There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
Abstract
Mistakenly thought to be the consequence of oxygen lack in contracting skeletal muscle
we now know that the L-enantiomer of the lactate anion is formed under fully aerobic
conditions and is utilized continuously in diverse cells, tissues, organs and at the
whole-body level. By shuttling between producer (driver) and consumer (recipient)
cells lactate fulfills at least three purposes: 1] a major energy source for mitochondrial
respiration; 2] the major gluconeogenic precursor; and 3] a signaling molecule. Working
by mass action, cell redox regulation, allosteric binding, and reprogramming of chromatin
by lactylation of lysine residues on histones, lactate has major influences in energy
substrate partitioning. The physiological range of tissue [lactate] is 0.5–20 mM and
the cellular Lactate/Pyruvate ratio (L/P) can range from 10 to >500; these changes
during exercise and other stress-strain responses dwarf other metabolic signals in
magnitude and span. Hence, lactate dynamics have rapid and major short- and long-term
effects on cell redox and other control systems. By inhibiting lipolysis in adipose
via HCAR-1, and muscle mitochondrial fatty acid uptake via malonyl-CoA and CPT1, lactate
controls energy substrate partitioning. Repeated lactate exposure from regular exercise
results in major effects on the expression of regulatory enzymes of glycolysis and
mitochondrial respiration. Lactate is the fulcrum of metabolic regulation in vivo.
We have identified a 50-nucleotide enhancer from the human erythropoietin gene 3'-flanking sequence which can mediate a sevenfold transcriptional induction in response to hypoxia when cloned 3' to a simian virus 40 promoter-chloramphenicol acetyltransferase reporter gene and transiently expressed in Hep3B cells. Nucleotides (nt) 1 to 33 of this sequence mediate sevenfold induction of reporter gene expression when present in two tandem copies compared with threefold induction when present in a single copy, suggesting that nt 34 to 50 bind a factor which amplifies the induction signal. DNase I footprinting demonstrated binding of a constitutive nuclear factor to nt 26 to 48. Mutagenesis studies revealed that nt 4 to 12 and 19 to 23 are essential for induction, as substitutions at either site eliminated hypoxia-induced expression. Electrophoretic mobility shift assays identified a nuclear factor which bound to a probe spanning nt 1 to 18 but not to a probe containing a mutation which eliminated enhancer function. Factor binding was induced by hypoxia, and its induction was sensitive to cycloheximide treatment. We have thus defined a functionally tripartite, 50-nt hypoxia-inducible enhancer which binds several nuclear factors, one of which is induced by hypoxia via de novo protein synthesis.
Once thought to be the consequence of oxygen lack in contracting skeletal muscle, the glycolytic product lactate is formed and utilized continuously in diverse cells under fully aerobic conditions. 'Cell-cell' and 'intracellular lactate shuttle' concepts describe the roles of lactate in delivery of oxidative and gluconeogenic substrates as well as in cell signalling. Examples of the cell-cell shuttles include lactate exchanges between between white-glycolytic and red-oxidative fibres within a working muscle bed, and between working skeletal muscle and heart, brain, liver and kidneys. Examples of intracellular lactate shuttles include lactate uptake by mitochondria and pyruvate for lactate exchange in peroxisomes. Lactate for pyruvate exchanges affect cell redox state, and by itself lactate is a ROS generator. In vivo, lactate is a preferred substrate and high blood lactate levels down-regulate the use of glucose and free fatty acids (FFA). As well, lactate binding may affect metabolic regulation, for instance binding to G-protein receptors in adipocytes inhibiting lipolysis, and thus decreasing plasma FFA availability. In vitro lactate accumulation upregulates expression of MCT1 and genes coding for other components of the mitochondrial reticulum in skeletal muscle. The mitochondrial reticulum in muscle and mitochondrial networks in other aerobic tissues function to establish concentration and proton gradients necessary for cells with high mitochondrial densities to oxidize lactate. The presence of lactate shuttles gives rise to the realization that glycolytic and oxidative pathways should be viewed as linked, as opposed to alternative, processes, because lactate, the product of one pathway, is the substrate for the other.
scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.