NYMC Faculty Publications

Sepiapterin Reductase Mediates Chemical Redox Cycling in Lung Epithelial Cells

Author Type(s)

Faculty

DOI

10.1074/jbc.M112.402164

Journal Title

The Journal of Biological Chemistry

First Page

19221

Last Page

19237

Document Type

Article

Publication Date

6-28-2013

Department

Medicine

Keywords

Alcohol Oxidoreductases, Animals, Biopterins, Cell Line, Tumor, Dose-Response Relationship, Drug, Enzyme Inhibitors, Epithelial Cells, Genetic Vectors, Humans, Lung, Mice, Models, Chemical, Models, Molecular, Mutagenesis, Site-Directed, Oxidation-Reduction, Oxidative Stress, Quinones, Reactive Oxygen Species, Recombinant Proteins

Disciplines

Medicine and Health Sciences

Abstract

In the lung, chemical redox cycling generates highly toxic reactive oxygen species that can cause alveolar inflammation and damage to the epithelium, as well as fibrosis. In this study, we identified a cytosolic NADPH-dependent redox cycling activity in mouse lung epithelial cells as sepiapterin reductase (SPR), an enzyme important for the biosynthesis of tetrahydrobiopterin. Human SPR was cloned and characterized. In addition to reducing sepiapterin, SPR mediated chemical redox cycling of bipyridinium herbicides and various quinones; this activity was greatest for 1,2-naphthoquinone followed by 9,10-phenanthrenequinone, 1,4-naphthoquinone, menadione, and 2,3-dimethyl-1,4-naphthoquinone. Whereas redox cycling chemicals inhibited sepiapterin reduction, sepiapterin had no effect on redox cycling. Additionally, inhibitors such as dicoumarol, N-acetylserotonin, and indomethacin blocked sepiapterin reduction, with no effect on redox cycling. Non-redox cycling quinones, including benzoquinone and phenylquinone, were competitive inhibitors of sepiapterin reduction but noncompetitive redox cycling inhibitors. Site-directed mutagenesis of the SPR C-terminal substrate-binding site (D257H) completely inhibited sepiapterin reduction but had minimal effects on redox cycling. These data indicate that SPR-mediated reduction of sepiapterin and redox cycling occur by distinct mechanisms. The identification of SPR as a key enzyme mediating chemical redox cycling suggests that it may be important in generating cytotoxic reactive oxygen species in the lung. This activity, together with inhibition of sepiapterin reduction by redox-active chemicals and consequent deficiencies in tetrahydrobiopterin, may contribute to tissue injury.

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