矽肺
纳米毒理学
纳米材料
转化生长因子
纳米技术
纳米颗粒
纤维化
日冕(行星地质学)
体内
材料科学
生物物理学
化学
细胞生物学
生物
医学
病理
生物技术
天体生物学
复合材料
维纳斯
作者
Zhenzhen Wang,Chunming Wang,Shang Liu,Wei He,Lintao Wang,Jingjing Gan,Zhen Huang,Zhenheng Wang,Hai-Zhen Wei,Junfeng Zhang,Lei Dong
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-01-19
卷期号:11 (2): 1659-1672
被引量:74
标识
DOI:10.1021/acsnano.6b07461
摘要
A corona is a layer of macromolecules formed on a nanoparticle surface in vivo. It can substantially change the biological identity of nanomaterials and possibly trigger adverse responses from the body tissues. Dissecting the role of the corona in the development of a particular disease may provide profound insights for understanding toxicity of nanomaterials in general. In our present study, we explored the capability of different silica nanoparticles (SiNPs) to induce silicosis in the mouse lung and analyzed the composition of coronas formed on these particles. We found that SiNPs of certain size and surface chemistry could specifically recruit transforming growth factor β1 (TGF-β1) into their corona, which subsequently induces the development of lung fibrosis. Once embedded into the corona on SiNPs, TGF-β1 was remarkably more stable than in its free form, and its fibrosis-triggering activity was significantly prolonged. Our study meaningfully demonstrates that a specific corona component on a certain nanoparticle could initiate a particular pathogenic process in a clinically relevant disease model. Our findings may shed light on the understanding of molecular mechanisms of human health risks correlated with exposure to small-scale substances.
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