[HTML][HTML] NOX5 expression is increased in intramyocardial blood vessels and cardiomyocytes after acute myocardial infarction in humans

NE Hahn, C Meischl, T Kawahara, RJP Musters… - The American journal of …, 2012 - Elsevier
NE Hahn, C Meischl, T Kawahara, RJP Musters, VMJ Verhoef, J van der Velden, ABA Vonk…
The American journal of pathology, 2012Elsevier
Reactive oxygen species producing NADPH oxidases play important roles under different
(patho) physiological conditions. NOX1, NOX2, and NOX4 are important sources of reactive
oxygen species in the heart, but knowledge of the calcium-dependent NOX5 in the heart is
lacking. The presence of NOX5 was studied via RT-PCR in heart tissue from patients with
end-stage heart failure; the tissue was obtained during cardiac transplantation surgery.
NOX5 positivity and cellular localization were studied via IHC and digital-imaging …
Reactive oxygen species producing NADPH oxidases play important roles under different (patho)physiological conditions. NOX1, NOX2, and NOX4 are important sources of reactive oxygen species in the heart, but knowledge of the calcium-dependent NOX5 in the heart is lacking. The presence of NOX5 was studied via RT-PCR in heart tissue from patients with end-stage heart failure; the tissue was obtained during cardiac transplantation surgery. NOX5 positivity and cellular localization were studied via IHC and digital-imaging microscopy in heart tissues of patients who did not have heart disease and in infarction areas of patients who died of myocardial infarctions of different durations. Furthermore, NOX5 expression was analyzed in vitro by using Western blot analysis. NOX5 RNA was found in the hearts of controls and patients with ischemic cardiomyopathy. In controls, NOX5 localized to the endothelium of a limited number of intramyocardial blood vessels and to a limited number of scattered cardiomyocytes. In infarcted hearts, NOX5 expression increased, especially in infarctions >12 hours, which manifested as an increase in NOX5-positive intramyocardial blood vessels, as well as in endothelium, smooth muscle, and cardiomyocytes. NOX5 was found in cardiomyocyte cytoplasm, plasma membrane, intercalated disks, and cross striations. Western blot analysis confirmed NOX5 expression in isolated human cardiomyocytes. For the first time to our knowledge, we demonstrate NOX5 expression in human intramyocardial blood vessels and cardiomyocytes, with significant increases in the affected myocardium after acute myocardial infarction.
Elsevier