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Am J Physiol Lung Cell Mol Physiol 295: L38-L43, 2008. First published April 25, 2008; doi:10.1152/ajplung.00280.2007
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Pulmonary alveolar epithelial uptake of S-nitrosothiols is regulated by L-type amino acid transporter

Olivia M. Granillo,4,* Mulugu V. Brahmajothi,1,* Sheng Li,2 A. Richard Whorton,2 S. Nicholas Mason,1 Timothy J. McMahon,3 and Richard L. Auten1

1Division of Neonatal Medicine, Neonatal-Perinatal Research Institute, Department of Pediatrics, 2Department of Pharmacology and Cancer Biology, 3Division of Pulmonary and Critical Care Medicine, Department of Medicine, and 4School of Medicine, Duke University Medical Center, Durham, North Carolina

Submitted 19 July 2007 ; accepted in final form 15 April 2008

Nitric oxide (NO) effects are often mediated via S-nitrosothiol (SNO) formation; SNO uptake has recently been shown to be mediated in some cell types via system L-type amino acid transporters (LAT-1, 2). Inhaled NO therapy may exert some biological effects via SNO formation. We therefore sought to determine if pulmonary epithelial SNO uptake depended on LAT or peptide transporter 2 (PEPT2). Both LAT-1 and PEPT2 proteins were detected by immunoblot and immunocytochemistry in L2 cells and rat lung. We tested SNO uptake through the transporters by exposing rat alveolar epithelial cells (L2 and type II) to RSNOs: S-nitrosoglutathione, S-nitrosocysteinylglycine (SNO-Cys-Gly), S-nitrosocysteine (CSNO), and to NO donor diethylamine NONOate (DEA-NONOate). SNO was detected in cell lysates by ozone chemiluminescence. NO uptake was detected by fluorescence in alveolar epithelial cells loaded with 4-amino-5-methylamino-2',7'-difluorofluorescein (DAF-FM) diacetate cultured in submersion and exposed to RSNOs and DEA NONOate. Addition of L-Cys but not D-Cys to RSNOs or DEA NONOate increased SNO and DAF-FM signal that was inhibited by coincubation with LAT competitors. Incubation of cells with PEPT2 substrate SNO-Cys-Gly showed no increase in SNO or DAF-FM signal unless incubated with L-Cys. This was unaffected by PEPT2 inhibition. We conclude that RSNOs (thionitrites, S-nitrosothiols) and NO enter alveolar epithelial cells predominantly by S-nitrosation of L-Cys, which is then imported through LAT.

peptide transporter 2; type II alveolar epithelium; S-nitrosylation; nitric oxide



Address for reprint requests and other correspondence: R. L. Auten, DUMC Box 3373, Duke Univ., Durham, NC 27710 (e-mail: auten{at}duke.edu)







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