Time- and dose-dependent gene expression analysis of macrophage response as a function of porosity of silica nanoparticles

被引:6
|
作者
Yazdimamaghani, Mostafa [1 ,2 ]
Moos, Philip J. [1 ,3 ]
Ghandehari, Hamidreza [1 ,2 ,4 ]
机构
[1] Univ Utah, Nano Inst Utah, Utah Ctr Nanomed, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Pharmacol & Toxicol, 112 Skaggs Hall, Salt Lake City, UT 84112 USA
[4] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
关键词
Silica nanoparticles; Global gene expression; Bioinformatics; Network analysis; Signaling pathways; CELLULAR TOXICITY; OXIDATIVE STRESS; IN-VIVO; SIZE; GEOMETRY; SAFETY;
D O I
10.1016/j.nano.2019.102041
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
There is a limited amount of information available on gene expression regulation of macrophages in response to changing the time of exposure, concentration, and physicochemical properties of nanomaterials. In this study, RAW264.7 macrophages were treated with spherical nonporous and mesoporous silica nanoparticles of similar size at different incubation times and concentrations. RNA-sequencing was used to study transcriptional profiles. Bioinformatics analyses, functional annotation clustering, and network analyses were employed to understand signaling pathways of cellular response as a function of porosity, incubation time, and concentration. Porosity introduced drastic changes to the genomic response of macrophages at equitoxic concentrations and incubation times. Direct relations between increases in time and concentration with an increased number of differentially expressed genes were observed. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页数:12
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