Hepcidin inhibits autophagy in intracerebral hemorrhage models in vitro and in vivo

Mol Cell Neurosci. 2021 Mar:111:103589. doi: 10.1016/j.mcn.2021.103589. Epub 2021 Jan 8.

Abstract

Iron has a key role in the activation of the autophagic pathway in rats with intracerebral hemorrhage (ICH), and hepcidin has the ability to reduce brain iron in ICH-rats. We therefore hypothesized that hepcidin might be able to inhibit autophagy by reducing iron in an ICH brain. Here, we investigated the effects of Ad-hepcidin and/or hepcidin peptide on autophagic activities in ICH models in vitro and in vivo. We demonstrated that ad-hepcidin and hepcidin peptide both inhibited hemin-induced increase in LC3-II/LC3-I conversion ratio and reversed the reduction in p62 content in cortical neurons in vitro. We also showed that ad-hepcidin inhibited ICH-induced increase in LC3-II/LC3-I conversion ratio and reversed ICH-induced reduction in p62 content in the brain cortex of rats in vivo. Based on these findings plus previous data on the effects of ad-hepcidin and/or hepcidin peptide on iron contents in ICH models, we suggested that hepcidin-induced inhibition of autophagy might be mediated via reducing iron in hemin-treated neurons in vitro and ICH-rat brain in vivo.

Keywords: Autophagy; Hemin; Hepcidin; In vitro and in vivo study; Intracerebral hemorrhage (ICH); LC3-II/LC3-I conversion ratio; p62 (SQSTM1).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Autophagy*
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • Cerebral Cortex / metabolism
  • Cerebral Hemorrhage / metabolism*
  • Genetic Vectors / genetics
  • Hepcidins / genetics
  • Hepcidins / metabolism*
  • Male
  • Microtubule-Associated Proteins / metabolism
  • Neurons / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Sequestosome-1 Protein / metabolism

Substances

  • Hepcidins
  • LC3 protein, rat
  • Microtubule-Associated Proteins
  • Recombinant Proteins
  • Sequestosome-1 Protein
  • Sqstm1 protein, rat