Frontiers in Pharmacology (Aug 2020)

Delivery of microRNA-33 Antagomirs by Mesoporous Silica Nanoparticles to Ameliorate Lipid Metabolic Disorders

  • Yaoye Tao,
  • Yaoye Tao,
  • Shengjun Xu,
  • Shengjun Xu,
  • Jianguo Wang,
  • Jianguo Wang,
  • Li Xu,
  • Li Xu,
  • Chenzhi Zhang,
  • Chenzhi Zhang,
  • Kangchen Chen,
  • Kangchen Chen,
  • Zhengxing Lian,
  • Zhengxing Lian,
  • Junbin Zhou,
  • Junbin Zhou,
  • Haiyang Xie,
  • Haiyang Xie,
  • Shusen Zheng,
  • Shusen Zheng,
  • Xiao Xu,
  • Xiao Xu

DOI
https://doi.org/10.3389/fphar.2020.00921
Journal volume & issue
Vol. 11

Abstract

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Lipid metabolic disorders have become a major global public health concern. Fatty liver and dyslipidemia are major manifestations of these disorders. Recently, MicroRNA-33 (miR-33), a post-transcriptional regulator of genes involved in cholesterol efflux and fatty acid oxidation, has been considered as a good therapeutic target for these disorders. However, the traditional methods of gene therapy impede their further clinical transformation into a mature treatment system. To counter this problem, in this study we used mesoporous silica nanoparticles (MSNs) as nanocarriers to deliver miR-33 antagomirs developing nanocomposites miR-MSNs. We observed that the hepatocellular uptake of miR-33 antagomirs increased by ∼5 times when they were delivered using miR-MSNs. The regulation effects of miR-MSNs on miR-33 and several genes involved in lipid metabolism were confirmed in L02 cells. In a high-fat diet fed mice, miR-33 intervention via miR-MSNs lowered the serum triglyceride levels remarkably by 18.9% and reduced hepatic steatosis. Thus, our results provide a proof-of-concept for a potential strategy to ameliorate lipid metabolic disorders.

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