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Projekt Druckansicht

Die Rolle von NADPH-Oxidasen in der Multiplen Sklerose und ihrem Tiermodell der experimentellen autoimmunen Enzephalomyelitis

Antragstellerinnen / Antragsteller Dr. Kerstin Göbel; Professor Dr. Sven G. Meuth
Fachliche Zuordnung Molekulare und zelluläre Neurologie und Neuropathologie
Molekulare Biologie und Physiologie von Nerven- und Gliazellen
Förderung Förderung von 2015 bis 2019
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 276786445
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

Accumulating evidence suggest that oxidative stress plays a major role in the pathogenesis of MS, whereas a specific influence of oxidative stress on BBB dysfunction in MS was unclear so far. Here, we identify nicotinamide adenine dinucleotide phosphate (NADPH) oxidase type 4 (NOX4) as a specific and direct modulator of BBB integrity. Deficiency of NOX4 rendered mice more susceptible to experimental autoimmune encephalomyelitis (an animal model of MS) and was accompanied by a remarkable enhancement of BBB disruption and CNS inflammation. Interestingly, neither NOX1 nor NOX2 was involved in these processes. Murine and human in vitro analysis revealed that lack of NOX4 amplifies leukocyte trafficking via chemokine release by endothelial cells. Further, reduced endothelial NOX4 expression was found in CNS tissue of individuals suffering from MS indicating an important role of NOX4 also in humans. Our study demonstrates, for the first time, that NOX4 is an important and direct regulator of BBB integrity. NOX4 activation can decrease BBB damage and cell invasion during neuroinflammation and may offer a novel strategy for the treatment of MS.

Projektbezogene Publikationen (Auswahl)

 
 

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