ZnO Nanoparticles Upregulates Adipocyte Differentiation in 3T3-L1 Cells

Biol Trace Elem Res. 2016 Mar;170(1):201-7. doi: 10.1007/s12011-015-0464-7. Epub 2015 Aug 14.

Abstract

The present study was aimed to investigate the effect of zinc oxide (ZnO) nanoparticles on 3T3-L1 cell differentiation, by quantitating peroxisome proliferators-activated receptor γ (PPARγ), CCAAT/enhancer binding protein α (C/EBPα), fatty acid binding protein 4 (FABP4), sterol regulatory element-binding transcription factor 1 (SREBP1), and serine-threonine kinase cyclin-dependent kinase 4 (cdk4), which are critical for adipogenesis. 3T3-L1 preadipocyte cells were cultured and differentiated with the standard differentiation medium. Sulforhodamine B (SRB) assay determined 3T3-L1 cell viability. ZnO nanoparticles increased the lipid accumulation in differentiated adipocytes as evidenced by Oil Red O staining. The quantitative PCR (qPCR) analysis showed that the PPARγ, FABP4, C/EBPα, and SREBP1 messenger RNA (mRNA) expression was significantly increased in the ZnO nanoparticle-treated 3T3-L1 adipocytes. Western blot analysis showed increased PPARγ, FABP4, C/EBPα, and SREBP1 protein expression compared to their respective controls. Also, the immunofluorescence study showed the increased cdk4 and PPARγ expression in the nanoparticle-treated cells. Taking all these data together, it is concluded that ZnO nanoparticles may be a potent substance to alter 3T3-L1 preadipocyte differentiation and adipogenesis.

Keywords: 3T3-L1 cells; Differentiation; Lipid accumulation; SRB assay; ZnO nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipocytes / drug effects*
  • Animals
  • Blotting, Western
  • Cell Differentiation / drug effects*
  • Fluorescent Antibody Technique
  • Metal Nanoparticles / chemistry*
  • Mice
  • Polymerase Chain Reaction
  • RNA, Messenger / genetics
  • Zinc Oxide / chemistry*

Substances

  • RNA, Messenger
  • Zinc Oxide