Oxidation of PKGIα mediates an endogenous adaptation to pulmonary hypertension

Proc Natl Acad Sci U S A. 2019 Jun 25;116(26):13016-13025. doi: 10.1073/pnas.1904064116. Epub 2019 Jun 11.

Abstract

Chronic hypoxia causes pulmonary hypertension (PH), vascular remodeling, right ventricular (RV) hypertrophy, and cardiac failure. Protein kinase G Iα (PKGIα) is susceptible to oxidation, forming an interprotein disulfide homodimer associated with kinase targeting involved in vasodilation. Here we report increased disulfide PKGIα in pulmonary arteries from mice with hypoxic PH or lungs from patients with pulmonary arterial hypertension. This oxidation is likely caused by oxidants derived from NADPH oxidase-4, superoxide dismutase 3, and cystathionine γ-lyase, enzymes that were concomitantly increased in these samples. Indeed, products that may arise from these enzymes, including hydrogen peroxide, glutathione disulfide, and protein-bound persulfides, were increased in the plasma of hypoxic mice. Furthermore, low-molecular-weight hydropersulfides, which can serve as "superreductants" were attenuated in hypoxic tissues, consistent with systemic oxidative stress and the oxidation of PKGIα observed. Inhibiting cystathionine γ-lyase resulted in decreased hypoxia-induced disulfide PKGIα and more severe PH phenotype in wild-type mice, but not in Cys42Ser PKGIα knock-in (KI) mice that are resistant to oxidation. In addition, KI mice also developed potentiated PH during hypoxia alone. Thus, oxidation of PKGIα is an adaptive mechanism that limits PH, a concept further supported by polysulfide treatment abrogating hypoxia-induced RV hypertrophy in wild-type, but not in the KI, mice. Unbiased transcriptomic analysis of hypoxic lungs before structural remodeling identified up-regulation of endothelial-to-mesenchymal transition pathways in the KI compared with wild-type mice. Thus, disulfide PKGIα is an intrinsic adaptive mechanism that attenuates PH progression not only by promoting vasodilation but also by limiting maladaptive growth and fibrosis signaling.

Keywords: hypoxia; oxidative stress; protein kinase G; pulmonary hypertension; redox.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Cell Line
  • Cyclic GMP-Dependent Protein Kinase Type I / chemistry
  • Cyclic GMP-Dependent Protein Kinase Type I / metabolism*
  • Cystathionine gamma-Lyase / antagonists & inhibitors
  • Cystathionine gamma-Lyase / metabolism
  • Disease Models, Animal
  • Disease Progression
  • Disulfides / chemistry
  • Female
  • Fibrosis
  • Gene Knock-In Techniques
  • Humans
  • Hypertension, Pulmonary / blood
  • Hypertension, Pulmonary / etiology
  • Hypertension, Pulmonary / pathology*
  • Hypertension, Pulmonary / prevention & control
  • Hypoxia / blood
  • Hypoxia / complications*
  • Hypoxia / drug therapy
  • Lung / blood supply
  • Lung / pathology
  • Male
  • Mice
  • Mice, Transgenic
  • Middle Aged
  • Oxidants / metabolism
  • Oxidation-Reduction / drug effects
  • Oxidative Stress / drug effects
  • Pulmonary Artery / pathology*
  • Sulfides / administration & dosage
  • Sulfides / blood
  • Sulfides / metabolism
  • Up-Regulation
  • Vasoconstriction / drug effects
  • Vasodilation / drug effects

Substances

  • Disulfides
  • Oxidants
  • Sulfides
  • persulfides
  • polysulfide
  • Cyclic GMP-Dependent Protein Kinase Type I
  • PRKG1 protein, human
  • Prkg1 protein, mouse
  • Cystathionine gamma-Lyase
  • sodium bisulfide