Department of Pathology and Immunology, University of Geneva School of Medicine, Geneva, Switzerland.
Department of Cell Physiology and Metabolism, University of Geneva School of Medicine, Geneva, Switzerland.
Sci Rep. 2023 Sep 8;13(1):14805. doi: 10.1038/s41598-023-42072-7.
Stimulation of glucose uptake in response to ischemic metabolic stress is important for cardiomyocyte function and survival. Chronic exposure of cardiomyocytes to fatty acids (FA) impairs the stimulation of glucose uptake, whereas induction of lipid droplets (LD) is associated with preserved glucose uptake. However, the mechanisms by which LD induction prevents glucose uptake impairment remain elusive. We induced LD with either tetradecanoyl phorbol acetate (TPA) or 5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside (AICAR). Triacylglycerol biosynthesis enzymes were inhibited in cardiomyocytes exposed to FA ± LD inducers, either upstream (glycerol-3-phosphate acyltransferases; GPAT) or downstream (diacylglycerol acyltransferases; DGAT) of the diacylglycerol step. Although both inhibitions reduced LD formation in cardiomyocytes treated with FA and LD inducers, only DGAT inhibition impaired metabolic stress-stimulated glucose uptake. DGAT inhibition in FA plus TPA-treated cardiomyocytes reduced triacylglycerol but not diacylglycerol content, thus increasing the diacylglycerol/triacylglycerol ratio. In cardiomyocytes exposed to FA alone, GPAT inhibition reduced diacylglycerol but not triacylglycerol, thus decreasing the diacylglycerol/triacylglycerol ratio, prevented PKCδ activation and improved metabolic stress-stimulated glucose uptake. Changes in AMP-activated Protein Kinase activity failed to explain variations in metabolic stress-stimulated glucose uptake. Thus, LD formation regulates metabolic stress-stimulated glucose uptake in a manner best reflected by the diacylglycerol/triacylglycerol ratio.
在应对缺血代谢应激时,刺激葡萄糖摄取对于心肌细胞的功能和存活非常重要。慢性暴露于脂肪酸 (FA) 会损害葡萄糖摄取的刺激作用,而脂滴 (LD) 的诱导与保留葡萄糖摄取有关。然而,LD 诱导防止葡萄糖摄取受损的机制仍不清楚。我们用十四烷酰佛波醇乙酸酯 (TPA) 或 5-氨基咪唑-4-羧酰胺-1-β-D-核糖呋喃苷 (AICAR) 诱导 LD。在 FA + LD 诱导剂暴露的心肌细胞中,甘油-3-磷酸酰基转移酶 (GPAT) 或二酰基甘油酰基转移酶 (DGAT) 上下游的三酰甘油生物合成酶被抑制。尽管这两种抑制作用都减少了 FA 和 LD 诱导剂处理的心肌细胞中的 LD 形成,但只有 DGAT 抑制会损害代谢应激刺激的葡萄糖摄取。FA + TPA 处理的心肌细胞中 DGAT 的抑制作用降低了三酰甘油但没有降低二酰基甘油的含量,从而增加了二酰基甘油/三酰甘油的比例。在单独暴露于 FA 的心肌细胞中,GPAT 抑制降低了二酰基甘油但没有降低三酰甘油,从而降低了二酰基甘油/三酰甘油的比例,阻止了 PKCδ 的激活并改善了代谢应激刺激的葡萄糖摄取。AMP 激活蛋白激酶活性的变化无法解释代谢应激刺激的葡萄糖摄取的变化。因此,LD 的形成以最好地反映二酰基甘油/三酰甘油比例的方式调节代谢应激刺激的葡萄糖摄取。