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银纳米颗粒对 MC3T3-E1 细胞骨分化影响的基因组特征分析。

A genomic characterization of the influence of silver nanoparticles on bone differentiation in MC3T3-E1 cells.

机构信息

Center for Pharmacogenomics, School of Life Sciences and Shanghai Cancer Center, Fudan University, Shanghai, 200438, China.

Center for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, 72204, USA.

出版信息

J Appl Toxicol. 2018 Feb;38(2):172-179. doi: 10.1002/jat.3528. Epub 2017 Oct 4.

Abstract

Silver nanoparticles (AgNPs) have been widely used in a variety of biomedical applications. Previous studies demonstrated that AgNPs significantly enhanced bone cell mineralization and differentiation in MC3T3-1 cells, a model in vitro system, when compared to several other NPs. This increased bone deposition was evaluated by phenotypic measurements and assessment of the expression of miRNAs associated with regulation of bone morphogenic proteins. In the present study, we used RNA-seq technology, a more direct measurement of gene expression, to investigate further the mechanisms of bone differentiation induced by AgNP treatment. Key factors associated with the osteoclast pathway were significantly increased in response to AgNP exposure including Bmp4, Bmp6 and Fosl1. In addition, genes of metabolism and toxicity pathways were significantly regulated as well. Although this study suggests the potential for AgNPs to influence bone morphogenesis in injury or disease applications, further investigation into the efficacy and safety of AgNPs in bone regeneration is warranted.

摘要

银纳米粒子(AgNPs)已广泛应用于各种生物医学领域。先前的研究表明,与其他几种纳米粒子相比,AgNPs 可显著增强 MC3T3-1 细胞(一种体外模型系统)中的成骨细胞矿化和分化。通过表型测量和评估与骨形态发生蛋白调节相关的 miRNA 的表达来评估这种增加的骨沉积。在本研究中,我们使用 RNA-seq 技术(一种更直接的基因表达测量方法)进一步研究了 AgNP 处理诱导骨分化的机制。与破骨细胞途径相关的关键因子在 AgNP 暴露后显著增加,包括 Bmp4、Bmp6 和 Fosl1。此外,代谢和毒性途径的基因也得到了显著调节。虽然这项研究表明 AgNPs 有可能影响损伤或疾病应用中的骨形态发生,但仍需要进一步研究 AgNPs 在骨再生中的功效和安全性。

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