首页> 外文期刊>Placenta >Fatty acids alter glycerolipid metabolism and induce lipid droplet formation, syncytialisation and cytokine production in human trophoblasts with minimal glucose effect or interaction.
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Fatty acids alter glycerolipid metabolism and induce lipid droplet formation, syncytialisation and cytokine production in human trophoblasts with minimal glucose effect or interaction.

机译:脂肪酸以最小的葡萄糖作用或相互作用,改变人滋养细胞的甘油脂代谢并诱导脂质液滴形成,合胞体化和细胞因子产生。

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摘要

The diabetic pregnancy is characterized by maternal hyperglycaemia and dyslipidaemia, such that placental trophoblast cells are exposed to both. The objective was to determine the effects of hyperglycaemia, elevated non-esterified fatty acids (NEFA) and their interactions on trophoblast cell metabolism and function. Trophoblasts were isolated from normal term human placentas and established in culture for 16 h prior to experiments. Glucose utilisation, fatty acid oxidation and fatty acid esterification were determined using radiolabelled metabolic tracer methodology at various glucose and NEFA concentrations. Trophoblast lipid droplet formation including adipophilin mRNA expression, viability, apoptosis, syncytialisation, secretion of hormones and pro-inflammatory cytokines were also assessed. Glucose utilisation via glycolysis was near maximal at the low physiological glucose concentration of 4mM; whereas NEFA esterification into triacylglycerol and diacylglycerol increased linearly with increasing NEFA concentrations without evidence of plateau. Culture of trophoblasts in 0.25 mM NEFA for 24h upregulated fatty acid esterification processes, inhibited fatty acid oxidation, inhibited glycerol release (a marker of lipolysis) and promoted adipophilin and lipid droplet formation, all consistent with upregulation of fatty acid storage and buffering capacity. NEFA also promoted trophoblast syncytialisation and TNFalpha, IL-1beta, IL-6 and IL-10 production without effects on cell viability, apoptosis or hormone secretion. Hyperglycaemia caused intracellular glycogen accumulation and reduced lipid droplet formation, but had no other effects on trophoblast metabolism or function. NEFA have effects on trophoblast metabolism and function, mostly independent of glucose, that may have protective as well as pathophysiological roles in pregnancies complicated by diabetes and/or obesity.
机译:糖尿病妊娠的特征在于母体高血糖症和血脂异常,使得胎盘滋养层细胞暴露于这两种情况。目的是确定高血糖,升高的非酯化脂肪酸(NEFA)及其相互作用对滋养层细胞代谢和功能的影响。从正常人胎盘中分离滋养细胞,并在实验前培养16 h。使用放射性标记的代谢示踪剂方法在各种葡萄糖和NEFA浓度下测定葡萄糖利用,脂肪酸氧化和脂肪酸酯化。还评估了滋养层脂质小滴的形成,包括脂肪蛋白mRNA的表达,生存力,凋亡,合胞体化,激素分泌和促炎细胞因子。在4mM的低生理葡萄糖浓度下,通过糖酵解作用的葡萄糖利用率接近最大。而NEFA酯化成三酰基甘油和二酰基甘油的浓度随NEFA浓度的增加呈线性增加,而没有平台期的迹象。在0.25 mM NEFA中培养滋养层细胞24小时可上调脂肪酸酯化过程,抑制脂肪酸氧化,抑制甘油释放(脂解作用的标志)并促进脂肪亲脂和脂质滴的形成,所有这些都与脂肪酸储存和缓冲能力的上调一致。 NEFA还促进了滋养细胞的合胞作用和TNFalpha,IL-1beta,IL-6和IL-10的产生,而对细胞生存力,细胞凋亡或激素分泌没有影响。高血糖症引起细胞内糖原积累并减少脂质滴形成,但对滋养细胞代谢或功能没有其他影响。 NEFA对滋养细胞的代谢和功能有影响,大部分与葡萄糖无关,在患有糖尿病和/或肥胖症的孕妇中可能具有保护作用以及病理生理作用。

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