Utah Center for Nanomedicine, Nano Institute of Utah, University of Utah, Salt Lake City, UT 84112, USA; Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
Utah Center for Nanomedicine, Nano Institute of Utah, University of Utah, Salt Lake City, UT 84112, USA; Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT 84112, USA.
Nanomedicine. 2019 Oct;21:102041. doi: 10.1016/j.nano.2019.102041. Epub 2019 Jun 20.
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.
关于巨噬细胞在暴露时间、浓度和纳米材料物理化学性质变化时的基因表达调控,目前的可用信息有限。在这项研究中,使用不同孵育时间和浓度的球形无孔和介孔二氧化硅纳米颗粒处理 RAW264.7 巨噬细胞。使用 RNA 测序来研究转录谱。生物信息学分析、功能注释聚类和网络分析用于了解作为孔隙率、孵育时间和浓度函数的细胞反应的信号通路。在等毒性浓度和孵育时间下,孔隙率对巨噬细胞的基因组反应产生了巨大的变化。观察到时间和浓度的增加与差异表达基因数量的增加之间存在直接关系。