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A dynamic, cytoplasmic triacylglycerol pool in enterocytes revealed by ex vivo and in vivo coherent anti-Stokes Raman scattering imagings⃞

机译:通过离体和体内相干抗斯托克斯拉曼散射成像揭示肠道细胞中动态的胞浆三酰基甘油池

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摘要

The absorptive cells of the small intestine, enterocytes, are not generally thought of as a cell type that stores triacylglycerols (TGs) in cytoplasmic lipid droplets (LDs). We revisit TG metabolism in enterocytes by ex vivo and in vivo coherent anti-Stokes Raman scattering (CARS) imaging of small intestine of mice during dietary fat absorption (DFA). We directly visualized the presence of LDs in enterocytes. We determined lipid amount and quantified LD number and size as a function of intestinal location and time post-lipid challenge via gavage feeding. The LDs were confirmed to be primarily TG by biochemical analysis. Combined CARS and fluorescence imaging indicated that the large LDs were located in the cytoplasm, associated with the tail-interacting protein of 47 kDa. Furthermore, in vivo CARS imaging showed real-time variation in the amount of TG stored in LDs through the process of DFA. Our results highlight a dynamic, cytoplasmic TG pool in enterocytes that may play previously unexpected roles in processes, such as regulating postprandial blood TG concentrations.
机译:小肠的吸收性细胞,肠上皮细胞,通常不被认为是在细胞质脂质滴(LDs)中存储三酰甘油(TGs)的细胞类型。我们通过离体和饮食脂肪吸收(DFA)期间小鼠小肠的体内相干抗斯托克斯拉曼散射(CARS)成像来重新研究肠细胞中的TG代谢。我们直接观察了肠上皮细胞中LD的存在。我们通过管饲喂养确定了脂质的量,并确定了LD的数量和大小与肠道位置和脂质激发后时间的关系。通过生化分析确认LDs主要是TG。结合CARS和荧光成像表明,大的LD位于细胞质中,与47 kDa的尾部相互作用蛋白有关。此外,体内CARS成像显示通过DFA处理,LD中存储的TG量实时变化。我们的结果强调了肠上皮细胞中动态的细胞质TG池,该池可能在过程中发挥了以前未曾预料到的作用,例如调节餐后血液TG的浓度。

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