Impaired endothelial nitric oxide synthase homodimer formation triggers development of transplant vasculopathy - Insights from a murine aortic transplantation model

Rupert Oberhuber, Gregor Riede, Benno Cardini, David Bernhard, Barbara Messner, Katrin Watschinger, Christina Steger, Gerald Brandacher, Johann Pratschke, Georg Golderer, Ernst R. Werner, Manuel Maglione

Research output: Contribution to journalArticle

Abstract

Transplant vasculopathy (TV) represents a major obstacle to long-term graft survival and correlates with severity of ischemia reperfusion injury (IRI). Donor administration of the nitric oxide synthases (NOS) co-factor tetrahydrobiopterin has been shown to prevent IRI. Herein, we analysed whether tetrahydrobiopterin is also involved in TV development. Using a fully allogeneic mismatched (BALB/c to C57BL/6) murine aortic transplantation model grafts subjected to long cold ischemia time developed severe TV with intimal hyperplasia (α-smooth muscle actin positive cells in the neointima) and endothelial activation (increased P-selectin expression). Donor pretreatment with tetrahydrobiopterin significantly minimised these changes resulting in only marginal TV development. Severe TV observed in the non-treated group was associated with increased protein oxidation and increased occurrence of endothelial NOS monomers in the aortic grafts already during graft procurement. Tetrahydrobiopterin supplementation of the donor prevented all these early oxidative changes in the graft. Non-treated allogeneic grafts without cold ischemia time and syngeneic grafts did not develop any TV. We identified early protein oxidation and impaired endothelial NOS homodimer formation as plausible mechanistic explanation for the crucial role of IRI in triggering TV in transplanted aortic grafts. Therefore, targeting endothelial NOS in the donor represents a promising strategy to minimise TV.

Original languageEnglish (US)
Article number37917
JournalScientific Reports
Volume6
DOIs
StatePublished - Nov 24 2016

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Nitric Oxide Synthase Type III
Transplantation
Transplants
Reperfusion Injury
Cold Ischemia
Tunica Intima
Neointima
P-Selectin
Graft Survival
Nitric Oxide Synthase
Hyperplasia
Smooth Muscle
Actins

ASJC Scopus subject areas

  • General

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Impaired endothelial nitric oxide synthase homodimer formation triggers development of transplant vasculopathy - Insights from a murine aortic transplantation model. / Oberhuber, Rupert; Riede, Gregor; Cardini, Benno; Bernhard, David; Messner, Barbara; Watschinger, Katrin; Steger, Christina; Brandacher, Gerald; Pratschke, Johann; Golderer, Georg; Werner, Ernst R.; Maglione, Manuel.

In: Scientific Reports, Vol. 6, 37917, 24.11.2016.

Research output: Contribution to journalArticle

Oberhuber, R, Riede, G, Cardini, B, Bernhard, D, Messner, B, Watschinger, K, Steger, C, Brandacher, G, Pratschke, J, Golderer, G, Werner, ER & Maglione, M 2016, 'Impaired endothelial nitric oxide synthase homodimer formation triggers development of transplant vasculopathy - Insights from a murine aortic transplantation model', Scientific Reports, vol. 6, 37917. https://doi.org/10.1038/srep37917
Oberhuber, Rupert ; Riede, Gregor ; Cardini, Benno ; Bernhard, David ; Messner, Barbara ; Watschinger, Katrin ; Steger, Christina ; Brandacher, Gerald ; Pratschke, Johann ; Golderer, Georg ; Werner, Ernst R. ; Maglione, Manuel. / Impaired endothelial nitric oxide synthase homodimer formation triggers development of transplant vasculopathy - Insights from a murine aortic transplantation model. In: Scientific Reports. 2016 ; Vol. 6.
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