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Time- and dose-dependent gene expression analysis of macrophage response as a function of porosity of silica nanoparticles.
Yazdimamaghani, Mostafa; Moos, Philip J; Ghandehari, Hamidreza.
Affiliation
  • Yazdimamaghani M; 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.
  • Moos PJ; 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. Electronic address: philip.moos@utah.edu.
  • Ghandehari H; 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; Department of Bioengineering, University of Utah, Salt Lake City, UT 84112, USA. Electronic address: hamid.ghandehari@utah.edu.
Nanomedicine ; 21: 102041, 2019 10.
Article in En | MEDLINE | ID: mdl-31228603
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Silicon Dioxide / Nanoparticles / Macrophages Limits: Animals Language: En Journal: Nanomedicine Journal subject: BIOTECNOLOGIA Year: 2019 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Silicon Dioxide / Nanoparticles / Macrophages Limits: Animals Language: En Journal: Nanomedicine Journal subject: BIOTECNOLOGIA Year: 2019 Document type: Article Affiliation country: Country of publication: