4.7 Article

LDHA deficiency inhibits trophoblast proliferation via the PI3K/AKT/FOXO1/CyclinD1 signaling pathway in unexplained recurrent spontaneous abortion

Journal

FASEB JOURNAL
Volume 37, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1096/fj.202201219RR

Keywords

cleaved caspase-7; CyclinD1; LDHA; p-AKT

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Dysregulated trophoblast function, specifically related to lactate dehydrogenase A (LDHA) and the PI3K/AKT/FOXO1/CyclinD1 signaling pathway, may be involved in the development of pregnancy-associated complications such as unexplained recurrent spontaneous abortion (URSA). In this study, the authors found that reduced LDHA levels in the placental villus of URSA patients contributed to G0/G1 phase arrest and increased apoptosis in trophoblast cells. Furthermore, LDHA knockdown affected the phosphorylation levels of PI3K, AKT, and FOXO1, resulting in downregulation of CyclinD1. The findings highlight a novel regulatory pathway for trophoblast cell cycle and proliferation.
Dysregulated trophoblast proliferation, invasion, and apoptosis may cause several pregnancy-associated complications, such as unexplained recurrent spontaneous abortion (URSA). Recent studies have shown that metabolic abnormalities, including glycolysis inhibition, may dysregulate trophoblast function, leading to URSA. However, the underlying mechanisms remain unclear. Herein, we found that lactate dehydrogenase A (LDHA), a key enzyme in glycolysis, was significantly reduced in the placental villus of URSA patients. The human trophoblast cell line HTR-8/SVneo was used to investigate the possible LDHA-mediated regulation of trophoblast function. LDHA knockdown in HTR-8/SVneo cells induced G0/G1 phase arrest and increased apoptosis, whereas LDHA overexpression reversed these effects. Next, RNA sequencing combined with Kyoto Encyclopedia of Genes and Genomes analysis demonstrated that the PI3K/AKT signaling pathway is potentially affected by downstream genes of LDHA. Especially, we found that LDHA knockdown decreased the phosphorylation levels of PI3K, AKT, and FOXO1, resulting in a significant downregulation of CyclinD1. In addition, treatment with an AKT inhibitor or FOXO1 inhibitor also verified that the PI3K/AKT/FOXO1 signaling pathway influenced the gene expression of CyclinD1 in trophoblast. Moreover, p-AKT expression correlated positively with LDHA expression in syncytiotrophoblasts and extravillous trophoblasts in first-trimester villus. Collectively, this study revealed a new regulatory pathway for LDHA/PI3K/AKT/FOXO1/CyclinD1 in the trophoblast cell cycle and proliferation.

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