Nicotinamide riboside kinases regulate skeletal muscle fiber-type specification and are rate-limiting for metabolic adaptations during regeneration

Abstract

Nicotinamide riboside kinases (NRKs) control the conversion of dietary Nicotinamide Riboside (NR) to NAD+, but little is known about their contribution to endogenous NAD+ turnover and muscle plasticity during skeletal muscle growth and remodeling. Using NRK1/2 double KO (NRKdKO) mice, we investigated the influence of NRKs on NAD+ metabolism and muscle homeostasis, and on the response to neurogenic muscle atrophy and regeneration following muscle injury. Muscles from NRKdKO animals have altered nicotinamide (NAM) salvage and a decrease in mitochondrial content. In single myonuclei RNAseq of skeletal muscle, NRK2 mRNA expression is restricted to type IIx muscle fibers, and perturbed NAD+ turnover and mitochondrial metabolism shifts the fiber type composition of NRKdKO muscle to fast glycolytic IIB fibers. NRKdKO does not influence muscle atrophy during denervation but alters muscle repair after myofiber injury. During regeneration, muscle stem cells (MuSCs) from NRKdKO animals hyper-proliferate but fail to differentiate. NRKdKO also alters the recovery of NAD+ during muscle regeneration as well as mitochondrial adaptations and extracellular matrix remodeling required for tissue repair. These metabolic perturbations result in a transient delay of muscle regeneration which normalizes during myofiber maturation at late stages of regeneration via over-compensation of anabolic IGF1-Akt signaling. Altogether, we demonstrate that NAD+ synthesis controls mitochondrial metabolism and fiber type composition via NRK1/2 and is rate-limiting for myogenic commitment and mitochondrial maturation during skeletal muscle repair.

NAD+ repletion with niacin counteracts cancer cachexia

“…A previous mouse study demonstrated that NR conversion to NAD + via NRKs is active in healthy muscle and NRKs regulate metabolic adaptations upon muscle regeneration 24 . However, Nrk2 plays a redundant role in basal muscle NAD + biosynthesis [24][25][26] .…”

“…A previous mouse study demonstrated that NR conversion to NAD + via NRKs is active in healthy muscle and NRKs regulate metabolic adaptations upon muscle regeneration 24 . However, Nrk2 plays a redundant role in basal muscle NAD + biosynthesis [24][25][26] . Interestingly, Nrk2 is typically upregulated during metabolic energy stress and NAD + deficiency to support NAD + production [26][27][28] .…”

Nicotinamide Riboside, a Promising Vitamin B3 Derivative for Healthy Aging and Longevity: Current Research and Perspectives

“…Numerous preclinical studies have suggested that NR and NMN dietary supplements increase NAD + levels in the skeletal muscle and help protect musculoskeletal system from age-related metabolic dysfunction. NAD + biosynthesis pathways/homeostasis and its bioavailability in skeletal muscle cells are influenced by NAM phosphoribosyltransferase (NAMPT), NRK1, and NRK2 enzymes [ 118 , 119 ]. After the application of NRS in hexose-6-phosphate dehydrogenase KO (H6PDKO) mice, NAD + /NADH ratio was elevated but without any effect on insulin sensitivity, MT respiratory dysfunctions (MT acylcarnitine), acetyl coenzyme A metabolism and endoplasmic reticulum OXS [ 120 , 121 ].…”

Biosynthesis of Nicotinamide Mononucleotide: Current Metabolic Engineering Strategies, Challenges, and Prospects

“…NMN is synthesized from NR via NRK-mediated phosphorylation, bypassing the need for NAMPT [15]. Mammals possess specific NRKs that function to synthesize NAD + via NMN in addition to the well-known pathways through NaMN [26].…”