Effects of glucose metabolism pathways on nuclear and cytoplasmic maturation of pig oocytes

• Published in: Scientific reports 2020-02, Vol.10 (1), p.2782-2782, Article 2782
• Main Authors: Wen, Jing, Wang, Guo-Liang, Yuan, Hong-Jie, Zhang, Jie, Xie, Hong-Li, Gong, Shuai, Han, Xiao, Tan, Jing-He
• Format: Article
• Language: English
• Subjects: 631/136; 631/45; 631/80; Animals; Cell differentiation; Cell Nucleus - metabolism; Coculture Techniques; Cumulus Cells - metabolism; Cytoplasm - metabolism; Electron transport; Enzymatic activity; Female; Gene silencing; Glucose; Glucose - metabolism; Glycolysis; Glycolysis - genetics; Humanities and Social Sciences; In Vitro Oocyte Maturation Techniques - methods; Lactic acid; Maturation; Metabolism; Metabolites; Mice; Mitochondria; Mitochondria - metabolism; multidisciplinary; Oocytes; Oocytes - growth & development; Oocytes - metabolism; Oxidation; Oxidation-Reduction; Pentose phosphate pathway; Pentose Phosphate Pathway - genetics; Pyruvic acid; Pyruvic Acid - metabolism; RNA-mediated interference; Science; Science (multidisciplinary); Swine
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-59709-6

The developmental competence of IVM porcine oocytes is still low compared with that in their in vivo counterparts. Although many studies reported effects of glucose metabolism (GM) on oocyte nuclear maturation, few reported on cytoplasmic maturation. Previous studies could not differentiate whether GM of cumulus cells (CCs) or that of cumulus-denuded oocytes (DOs) supported oocyte maturation. Furthermore, species differences in oocyte GM are largely unknown. Our aim was to address these issues by using enzyme activity inhibitors, RNAi gene silencing and special media that could support nuclear but not cytoplasmic maturation when GM was inhibited. The results showed that GM in CCs promoted pig oocyte maturation by releasing metabolites from both pentose phosphate pathway and glycolysis. Both pyruvate and lactate were transferred into pig DOs by monocarboxylate transporter and pyruvate was further delivered into mitochondria by mitochondrial pyruvate carrier in both pig DOs and CCs. In both pig DOs and CCs, pyruvate and lactate were utilized through mitochondrial electron transport and LDH-catalyzed oxidation to pyruvate, respectively. Pig and mouse DOs differed in their CC dependency for glucose, pyruvate and lactate utilization. While mouse DOs could not, pig DOs could use the lactate-derived pyruvate.