Hydrogen gas protects IP3Rs by reducing disulfide bridges in human keratinocytes under oxidative stress

Ching Ying Wu, Wen Li Hsu, Ming Hsien Tsai, Jui Lin Liang, Jian He Lu, Chia Jung Yen, Hsin Su Yu, Mami Noda, Chi Yu Lu, Chu Huang Chen, Shian Jang Yan, Tohru Yoshioka

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

Based on the oxidative stress theory, aging derives from the accumulation of oxidized proteins induced by reactive oxygen species (ROS) in the cytoplasm. Hydrogen peroxide (H2O2) elicits ROS that induces skin aging through oxidation of proteins, forming disulfide bridges with cysteine or methionine sulfhydryl groups. Decreased Ca2+ signaling is observed in aged cells, probably secondary to the formation of disulfide bonds among Ca2+ signaling-related proteins. Skin aging processes are modeled by treating keratinocytes with H2O2. In the present study, H2O2 dose-dependently impaired the adenosine triphosphate (ATP)-induced Ca2+ response, which was partially protected via co-treatment with β-mercaptoethanol, resulting in reduced disulfide bond formation in inositol 1, 4, 5-trisphosphate receptors (IP3Rs). Molecular hydrogen (H2) was found to be more effectively protected H2O2-induced IP3R1 dysfunction by reducing disulfide bonds, rather than quenching ROS. In conclusion, skin aging processes may involve ROS-induced protein dysfunction due to disulfide bond formation, H2 can protect oxidation of this process.

Original languageEnglish
Article number3606
JournalScientific reports
Volume7
Issue number1
DOIs
Publication statusPublished - 2017 Dec 1

All Science Journal Classification (ASJC) codes

  • General

Fingerprint Dive into the research topics of 'Hydrogen gas protects IP3Rs by reducing disulfide bridges in human keratinocytes under oxidative stress'. Together they form a unique fingerprint.

Cite this