Shikonin inhibits adipogenic differentiation via regulation of mir-34a-FKBP1B

Biochem Biophys Res Commun. 2015 Nov 27;467(4):941-7. doi: 10.1016/j.bbrc.2015.10.039. Epub 2015 Oct 22.

Abstract

Shikonin is a naturally occurring naphthoquinone pigment and a major constituent present in Lithospermum erythrorhizon. Since microRNAs (miRNAs) are one of the key post-transcriptional regulators of adipogenesis, their manipulation represents a potential new strategy to inhibit adipogenesis. Our aim was to investigate shikonin-dependent inhibition of adipogenesis with an emphasis on miRNA-related processes. Mir-34a increased during induced adipogenesis, and this was suppressed in the presence of shikonin. mRNA expression of FKBP1B, a suggested target of mir-34a according to bioinformatics studies, decreased during adipogenesis, but was recovered by shikonin treatment, which reversely correlated with mir-34a expression. A mir-34a inhibitor suppressed MDI-induced adipogenesis by blocking PPARγ and C/EBPα expression, while suppression of mir-34a recovered MDI-induced down-regulation of FKBP1B expression. A mir-34a mimic decreased FKBP1B mRNA expression in 3T3-L1 preadipocytes. We also observed that mir-34a bound directly to the 3'-untranslated region of FKBP1B. Finally, FKBP1B overexpression attenuated MDI-induced adipogenesis, PPARγ, and C/EBPα expression. These results suggest that mir-34a regulates adipogenesis by targeting FKBP1B expression. Our findings reveal that shikonin prevents adipogenesis by blocking the mir-34a-FKBP1B pathway which represents a promising potential target for preventing obesity.

Keywords: Adipogenesis; FKBP1B; Mir-34a; Shikonin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology
  • Adipocytes / drug effects*
  • Adipogenesis / physiology
  • Animals
  • Cell Differentiation / drug effects*
  • Mice
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / physiology*
  • Naphthoquinones / pharmacology*
  • Tacrolimus Binding Proteins / genetics
  • Tacrolimus Binding Proteins / physiology*

Substances

  • FKBP1B protein, mouse
  • MIRN34a microRNA, mouse
  • MicroRNAs
  • Naphthoquinones
  • shikonin
  • Tacrolimus Binding Proteins