The Secret Life of NAD+: An Old Metabolite Controlling New Metabolic Signaling Pathways
Top Cited Papers
Open Access
- 1 April 2010
- journal article
- review article
- Published by The Endocrine Society in Endocrine Reviews
- Vol. 31 (2), 194-223
- https://doi.org/10.1210/er.2009-0026
Abstract
A century after the identification of a coenzymatic activity for NAD+, NAD+ metabolism has come into the spotlight again due to the potential therapeutic relevance of a set of enzymes whose activity is tightly regulated by the balance between the oxidized and reduced forms of this metabolite. In fact, the actions of NAD+ have been extended from being an oxidoreductase cofactor for single enzymatic activities to acting as substrate for a wide range of proteins. These include NAD+-dependent protein deacetylases, poly(ADP-ribose) polymerases, and transcription factors that affect a large array of cellular functions. Through these effects, NAD+ provides a direct link between the cellular redox status and the control of signaling and transcriptional events. Of particular interest within the metabolic/endocrine arena are the recent results, which indicate that the regulation of these NAD+-dependent pathways may have a major contribution to oxidative metabolism and life span extension. In this review, we will provide an integrated view on: 1) the pathways that control NAD+ production and cycling, as well as its cellular compartmentalization; 2) the signaling and transcriptional pathways controlled by NAD+; and 3) novel data that show how modulation of NAD+-producing and -consuming pathways have a major physiological impact and hold promise for the prevention and treatment of metabolic disease.Keywords
This publication has 255 references indexed in Scilit:
- A continuous microplate assay for sirtuins and nicotinamide-producing enzymesAnalytical Biochemistry, 2009
- SIRT5 Deacetylates Carbamoyl Phosphate Synthetase 1 and Regulates the Urea CycleCell, 2009
- Biochemical characterization, localization, and tissue distribution of the longer form of mouse SIRT3Protein Science, 2009
- Concurrent regulation of AMP-activated protein kinase and SIRT1 in mammalian cellsBiochemical and Biophysical Research Communications, 2008
- AMPK and PPARδ Agonists Are Exercise MimeticsCell, 2008
- The NAD+-Dependent Deacetylase SIRT1 Modulates CLOCK-Mediated Chromatin Remodeling and Circadian ControlCell, 2008
- SIRT1 Regulates Circadian Clock Gene Expression through PER2 DeacetylationCell, 2008
- Transcriptional targets of sirtuins in the coordination of mammalian physiologyCurrent Opinion in Cell Biology, 2008
- Nutrient-Sensitive Mitochondrial NAD+ Levels Dictate Cell SurvivalCell, 2007
- The Plasticity of Aging: Insights from Long-Lived MutantsCell, 2005