Ziel
Nitric oxide (NO) is an essential signaling molecule for diverse physiological and disease processes. The current paradigm of NO regulation focuses at the level of nitric oxide synthase (NOS). However, the respective unique or combined genetic deficiencies of the NOS isoforms exhibit relatively modest phenotypes in mice. Moreover, approaches targeted at modulating NOS activities have not successfully translated into therapy. All NOSs isoforms use arginine as the sole substrate for NO production and interestingly, only one enzyme in mammals- argininosuccinic acid lyase (ASL) synthesizes endogenous arginine. In humans, ASL deficiency (ASLD) causes argininosuccinic aciduria, the second most common urea cycle disorder. In stark contrast to other urea cycle disorders, patients with ASLD show systemic and chronic features even with good metabolic control. We recently demonstrated a new structural requirement of ASL for maintenance of a NO synthetic complex necessary for generation of NO from both intracellular and extracellular sources of arginine. Thus, in the absence of ASL, there is decreased NO signaling. Importantly, we were able to translate our findings in a clinical therapeutic human context by supplementing an ASA patient with NO donors and improving his cardiovascular and neurocognitive functions. We now hypothesize that regulating ASL would allow us to characterize the cellular and molecular mechanisms underlying the NO flux at normal and pathological conditions, for therapeutic applications.
Using a novel conditional knockout model of Asl, we are now uniquely positioned to dissect the cellular contribution of NO metabolism to different disease pathogenesis. As a proof of concept, we will start by dissecting NO metabolism in the central nervous system at homeostasis and in acute and chronic brain injury. Undoubtedly, our results will provide a novel approach for the study of other NO related disorders, with therapeutic application.
Wissenschaftliches Gebiet
Aufforderung zur Vorschlagseinreichung
FP7-PEOPLE-2013-CIG
Andere Projekte für diesen Aufruf anzeigen
Finanzierungsplan
MC-CIG - Support for training and career development of researcher (CIG)Koordinator
7610001 Rehovot
Israel