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A genomic characterization of the influence of silver nanoparticles on bone differentiation in MC3T3-E1 cells.
Qing, Tao; Mahmood, Meena; Zheng, Yuanting; Biris, Alexandru S; Shi, Leming; Casciano, Daniel A.
Affiliation
  • Qing T; Center for Pharmacogenomics, School of Life Sciences and Shanghai Cancer Center, Fudan University, Shanghai, 200438, China.
  • Mahmood M; Center for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, 72204, USA.
  • Zheng Y; Center for Pharmacogenomics, School of Life Sciences and Shanghai Cancer Center, Fudan University, Shanghai, 200438, China.
  • Biris AS; Center for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, 72204, USA.
  • Shi L; Center for Pharmacogenomics, School of Life Sciences and Shanghai Cancer Center, Fudan University, Shanghai, 200438, China.
  • Casciano DA; Center for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, 72204, USA.
J Appl Toxicol ; 38(2): 172-179, 2018 Feb.
Article in En | MEDLINE | ID: mdl-28975650
ABSTRACT
Silver nanoparticles (AgNPs) have been widely used in a variety of biomedical applications. Previous studies demonstrated that AgNPs significantly enhanced bone cell mineralization and differentiation in MC3T3-1 cells, a model in vitro system, when compared to several other NPs. This increased bone deposition was evaluated by phenotypic measurements and assessment of the expression of miRNAs associated with regulation of bone morphogenic proteins. In the present study, we used RNA-seq technology, a more direct measurement of gene expression, to investigate further the mechanisms of bone differentiation induced by AgNP treatment. Key factors associated with the osteoclast pathway were significantly increased in response to AgNP exposure including Bmp4, Bmp6 and Fosl1. In addition, genes of metabolism and toxicity pathways were significantly regulated as well. Although this study suggests the potential for AgNPs to influence bone morphogenesis in injury or disease applications, further investigation into the efficacy and safety of AgNPs in bone regeneration is warranted.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoblasts / Silver / Cell Differentiation / Metal Nanoparticles / Transcriptome Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Appl Toxicol Year: 2018 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoblasts / Silver / Cell Differentiation / Metal Nanoparticles / Transcriptome Type of study: Prognostic_studies Limits: Animals Language: En Journal: J Appl Toxicol Year: 2018 Type: Article Affiliation country: China