Autor: |
Shao-Liang, Yang, Hai-Xia, Tan, Zhen-Zhen, Lai, Hai-Yan, Peng, Hui-Li, Yang, Qiang, Fu, Hai-Yan, Wang, Da-Jin, Li, Ming-Qing, Li |
Rok vydání: |
2022 |
Předmět: |
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Zdroj: |
Cellular and molecular life sciences : CMLS. 79(12) |
ISSN: |
1420-9071 |
Popis: |
Deficiency of decidual NK (dNK) cell number and function has been widely regarded as an important cause of spontaneous abortion. However, the metabolic mechanism underlying the crosstalk between dNK cells and embryonic trophoblasts during early pregnancy remains largely unknown. Here, we observed that enriched glutamine and activated glutaminolysis in dNK cells contribute to trophoblast invasion and embryo growth by insulin-like growth factor-1 (IGF-1) and growth differentiation factor-15 (GDF-15) secretion. Mechanistically, these processes are dependent on the downregulation of EGLN1-HIF-1α mediated by α-ketoglutarate (α-KG). Blocking glutaminolysis with the GLS inhibitor BPTES or the glutamate dehydrogenase inhibitor EGCG leads to early embryo implantation failure, spontaneous abortion and/or fetal growth restriction in pregnant mice with impaired trophoblast invasion. Additionally, α-KG supplementation significantly alleviated pregnancy loss mediated by defective glutaminolysis in vivo, suggesting that inactivated glutamine/α-ketoglutarate metabolism in dNK cells impaired trophoblast invasion and induced pregnancy loss. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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