Oxidation of extracellular cysteine/cystine redox state in bleomycin-induced lung fibrosis

Smita Iyer, Allan M. Ramirez, Jeffrey D. Ritzenthaler, Edilson Torres-Gonzalez, Susanne Roser-Page, Ana L. Mora, Kenneth L. Brigham, Dean P. Jones, Jesse Roman, Mauricio Rojas

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

Several lines of evidence indicate that depletion of glutathione (GSH), a critical thiol antioxidant, is associated with the pathogenesis of idiopathic pulmonary fibrosis (IPF). However, GSH synthesis depends on the amino acid cysteine (Cys), and relatively little is known about the regulation of Cys in fibrosis. Cys and its disulfide, cystine (CySS), constitute the most abundant low-molecular weight thiol/disulfide redox couple in the plasma, and the Cys/CySS redox state (Eh Cys/CySS) is oxidized in association with age and smoking, known risk factors for IPF. Furthermore, oxidized Eh Cys/CySS in the culture media of lung fibroblasts stimulates proliferation and expression of transitional matrix components. The present study was undertaken to determine whether bleomycin-induced lung fibrosis is associated with a decrease in Cys and/or an oxidation of the Cys/CySS redox state and to determine whether these changes were associated with changes in Eh GSH/glutathione disulfide (GSSG). We observed distinct effects on plasma GSH and Cys redox systems during the progression of bleomycin-induced lung injury. Plasma Eh GSH/GSSG was selectively oxidized during the proinflammatory phase, whereas oxidation of Eh Cys/CySS occurred at the fibrotic phase. In the epithelial lining fluid, oxidation of Eh Cys/CySS was due to decreased food intake. Thus the data show that decreased precursor availability and enhanced oxidation of Cys each contribute to the oxidation of extracellular Cys/CySS redox state in bleomycin-induced lung fibrosis.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Volume296
Issue number1
DOIs
StatePublished - Jan 1 2009
Externally publishedYes

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Cystine
Oxidation-Reduction
Cysteine
Fibrosis
Lung
Glutathione Disulfide
Idiopathic Pulmonary Fibrosis
Bleomycin
Sulfhydryl Compounds
Disulfides
indium-bleomycin
Lung Injury
Glutathione
Culture Media
Fibroblasts

Keywords

  • Diet
  • Glutathione
  • Idiopathic pulmonary fibrosis
  • Oxidative stress

ASJC Scopus subject areas

  • Physiology
  • Pulmonary and Respiratory Medicine
  • Cell Biology
  • Physiology (medical)

Cite this

Oxidation of extracellular cysteine/cystine redox state in bleomycin-induced lung fibrosis. / Iyer, Smita; Ramirez, Allan M.; Ritzenthaler, Jeffrey D.; Torres-Gonzalez, Edilson; Roser-Page, Susanne; Mora, Ana L.; Brigham, Kenneth L.; Jones, Dean P.; Roman, Jesse; Rojas, Mauricio.

In: American Journal of Physiology - Lung Cellular and Molecular Physiology, Vol. 296, No. 1, 01.01.2009.

Research output: Contribution to journalArticle

Iyer, S, Ramirez, AM, Ritzenthaler, JD, Torres-Gonzalez, E, Roser-Page, S, Mora, AL, Brigham, KL, Jones, DP, Roman, J & Rojas, M 2009, 'Oxidation of extracellular cysteine/cystine redox state in bleomycin-induced lung fibrosis', American Journal of Physiology - Lung Cellular and Molecular Physiology, vol. 296, no. 1. https://doi.org/10.1152/ajplung.90401.2008
Iyer, Smita ; Ramirez, Allan M. ; Ritzenthaler, Jeffrey D. ; Torres-Gonzalez, Edilson ; Roser-Page, Susanne ; Mora, Ana L. ; Brigham, Kenneth L. ; Jones, Dean P. ; Roman, Jesse ; Rojas, Mauricio. / Oxidation of extracellular cysteine/cystine redox state in bleomycin-induced lung fibrosis. In: American Journal of Physiology - Lung Cellular and Molecular Physiology. 2009 ; Vol. 296, No. 1.
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