The interconnected macropores in Ce-BG scaffolds facilitated the in-growth of bone cells/tissues from material surfaces into the interiors, while the hollow cores and mesopore shells in Ce-BG microspheres provides more active sites for bone mineralization. The cerium oxide nanoparticles in the scaffolds rapidly promoted the proliferation and osteogenic differentiation of human bone marrow-derived mesenchymal stem cells (hBMSCs), as confirmed by the up-regulation of osteogenesis-related markers such as OCN, ALP and COL-1. The enhanced osteoinductivity of Ce-BG scaffolds was mainly related to the activated ERK pathway, and it was blocked by adding a selective ERK1/2 inhibitor (SCH772984). In vivo rat cranial defect models revealed that Ce-BG scaffolds accelerated collagen deposition, osteoblast formation and bone regeneration as compared to BG scaffolds. The exciting results demonstrated that the synergistic effects between hierarchically porous structures and cerium oxide nanoparticles contributed to osteogenic ability, and hollow mesoporous Ce-BG scaffolds would be a novel platform for bone regeneration.

摘要

人工生物材料的分级多孔结构和生物活性成分对骨缺损愈合和新骨再生起着积极的作用。在此,通过冷冻干燥技术,将中空介孔 Ce-BG 微球掺入 CTS 中,首次构建了氧化铈纳米颗粒修饰的生物玻璃(Ce-BG)支架。Ce-BG 支架中的相互连通的大孔有利于骨细胞/组织从材料表面向内生长,而 Ce-BG 微球中的中空核和介孔壳为骨矿化提供了更多的活性位点。支架中的氧化铈纳米颗粒迅速促进了人骨髓间充质干细胞(hBMSCs)的增殖和成骨分化,这一点通过上调成骨相关标志物(如 OCN、ALP 和 COL-1)得到了证实。Ce-BG 支架增强的成骨诱导性主要与激活的 ERK 途径有关,通过添加选择性 ERK1/2 抑制剂(SCH772984)可以阻断该途径。体内大鼠颅顶缺损模型表明,与 BG 支架相比,Ce-BG 支架加速了胶原沉积、成骨细胞形成和骨再生。令人兴奋的结果表明,分级多孔结构和氧化铈纳米颗粒之间的协同作用有助于提高成骨能力,中空介孔 Ce-BG 支架将成为骨再生的新平台。

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