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Degradation of phosphate polymer polyP enhances lactic fermentation in mice

In bacteria, a polymer of inorganic phosphate (Pi) (inorganic polyphosphate; polyP) is enzymatically produced and consumed as an alternative phosphate donor for adenosine triphosphate (ATP) production to protect against nutrient starvation. In vertebrates, polyP has been dismissed as a “molecular fo...

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Published in:Genes to cells : devoted to molecular & cellular mechanisms 2018-10, Vol.23 (10), p.904-914
Main Authors: Nakamura, Akihiro, Kawano, Natsuko, Motomura, Kei, Kuroda, Akio, Sekiguchi, Kiyoshi, Miyado, Mami, Kang, Woojin, Miyamoto, Yoshitaka, Hanai, Maito, Iwai, Maki, Yamada, Mitsutoshi, Hamatani, Toshio, Saito, Takakazu, Saito, Hidekazu, Tanaka, Mamoru, Umezawa, Akihiro, Miyado, Kenji
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Language:English
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Summary:In bacteria, a polymer of inorganic phosphate (Pi) (inorganic polyphosphate; polyP) is enzymatically produced and consumed as an alternative phosphate donor for adenosine triphosphate (ATP) production to protect against nutrient starvation. In vertebrates, polyP has been dismissed as a “molecular fossil” due to the lack of any known physiological function. Here, we have explored its possible role by producing transgenic (TG) mice widely expressing Saccharomyces cerevisiae exopolyphosphatase 1 (ScPPX1), which catalyzes hydrolytic polyP degradation. TG mice were produced and displayed reduced mitochondrial respiration in muscles. In female TG mice, the blood concentration of lactic acid was enhanced, whereas ATP storage in liver and brain tissues was reduced significantly. Thus, we suggested that the elongation of polyP reduces the intracellular Pi concentration, suppresses anaerobic lactic acid production, and sustains mitochondrial respiration. Our results provide an insight into the physiological role of polyP in mammals, particularly in females. Schematic model of enhanced lactic fermentation by polyP degradation. PolyP degradation enhances lactic fermentation linked with ATP production, resulting in the reduction of ATP production in mitochondria.
ISSN:1356-9597
1365-2443
DOI:10.1111/gtc.12639