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Oxido-reductive regulation of vascular remodeling by receptor tyrosine kinase ROS1
Ziad A. Ali, … , Thomas Quertermous, Euan A. Ashley
Ziad A. Ali, … , Thomas Quertermous, Euan A. Ashley
Published November 17, 2014
Citation Information: J Clin Invest. 2014;124(12):5159-5174. https://doi.org/10.1172/JCI77484.
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Research Article

Oxido-reductive regulation of vascular remodeling by receptor tyrosine kinase ROS1

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Abstract

Angioplasty and stenting is the primary treatment for flow-limiting atherosclerosis; however, this strategy is limited by pathological vascular remodeling. Using a systems approach, we identified a role for the network hub gene glutathione peroxidase-1 (GPX1) in pathological remodeling following human blood vessel stenting. Constitutive deletion of Gpx1 in atherosclerotic mice recapitulated this phenotype of increased vascular smooth muscle cell (VSMC) proliferation and plaque formation. In an independent patient cohort, gene variant pair analysis identified an interaction of GPX1 with the orphan protooncogene receptor tyrosine kinase ROS1. A meta-analysis of the only genome-wide association studies of human neointima-induced in-stent stenosis confirmed the association of the ROS1 variant with pathological remodeling. Decreased GPX1 expression in atherosclerotic mice led to reductive stress via a time-dependent increase in glutathione, corresponding to phosphorylation of the ROS1 kinase activation site Y2274. Loss of GPX1 function was associated with both oxidative and reductive stress, the latter driving ROS1 activity via s-glutathiolation of critical residues of the ROS1 tyrosine phosphatase SHP-2. ROS1 inhibition with crizotinib and deglutathiolation of SHP-2 abolished GPX1-mediated increases in VSMC proliferation while leaving endothelialization intact. Our results indicate that GPX1-dependent alterations in oxido-reductive stress promote ROS1 activation and mediate vascular remodeling.

Authors

Ziad A. Ali, Vinicio de Jesus Perez, Ke Yuan, Mark Orcholski, Stephen Pan, Wei Qi, Gaurav Chopra, Christopher Adams, Yoko Kojima, Nicholas J. Leeper, Xiumei Qu, Kathia Zaleta-Rivera, Kimihiko Kato, Yoshiji Yamada, Mitsutoshi Oguri, Allan Kuchinsky, Stanley L. Hazen, J. Wouter Jukema, Santhi K. Ganesh, Elizabeth G. Nabel, Keith Channon, Martin B. Leon, Alain Charest, Thomas Quertermous, Euan A. Ashley

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Figure 2

Stent endothelialization is impaired in Gpx1-deficient mice.

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Stent endothelialization is impaired in Gpx1-deficient mice.
In Gpx1–/– ...
In Gpx1–/– Apoe–/– and Gpx1+/+ Apoe–/– mice additionally expressing β-gal (LacZ) targeted to endothelial cells (Tie2), en face macroscopic vessel images identify (A) stents struts (black arrowheads), endothelium (blue stain) on the luminal surface, and (B) areas with no endothelium (gray arrowheads). Scale bar: 0.5 mm. (C) Reendothelialization was impaired in Gpx1–/– Apoe–/– Tie2-LacZ+ mice 4 weeks following BAS. Left panel shows high-power en face microscopy images of the luminal surface of the stented vessel. Right panel shows cross-sectional histomorphometry. *P < 0.05. n = 6–10 mice/group. White arrowheads denote stent struts; black arrowheads denote endothelial cells. Scale bar: 50 μm.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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