Crocin inhibits the activation of mouse hepatic stellate cells via the lnc-LFAR1/MTF-1/GDNF pathway

Cell Cycle. 2020 Dec;19(24):3480-3490. doi: 10.1080/15384101.2020.1848064. Epub 2020 Dec 9.

Abstract

Crocin is the main monomer of saffron, which is a momentous component of traditional Chinese medicine Lang Qing A Ta. Here, we tried to probe into the role of crocin in liver fibrosis. Hematoxylin-eosin staining and Sirius Red staining were used to observe the pathological changes of liver tissues. After hepatic stellate cells (HSCs) were isolated from liver tissues, lnc-LFAR1, MTF-1, GDNF, and α-SMA expressions were detected by qRT-PCR and western blot. Immunohistochemistry and immunofluorescence were used to detect α-SMA expression. Chromatin immunoprecipitation was used to analyze the binding of MTF-1 to the GDNF promoter. Moreover, the dual-luciferase reporter gene, RNA pull-down, and RNA immunoprecipitation were used to clarify the interaction between MTF-1 and GDNF, lnc-LFAR1 and MTF-1. The degree of liver fibrosis was more severe in the mice from the liver fibrosis model, while the liver fibrosis was alleviated by the injection of crocin. lnc-LFAR1, GDNF, and α-SMA were up-regulated, and MTF-1 was down-regulated in liver fibrosis tissues and cells, while these trends were reversed after the injection of crocin. Besides, lnc-LFAR1 negatively regulated MTF-1 expression, and positively regulated GDNF and α-SMA expressions, and MTF-1 was enriched in the promoter region of GDNF. Furthermore, the cellular direct interactions between MTF-1 and GDNF, lnc-LFAR1 and MTF-1 were verified. In vivo experiments confirmed the relief of crocin on liver fibrosis. Our research expounded that crocin restrained the activation of HSCs through the lnc-LFAR1/MTF-1/GDNF axis, thereby ameliorating liver fibrosis.

Keywords: Crocin; GDNF; MTF-1; hepatic stellate cells; lnc-LFAR1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carotenoids / administration & dosage*
  • Cells, Cultured
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Disease Models, Animal
  • Down-Regulation / drug effects
  • Down-Regulation / genetics
  • Drugs, Chinese Herbal / administration & dosage*
  • Glial Cell Line-Derived Neurotrophic Factor / metabolism*
  • Hepatic Stellate Cells / metabolism*
  • Liver Cirrhosis / metabolism*
  • Liver Cirrhosis / pathology
  • Liver Cirrhosis / therapy*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Phytotherapy / methods*
  • Promoter Regions, Genetic
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / metabolism*
  • Signal Transduction / drug effects*
  • Signal Transduction / genetics
  • Transcription Factor MTF-1
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transfection
  • Treatment Outcome
  • Up-Regulation / drug effects
  • Up-Regulation / genetics

Substances

  • DNA-Binding Proteins
  • Drugs, Chinese Herbal
  • Gdnf protein, mouse
  • Glial Cell Line-Derived Neurotrophic Factor
  • RNA, Long Noncoding
  • Transcription Factors
  • Carotenoids
  • crocin

Grants and funding

This work was supported by the National Natural Science Foundation of China [No. 81704196], Jiangsu Province 333 High-level Talent Training Project [BRA2018408], Medical Research Project of Jiangsu Commission of Health [H2019073].