Mechanism of neutrophil extracellular traps generation and their role in trophoblasts apoptosis in gestational diabetes mellitus

• Published in: Cellular signalling 2021-12, Vol.88, p.110168-110168, Article 110168
• Main Authors: Shen, Di, Lu, Yuan, Li, Guangzhen, Hu, Min, Li, Shanling, Ju, Hui, Zhang, Meihua, Wang, Xietong
• Format: Article
• Language: English
• Subjects: Adiponectin; Apoptosis; Diabetes, Gestational - metabolism; Extracellular Traps - metabolism; Female; Gestational diabetes mellitus; Humans; NADPH Oxidases - metabolism; Neutrophil extracellular traps; Neutrophils - metabolism; Placenta - metabolism; Pregnancy; Reactive Oxygen Species - metabolism; Trophoblast; Trophoblasts - metabolism
• ISSN: 0898-6568; 1873-3913
• DOI: 10.1016/j.cellsig.2021.110168

Gestational diabetes mellitus (GDM) is a metabolic syndrome occurring in pregnant women and increases the risk of placental dysplasia. Neutrophil extracellular traps (NETs) may play a critical role in placental dysplasia. NETosis (neutrophil cell death by NET release) depends on NADPH/ROS pathway. In view of the adiponectin which is widely believed to be reduced in GDM patients suppresses NADPH oxidase and ROS generation of neutrophil. We speculate that increased NET release is associated with hypoadiponectinemia. Trophoblast apoptosis is significantly increased in GDM patients, but it is not clear whether NETs promotes cell apoptosis. This study aims to reveal the mechanism of Neutrophil Extracellular Traps generation and their role in trophoblast apoptosis in Gestational Diabetes Mellitus. We investigated the generation of NETs by cell-free DNA (cf-DNA) quantification, live-cell imaging, and reactive oxygen species (ROS) measurement. ERK1/2 and p38 MAPK signalling pathway proteins were detected by western blotting. The Cell Counting Kit-8 (CCK-8) assay, flow cytometry, and western blotting were performed to explore the effects of NETs on trophoblast apoptosis. We found that adiponectin inhibited NET release by suppressing ROS production, and p38 MAPK and ERK1/2 proteins were involved in the process. Further, NETs promoted trophoblast apoptosis by activating the ROS-dependent mitochondrial pathway, which is mediated by ERK1/2 signalling. The current study demonstrated that hypoadiponectinemia is the cause of NETs formation and NETs promoting trophoblast apoptosis. •We found that adiponectin inhibited NET release by suppressing ROS production, and p38 MAPK and ERK1/2 proteins were involved in the process. Further, NETs promoted trophoblast apoptosis by activating the ROS-dependent mitochondrial pathway, which is mediated by ERK1/2 signalling.•This study elucidates the mechanism of NETS generation in gestational diabetes and the effect of NET on trophoblasts apoptosis. The association between hypoadiponectin, NETs, and trophoblast apoptosis in GDM were explored.