Open AccessCellular Compartmentation and the Redox/Nonredox Functions of NAD+
Author(s) -
Chaitanya A. Kulkarni,
Paul S. Brookes
Publication year - 2019
Publication title -
antioxidants and redox signaling
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.277
H-Index - 190
eISSN - 1557-7716
pISSN - 1523-0864
DOI - 10.1089/ars.2018.7722
Subject(s) - nad+ kinase , cofactor , redox , nicotinamide adenine dinucleotide , biochemistry , enzyme , cytosol , cellular compartment , biology , metabolism , microbiology and biotechnology , compartment (ship) , glycerol 3 phosphate dehydrogenase , poly adp ribose polymerase , mitochondrion , cell , chemistry , polymerase , oceanography , organic chemistry , geology
Significance: Nicotinamide adenine dinucleotide (NAD + ) spans diverse roles in biology, serving as both an important redox cofactor in metabolism and a substrate for signaling enzymes that regulate protein post-translational modifications (PTMs). Critical Issues: Although the interactions between these different roles of NAD + (and its reduced form NADH) have been considered, little attention has been paid to the role of compartmentation in these processes. Specifically, the role of NAD + in metabolism is compartment specific ( e.g. , mitochondrial vs. cytosolic), affording a very different redox landscape for PTM-modulating enzymes such as sirtuins and poly(ADP-ribose) polymerases in different cell compartments. In addition, the orders of magnitude differences in expression levels between NAD + -dependent enzymes are often not considered when assuming the effects of bulk changes in NAD + levels on their relative activities. Recent Advances: In this review, we discuss the metabolic, nonmetabolic, redox, and enzyme substrate roles of cellular NAD + , and the recent discoveries regarding the interplay between these roles in different cell compartments. Future Directions: Therapeutic implications for the compartmentation and manipulation of NAD + biology are discussed. Antioxid. Redox Signal. 31, 623-642.