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Down-regulation effects of IFN-α on p11, 5-htr1b and 5-HTR4 protein levels were affected by NH4CL or MG132 treatment in SH-sy5y cells

  • Jiqiang Guo
  • , Huaxia Ding
  • , Zhuangwei Lv
  • , Junna Jiao
  • , Hui Wang
  • , Yanhong Ji

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

In previous studies, we found interferon-α (IFN-α) could reduce protein levels of p11, 5-hydroxytryptamine receptor 1b (5-HT1b) and 5-hydroxytryptamine receptor 4 (5-HT4), but does not influence their messenger RNA levels in SH-sy5y cells. Thus, we investigated the post-transcriptional modulation of these molecules by IFN-α. SH-sy5y cells were treated with IFN-α, NH4Cl or MG132 alone or in combination, and then the protein levels of p11, 5-HT1b and 5-HT4 were analyzed by western blots. The regulatory effects of p11 on 5-HT1b and 5-HT4 were also determined in p11 knock-down cells. NH4Cl but not MG132 could reverse the protein level of p11 in IFN-α-treated SH-sy5y cells. MG132 could recover the protein levels of 5-HT1b and 5-HT4 in p11 knock-down cells. The down-regulation effects of IFN-α on p11, 5-HT1b and 5-HT4 were associated with the lysosome and ubiquitin–proteasome-mediated pathways. p11 was identified as a potent regulator to modulate the ubiquitination of 5-HT1b and 5-HT4. Therefore, it could be potential target therapies in IFN-α-induced depression.

Original languageEnglish
Article number101
JournalJournal of biosciences
Volume44
Issue number4
DOIs
StatePublished - 1 Sep 2019

Keywords

  • 5-Hydroxytryptamine receptor 4
  • 5-hydroxytryptamine receptor 1b
  • MG132
  • NHCl
  • interferon-α
  • p11

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