Loss of Hilnc prevents diet-induced hepatic steatosis through binding of IGF2BP2

Nat Metab. 2021 Nov;3(11):1569-1584. doi: 10.1038/s42255-021-00488-3. Epub 2021 Nov 8.

Abstract

The Hedgehog (Hh) signalling pathway plays a critical role in regulating liver lipid metabolism and related diseases. However, the underlying mechanisms are poorly understood. Here, we show that the Hh signalling pathway induces a previously undefined long non-coding RNA (Hilnc, Hedgehog signalling-induced long non-coding RNA), which controls hepatic lipid metabolism. Mutation of the Gli-binding sites in the Hilnc promoter region (HilncBM/BM) decreases the expression of Hilnc in vitro and in vivo. HilncBM/BM and Hilnc-knockout mice are resistant to diet-induced obesity and hepatic steatosis through attenuation of the peroxisome proliferator-activated receptor signalling pathway, as Hilnc directly interacts with IGF2BP2 to enhance Pparγ mRNA stability. Furthermore, we identify a potential functional human homologue of Hilnc, h-Hilnc, which has a similar function in regulating cellular lipid metabolism. These findings uncover a critical role of the Hh-Hilnc-IGF2BP2 signalling axis in lipid metabolism and suggest a potential therapeutic target for the treatment of diet-induced hepatic steatosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Cell Line
  • Diet, High-Fat*
  • Disease Susceptibility
  • Fatty Liver / etiology*
  • Fatty Liver / metabolism*
  • Fatty Liver / pathology
  • Gene Expression
  • Gene Expression Profiling
  • Gene Knockdown Techniques
  • Gene Targeting
  • Hedgehog Proteins / metabolism
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Humans
  • Immunohistochemistry
  • Mice
  • Mice, Knockout
  • Obesity / complications
  • Obesity / etiology
  • Obesity / metabolism
  • PPAR gamma / metabolism
  • Protein Binding
  • RNA, Long Noncoding / genetics*
  • RNA-Binding Proteins
  • Signal Transduction

Substances

  • Biomarkers
  • Hedgehog Proteins
  • IGF2BP2 protein, mouse
  • PPAR gamma
  • RNA, Long Noncoding
  • RNA-Binding Proteins