Oxidative stress impairs the stimulatory effect of S100 proteins on protein phosphatase 5 activity

Fuminori Yamaguchi, Mitsumasa Tsuchiya, Seiko Shimamoto, Tomohito Fujimoto, Hiroshi Tokumitsu, Masaaki Tokuda, Ryoji Kobayashi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Oxidative stress is the consequence of an imbalance between the production of harmful reactive oxygen species and the cellular antioxidant system for neutralization, and it activates multiple intracellular signaling pathways, including apoptosis signal-regulating kinase 1 (ASK1). Protein phosphatase 5 (PP5) is a serine/ threonine phosphatase involved in oxidative stress responses. Previously, we reported that S100 proteins activate PP5 in a calcium-dependent manner. S100 proteins belong to a family of small EF-hand calciumbinding proteins involved in many processes such as cell proliferation, differentiation, apoptosis, and inflammation. Therefore, we investigated the effects of oxidative stress on S100 proteins, their interaction with PP5, and PP5 enzyme activity. Recombinant S100A2 was easily air-oxidized or Cu-oxidized, and oxidized S100A2 formed cross-linked dimers and higher molecular-mass complexes. The binding of oxidized S100A2 to PP5 was reduced, resulting in decreased PP5 activation in vitro. Oxidation also impaired S100A1, S100A6, S100B, and S100P to activate PP5, although the low dose of oxidized S100 proteins still activated PP5. Hydrogen peroxide (H2O2) induced S100A2 oxidation in human keratinocytes (HaCaT) and human hepatocellular carcinoma (Huh-7) cells. Furthermore, H2O2 reduced the binding of S100A2 to PP5 and decreased PP5 activation in HaCaT and Huh-7 cells. Importantly, even the low dose of S100A2 achieved by knocking down increased dephosphorylation of ASK1 and reduced caspase 3/7 activity in Huh-7 cells treated with H2O2. These results indicate that oxidative stress impairs the ability of S100 proteins to bind and activate PP5, which in turn modulates the ASK1-mediated signaling cascades involved in apoptosis.

Original languageEnglish
Pages (from-to)67-78
Number of pages12
JournalTohoku Journal of Experimental Medicine
Volume240
Issue number1
DOIs
Publication statusPublished - Sep 1 2016
Externally publishedYes

Fingerprint

Oxidative stress
S100 Proteins
Oxidative Stress
MAP Kinase Kinase Kinase 5
protein phosphatase 5
Chemical activation
Apoptosis
EF Hand Motifs
Caspase 7
Oxidation
Phosphoprotein Phosphatases
Cell proliferation
Enzyme activity
Molecular mass
Keratinocytes
Caspase 3
Dimers
Hydrogen Peroxide
Cell Differentiation
Hepatocellular Carcinoma

Keywords

  • HaCaT
  • Huh-7
  • Oxidative stress
  • Protein phosphatase 5
  • S100 protein

ASJC Scopus subject areas

  • Medicine(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Oxidative stress impairs the stimulatory effect of S100 proteins on protein phosphatase 5 activity. / Yamaguchi, Fuminori; Tsuchiya, Mitsumasa; Shimamoto, Seiko; Fujimoto, Tomohito; Tokumitsu, Hiroshi; Tokuda, Masaaki; Kobayashi, Ryoji.

In: Tohoku Journal of Experimental Medicine, Vol. 240, No. 1, 01.09.2016, p. 67-78.

Research output: Contribution to journalArticle

Yamaguchi, Fuminori ; Tsuchiya, Mitsumasa ; Shimamoto, Seiko ; Fujimoto, Tomohito ; Tokumitsu, Hiroshi ; Tokuda, Masaaki ; Kobayashi, Ryoji. / Oxidative stress impairs the stimulatory effect of S100 proteins on protein phosphatase 5 activity. In: Tohoku Journal of Experimental Medicine. 2016 ; Vol. 240, No. 1. pp. 67-78.
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