An intronic miRNA regulates expression of the human endothelial nitric oxide synthase gene and proliferation of endothelial cells by a mechanism related to the transcription factor SP-1

PLoS One. 2013 Aug 5;8(8):e70658. doi: 10.1371/journal.pone.0070658. Print 2013.

Abstract

Objective: This study was to investigate the molecular mechanisms underlying the 27nt-miRNA-mediated regulation of expression of the endothelial nitric oxide synthase (eNOS) gene.

Methods: Cell lines overexpressing 27nt-miRNA or its mutant were established by transfecting the miRNA expression vector into the endothelial cells. eNOS mRNA and protein expression were examined by RT-PCR and Western Blotting, respectively. Luciferase activity reporter system was used to study the target of 27nt-miRNA.

Results: The results showed that overexpression of 27nt-miRNA significantly inhibited eNOS mRNA level and protein expression, and reduced the eNOS transcriptional efficiency. Such inhibitory effects of 27nt-miRNA were attenuated by the sequence mutations in 27nt-miRNA. Interestingly, the transcription factor SP-1 expression was reduced by 27nt-miRNA. Meanwhile, overxpression of SP-1 protein partially restored eNOS expression, and rescued the 27nt-miRNA-mediated reduction of endothelial cell proliferation. Moreover, certain sites in the SP-1 mRNA were found to be the direct target of 27nt-miRNA by a luciferase reporter system.

Conclusions: These results demonstrate that the 27nt-miRNA suppresses eNOS gene expression and SP-1 expression in vascular endothelial cells. The 27nt-miRNA directly target to SP-1 mRNA, thereby contributing to proliferation of endothelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aorta / cytology
  • Cell Proliferation*
  • Cells, Cultured
  • Endothelial Cells / enzymology*
  • Endothelial Cells / physiology
  • Endothelium, Vascular / cytology
  • Enzyme Repression
  • Gene Expression
  • Humans
  • Introns
  • MicroRNAs / genetics*
  • Nitric Oxide Synthase Type III / genetics*
  • RNA Interference
  • Sp1 Transcription Factor / genetics*
  • Sp1 Transcription Factor / metabolism

Substances

  • MicroRNAs
  • Sp1 Transcription Factor
  • NOS3 protein, human
  • Nitric Oxide Synthase Type III

Grants and funding

This work was supported by National Natural Science Foundation of China (Projects No. 30670834, and No. 30871186), and Research Foundation of the Education Department of Hunan Province, China (project No. 06A060). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.