Journal Article

Boosting NAD+ blunts TLR4-induced type I IFN in control and systemic lupus erythematosus monocytes

Wu, Kaiyuan, Singh, Komudi, Meadows, Allison M., Sack, Michael N., Tian, Rong, Kaplan, Mariana J., Bley, Maximilian, Pirooznia, Mehdi, Wu, Jing, Lin, Amy, Shing, Vivian, Blanco, Luz P., Hassanzadeh, Shahin, Huffstutler, Rebecca D., Schmidt, Mark S., Brenner, Charles

2022

Overview

BACKGROUNDFasting and NAD+-boosting compounds, including NAD+ precursor nicotinamide riboside (NR), confer antiinflammatory effects. However, the underlying mechanisms and therapeutic potential are incompletely defined.METHODSWe explored the underlying biology in myeloid cells from healthy volunteers following in vivo placebo or NR administration and subsequently tested the findings in vitro in monocytes extracted from patients with systemic lupus erythematosus (SLE).RESULTSRNA-Seq of unstimulated and LPS-activated monocytes implicated NR in the regulation of autophagy and type I IFN signaling. In primary monocytes, NR blunted LPS-induced IFN-β production, and genetic or pharmacological disruption of autophagy phenocopied this effect. Given that NAD+ is a coenzyme in oxidoreductive reactions, metabolomics was performed and identified that NR increased the inosine level. Inosine supplementation similarly blunted autophagy and IFN-β release. Finally, because SLE exhibits type I IFN dysregulation, we assessed the NR effect on monocytes from patients with SLE and found that NR reduced autophagy and IFN-β release.CONCLUSIONWe conclude that NR, in an NAD+-dependent manner and in part via inosine signaling, mediated suppression of autophagy and attenuated type I IFN in myeloid cells, and we identified NR as a potential adjunct for SLE management.TRIAL REGISTRATIONClinicalTrials.gov registration numbers NCT02812238, NCT00001846, and NCT00001372.FUNDINGThis work was supported by the NHLBI and NIAMS Intramural Research divisions.

• Publisher: American Society for Clinical Investigation
• Subject: Alzheimer's disease / Autophagy / Biomedical research / Clinical Medicine / Clinical Studies as Topic / Cytokines / Gene expression / Genetic engineering / Homeostasis / Humans / Inflammation / Inosine / Interferon-beta / Kinases / Lipopolysaccharides / Lupus / Lupus Erythematosus, Systemic / Metabolism / Metabolomics / Monocytes / Myeloid cells / NAD / Niacinamide / Phosphorylation / Supplements / Systemic lupus erythematosus / TLR4 protein / Toll-Like Receptor 4 / Toll-like receptors / β-Interferon