Nox4 supports proper capillary growth in exercise and retina neo-vascularization
| Autor: | Christoph Kruse, Juri Vogel, Katrin Schröder, Min Zhang |
|---|---|
| Rok vydání: | 2015 |
| Předmět: |
medicine.medical_specialty
Retina NADPH oxidase biology urogenital system Physiology Angiogenesis NOX4 medicine.disease Vascular remodelling in the embryo Vascular endothelial growth factor chemistry.chemical_compound medicine.anatomical_structure Endocrinology chemistry Internal medicine Knockout mouse cardiovascular system medicine biology.protein Retinopathy |
| Zdroj: | The Journal of Physiology. 593:2145-2154 |
| ISSN: | 0022-3751 |
| DOI: | 10.1113/jphysiol.2014.284901 |
| Popis: | Key points We provide evidence for two distinct functions of the NADPH oxidase Nox4 in angiogenesis using Nox4 knockout mice. First, Nox4 maintains vascular endothelial growth factor expression and prevents an increase in angiopoietin 1 expression, thereby contributing to angiogenesis in exercise. Second, deletion of Nox4, via an enhanced angiopoietin 1 expression, contributes to stabilization of new formed vessels and prevents an exacerbated neo-angiogenesis in oxygen-induced retinopathy. By contrast, Nox4 does not influence developmental angiogenesis. Abstract By producing H2O2, the NADPH oxidase Nox4 is involved in hypoxia-induced angiogenesis, as present in vascular remodelling of the hypertrophic heart or blood flow recovery after hind limb ischaemia. In the present study, we hypothesized that Nox4 contributes to proper capillary growth in the retina and in exercised muscles and investigated this in wild-type and Nox4−/− mice. Exercise, as induced by voluntary running in a running wheel or forced running on a treadmill, stimulated capillary growth in wild-type but not Nox4−/− mice. As an underlying mechanism, we identified both vascular endothelial growth factor (VEGF) expression to be reduced and angiopoietin 1 (Ang1) expression to be increased in response to Nox4 knockout. To differentiate the two factors, oxygen-induced retinopathy was investigated. In this model, deletion of Nox4 protected from neo-angiogenesis and stabilized the network of regrown vessels, which is a typical feature of Ang1. However the angiogenesis in the developing retina was similar between Nox4−/− and wild-type mice. Thus, Nox4 contributes to exercise- and hypoxia-induced angiogenesis through a dual mechanism of maintaining VEGF and preventing Ang-1 expression, whereas the developmental angiogenesis is Nox4 independent. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Plný text