Different anti-oxidant effects of thioredoxin 1 and thioredoxin 2 in retinal epithelial cells

Eriko Sugano, Hitomi Isago, Namie Murayama, Makoto Tamai, Hiroshi Tomita

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

Age-related macular degeneration (AMD) affects the retina and is the most common cause of blindness in elderly persons in developed countries. The retina is constantly subjected to oxidative stress; to avoid the effects of oxidative stress, retinal pigment epithelial (RPE) cells possess potent anti-oxidant systems. Disruption of these systems leads to dysfunction of RPE cells, which then accelerates the development of AMD. Here, we investigated the role of thioredoxins (TRXs), scavengers of intracellular reactive oxygen species, by assessing the effect of TRX overexpression on cell viability, morphology, NF-κB expression, and mitochondrial membrane potential, in RPE cells. TRX-overexpressing cell lines were generated by infection of an established human RPE cell line (ARPE) with adeno-associated virus vectors encoding either TRX1 or TRX2. We showed that overexpression of TRXs reduced cell death caused by 4-hydroxynonenal (4-HNE)-induced oxidative stress; TRX2 was more effective than TRX1 in promoting cell survival. 4-HNE caused perinuclear NF-κB accumulation, which was absent in TRX-overexpressing cells. Moreover, overexpression of TRXs prevented depolarization of mitochondrial membranes; again, TRX2 was more effective than TRX1 in maintaining the membrane potential. The difference in the protective effects of these TRXs against oxidative stress may be due to their expression profile. TRX2 was expressed in the mitochondria, while TRX1 was expressed in the cytoplasm. Thus, TRX2 may directly protect mitochondria by preventing depolarization. These results demonstrate that TRXs are potent antioxidant proteins in RPE cells and their direct effect on mitochondria may be a key to prevent oxidative stress.

Original languageEnglish
Pages (from-to)81-88
Number of pages8
JournalCell structure and function
Volume38
Issue number1
DOIs
Publication statusPublished - 2013

Keywords

  • Adeno-associated virus
  • Age-related macular degeneration
  • Oxidative stress
  • Retinal epithelial cells
  • Thioredoxin

ASJC Scopus subject areas

  • Physiology
  • Molecular Biology
  • Cell Biology

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