Generation, Release, and Uptake of the NAD Precursor Nicotinic Acid Riboside by Human Cells

• Published in: The Journal of biological chemistry Vol. 290; no. 45; pp. 27124 - 27137
• Main Authors: Kulikova, Veronika, Shabalin, Konstantin, Nerinovski, Kirill, Dölle, Christian, Niere, Marc, Yakimov, Alexander, Redpath, Philip, Khodorkovskiy, Mikhail, Migaud, Marie E., Ziegler, Mathias, Nikiforov, Andrey
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 06.11.2015; American Society for Biochemistry and Molecular Biology
• Subjects: 5'-Nucleotidase - metabolism; 5′-nucleotidase; Cytokines - metabolism; HEK293 Cells; Hep G2 Cells; Humans; Kinetics; Magnetic Resonance Spectroscopy; Metabolic Networks and Pathways; Metabolism; molecular cell biology; NAD - biosynthesis; Niacin - metabolism; Niacinamide - analogs & derivatives; Niacinamide - biosynthesis; Niacinamide - metabolism; nicotinamide; nicotinamide adenine dinucleotide (NAD); Nicotinamide Phosphoribosyltransferase - metabolism; nicotinic acid; nicotinic acid riboside; nucleoside/nucleotide metabolism; Pentosyltransferases - metabolism; Phosphorylation; Recombinant Proteins - metabolism; Ribonucleosides - biosynthesis; Ribonucleosides - metabolism; Signal Transduction; Substrate Specificity; molecular cell biology; nucleoside/nucleotide metabolism; 5′-nucleotidase; nicotinamide adenine dinucleotide (NAD); NAD biosynthesis; nicotinamide; nicotinic acid riboside; nicotinic acid
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M115.664458

NAD is essential for cellular metabolism and has a key role in various signaling pathways in human cells. To ensure proper control of vital reactions, NAD must be permanently resynthesized. Nicotinamide and nicotinic acid as well as nicotinamide riboside (NR) and nicotinic acid riboside (NAR) are the major precursors for NAD biosynthesis in humans. In this study, we explored whether the ribosides NR and NAR can be generated in human cells. We demonstrate that purified, recombinant human cytosolic 5′-nucleotidases (5′-NTs) CN-II and CN-III, but not CN-IA, can dephosphorylate the mononucleotides nicotinamide mononucleotide and nicotinic acid mononucleotide (NAMN) and thus catalyze NR and NAR formation in vitro. Similar to their counterpart from yeast, Sdt1, the human 5′-NTs require high (millimolar) concentrations of nicotinamide mononucleotide or NAMN for efficient catalysis. Overexpression of FLAG-tagged CN-II and CN-III in HEK293 and HepG2 cells resulted in the formation and release of NAR. However, NAR accumulation in the culture medium of these cells was only detectable under conditions that led to increased NAMN production from nicotinic acid. The amount of NAR released from cells engineered for increased NAMN production was sufficient to maintain viability of surrounding cells unable to use any other NAD precursor. Moreover, we found that untransfected HeLa cells produce and release sufficient amounts of NAR and NR under normal culture conditions. Collectively, our results indicate that cytosolic 5′-NTs participate in the conversion of NAD precursors and establish NR and NAR as integral constituents of human NAD metabolism. In addition, they point to the possibility that different cell types might facilitate each other's NAD supply by providing alternative precursors. Background: Nicotinamide riboside (NR) and nicotinic acid riboside (NAR) can serve as precursors of NAD in human cells. Results: Human cells generate and release NR and NAR. Conclusion: NR and NAR are authentic intermediates of human NAD metabolism. Significance: Different cell populations might support each other's NAD pools by providing ribosides as NAD precursors.