HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

miR221 regulates TGF-β1-induced HSC activation through inhibiting autophagy by directly targeting LAMP2.

Abstract
Liver fibrosis is a serious threat to human life and health. Activated hepatic stellate cells (HSCs) play a key role in the occurrence and development of liver fibrosis. Studies have reported that microRNAs (miRNAs/miRs) are involved in the pathological process of fibrosis, as well as its relevance in clinical diagnosis. However, the role of miR221 in hepatic fibrosis remains controversial. Remarkably, transforming growth factor‑β (TGF‑β1) caused HSC dysfunction in autophagic activation, characterized by an increase in P62 aggregation and LC3II expression. The present study aimed to determine whether autophagy regulates hepatic fibrosis by mediating HSC activation and explore the potential targets leading to the sequence of events associated with miR221. The expression of miR221 was quantified in a liver fibrosis model in vivo and in vitro, and its specific target gene lysosome‑associated membrane glycoprotein 2 (LAMP2) was predicted by bioinformatics. The results showed that the expression levels of collagen‑I (COL‑I) and α‑smooth muscle actin (α‑SMA) were increased in miR221‑overexpressing LX2 cells, while the autophagy inducer rapamycin reversed the inhibition of autophagic flux induced by miR221. Additionally, the overexpression of LAMP2 could significantly inhibit TGF‑β1‑induced COL‑I and α‑SMA expression, which was similar to the effect of the miR221 inhibitor on the regulation of TGF‑β1‑induced HSC activation. These results indicated that miR221 may regulate TGF‑β1‑induced HSC activation through inhibiting autolysosome function by directly targeting LAMP2. The molecular mechanism of miR221 in regulating TGF‑β1‑induced HSC activation may provide novel insight into therapies to ameliorate the pathological progression of liver fibrosis.
AuthorsRan Cheng, Hao Xu, Yang Hong
JournalMolecular medicine reports (Mol Med Rep) Vol. 24 Issue 5 (Nov 2021) ISSN: 1791-3004 [Electronic] Greece
PMID34498712 (Publication Type: Journal Article)
Chemical References
  • Biomarkers
  • Lysosomal-Associated Membrane Protein 2
  • MIRN221 microRNA, mouse
  • MicroRNAs
  • Tgfb1 protein, mouse
  • Transforming Growth Factor beta1
Topics
  • Animals
  • Apoptosis (physiology)
  • Autophagy (physiology)
  • Biomarkers (metabolism)
  • Cell Proliferation (physiology)
  • Cells, Cultured
  • Hepatic Stellate Cells (metabolism, pathology)
  • Liver Cirrhosis (genetics, metabolism, pathology)
  • Lysosomal-Associated Membrane Protein 2 (genetics, metabolism)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs (genetics)
  • Transforming Growth Factor beta1 (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: