Warburg-like Glycolysis and Lactate Shuttle in Mouse Decidua during Early Pregnancy

• Published in: The Journal of biological chemistry Vol. 290; no. 35; pp. 21280 - 21291
• Main Authors: Zuo, Ru-Juan, Gu, Xiao-Wei, Qi, Qian-Rong, Wang, Tong-Song, Zhao, Xu-Yu, Liu, Ji-Long, Yang, Zeng-Ming
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 28.08.2015; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; carbohydrate metabolism; Cells, Cultured; decidualization; Developmental Biology; Endometrium - cytology; Endometrium - physiology; Female; Glycolysis; Hif1α; Hypoxia-Inducible Factor 1, alpha Subunit - metabolism; lactate flux; Lactic Acid - metabolism; Mice - physiology; Pregnancy; Pregnancy, Animal - physiology; progesterone; Progesterone - metabolism; reproduction; Stromal Cells - cytology; Stromal Cells - metabolism; Warburg effect; Warburg-like glycolysis; Hif1α; carbohydrate metabolism; Warburg-like glycolysis; glycolysis; pregnancy; progesterone; decidualization; lactate flux; reproduction; Warburg effect
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M115.656629

Decidualization is an essential process of maternal endometrial stromal cells to support pregnancy. Although it is known that enhanced glucose influx is critical for decidualization, the underlying mechanism in regulating glucose metabolism in decidua remains insufficiently understood. Here, we demonstrate that aerobic glycolysis-related genes and factors are all substantially induced during decidualization, indicating the existence of Warburg-like glycolysis in decidua. In vitro, progesterone activates hypoxia-inducible factor 1α (Hif1α) and c-Myc through Pi3k-Akt signaling pathway to maintain aerobic glycolysis in decidualizing cells. Knocking down of pyruvate kinase M2 (Pkm2) attenuates the induction of decidual marker gene. Decidual formation in vivo is also impaired by glycolysis inhibitor 3-bromopyruvate. Besides, lactate exporter monocarboxylate transporter 4 (Mct4) is induced in newly formed decidual cells, whereas lactate importer Mct1 and proliferation marker Ki-67 are complementarily located in the surrounding undifferentiated cells, which are supposed to consume lactate for proliferation. Hif1α activation is required for lactate-dependent proliferation of the undifferentiated cells. Inhibition of lactate flux leads to compromised decidualization and decelerated lactate-dependent proliferation. In summary, we reveal that Warburg-like glycolysis and local lactate shuttle are activated in decidua and play important roles for supporting early pregnancy. Background: Carbohydrate metabolism during decidualization is unknown. Results: Decidual cells undergo glycolysis upon progesterone signals, and the undifferentiated stromal cells consume lactate for proliferation. Inhibition of glycolysis or lactate flux could compromise decidual development. Conclusion: Warburg-like glycolysis and lactate communication play critical roles during decidualization. Significance: Our study will be valuable for understanding the mechanism underlying decidualization.