Stoikou Maria, Grimolizzi Franco, Giaglis Stavros, Schäfer Günther, van Breda Shane Vontelin, Hoesli Irene Mathilde, Lapaire Olav, Huhn Evelyn A, Hasler Paul, Rossi Simona W, Hahn Sinuhe
Department of Biomedicine, University of Basel, University Hospital of Basel, Basel, Switzerland.
Department Clinical Sciences, Polytechnic University Marche, Ancona, Italy.
Front Immunol. 2017 Jun 14;8:702. doi: 10.3389/fimmu.2017.00702. eCollection 2017.
Gestational diabetes mellitus (GDM) is a unique form of glucose intolerance, in that it is transient and solely occurs in pregnancy. Pregnancies with GDM are at high risk of developing preeclampsia (PE), a leading cause of fetal and maternal morbidity or mortality. Since PE is associated with excessive activation of circulatory neutrophils and occurrence of neutrophil extracellular traps (NETs) in affected placentae, we examined these features in cases with GDM, as this could be a feature linking the two conditions. Our data indicate that neutrophil activity is indeed altered in GDM, exhibiting pronounced activation and spontaneous generation of NETs by isolated neutrophils in culture. In this manner, GDM may similarly affect neutrophil behavior and NET formation as witnessed in other forms of diabetes, with the addition of the physiological changes mediated by pregnancy. Since circulatory TNF-α levels are elevated in cases with GDM, a feature also observed in this study, we examined whether this pro-inflammatory cytokine contributed to neutrophil activation. By using infliximab, a clinically utilized TNF-α antagonist, we observed that the pro-NETotic effect of GDM sera was significantly reduced. We also detected pronounced neutrophil infiltrates in placentae from GDM cases. The occurrence of NETs in these tissues is suggested by the extracellular co-localization of citrullinated histones and myeloperoxidase. In addition, elevated neutrophil elastase (NE) mRNA and active enzymatic protein were also detected in such placentae. This latter finding could be important in the context of previous studies in cancer or diabetes model systems, which indicated that NE liberated from infiltrating neutrophils enters surrounding cells, altering cell signaling by the degradation of IRS1. These findings could potentiate the underlying inflammatory response process in GDM and possibly open an avenue for the therapeutic interventions in gestational hyperglycemia.
妊娠期糖尿病(GDM)是一种独特的葡萄糖不耐受形式,因为它是短暂性的,仅发生在孕期。患有GDM的孕妇发生先兆子痫(PE)的风险很高,PE是导致胎儿和母亲发病或死亡的主要原因。由于PE与循环中性粒细胞过度活化以及受影响胎盘中性粒细胞胞外陷阱(NETs)的出现有关,我们研究了GDM病例中的这些特征,因为这可能是将这两种情况联系起来的一个特征。我们的数据表明,GDM中中性粒细胞活性确实发生了改变,在培养中分离的中性粒细胞表现出明显的活化和NETs的自发产生。通过这种方式,GDM可能与其他形式的糖尿病一样影响中性粒细胞行为和NET形成,同时还伴有妊娠介导的生理变化。由于GDM病例中循环肿瘤坏死因子-α(TNF-α)水平升高,本研究也观察到了这一特征,我们研究了这种促炎细胞因子是否促成了中性粒细胞活化。通过使用临床应用的TNF-α拮抗剂英夫利昔单抗,我们观察到GDM血清的促NET形成作用显著降低。我们还在GDM病例的胎盘中检测到明显的中性粒细胞浸润。瓜氨酸化组蛋白和髓过氧化物酶在细胞外的共定位提示了这些组织中NETs的存在。此外,在这些胎盘中还检测到中性粒细胞弹性蛋白酶(NE)mRNA和活性酶蛋白升高。后一发现在前癌症或糖尿病模型系统的研究背景下可能很重要,这些研究表明,浸润的中性粒细胞释放的NE进入周围细胞,通过降解胰岛素受体底物1(IRS1)改变细胞信号传导。这些发现可能会增强GDM潜在的炎症反应过程,并可能为妊娠期高血糖的治疗干预开辟一条途径。