Multi-hierarchical profiling the structure-activity relationships of engineered nanomaterials at nano-bio interfaces

被引:72
作者
Cai, Xiaoming [1 ]
Dong, Jun [2 ]
Liu, Jing [3 ]
Zheng, Huizhen [1 ]
Kaweeteerawat, Chitrada [4 ]
Wang, Fangjun [3 ]
Ji, Zhaoxia [5 ,6 ]
Li, Ruibin [1 ]
机构
[1] Soochow Univ, State Key Lab Radiat Med & Protect, Sch Publ Hlth,Sch Radiat Med & Protect, Collaborat Innovat Ctr Radiol Med,Jiangsu Higher, Suzhou 215123, Jiangsu, Peoples R China
[2] Wuhan Acad Agr Sci, Wuhan 430000, Hubei, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Natl Chromatog R&A Ctr, CAS Key Lab Separat Sci Analyt Chem, Dalian 116023, Peoples R China
[4] NSTDA, Natl Nanotechnol Ctr NANOTEC, Klong Nueng 12120, Thailand
[5] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA 90095 USA
[6] Living Proof Inc, Cambridge, MA 02142 USA
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
基金
中国国家自然科学基金;
关键词
OXIDE NANOPARTICLES; OXIDATIVE STRESS; BAND-GAP; IN-VITRO; PROTEIN; CELLS; TOXICITY; SPECTROSCOPY; INTEGRATION; MIGRATION;
D O I
10.1038/s41467-018-06869-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Increasing concerns over the possible risks of nanotechnology necessitates breakthroughs in structure-activity relationship (SAR) analyses of engineered nanomaterials (ENMs) at nano-bio interfaces. However, current nano-SARs are often based on univariate assessments and fail to provide tiered views on ENM-induced bio-effects. Here we report a multi-hierarchical nano-SAR assessment for a representative ENM, Fe2O3, by metabolomics and proteomics analyses. The established nano-SAR profile allows the visualizing of the contributions of seven basic properties of Fe2O3 to its diverse bio-effects. For instance, although surface reactivity is responsible for Fe2O3-induced cell migration, the inflammatory effects of Fe2O3 are determined by aspect ratio (nanorods) or surface reactivity (nanoplates). These nano-SARs are examined in THP-1 cells and animal lungs, which allow us to decipher the detailed mechanisms including NLRP3 inflammasome pathway and monocyte chemoattractant protein-1-dependent signaling. This study provides more insights for nano-SARs, and may facilitate the tailored design of ENMs to render them desired bio-effects.
引用
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页数:12
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