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Long-term live cell microscopy studies of lipid droplet fusion dynamics in adipocytes

机译:脂肪细胞中脂滴融合动力学的长期活细胞显微镜研究

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摘要

During the adipogenic differentiation process of mesenchymal stem cells, lipid droplets (LDs) grow slowly by transferring lipids between each other. Recent findings hint at the possibility that a fusion pore is involved. In this study, we analyze lipid transfer data obtained in long-term label-free microscopy studies in the framework of a Hagen-Poiseuille model. The data obtained show a LD fusion process in which the lipid transfer directionality depends on the size difference between LDs, whereas the respective rates depend on the size difference and additionally on the diameter of the smaller LDs. For the data analysis, the viscosity of the transferred material has to be known. We demonstrate that a viscosity-dependent molecular rotor dye can be used to measure LD viscosities in live cells. On this basis, we calculate the diameter of a putative lipid transfer channel which appears to have a direct dependence on the diameter of the smaller of the two participating LDs.
机译:在间充质干细胞的成脂分化过程中,脂质滴(LDs)通过彼此之间转移脂质而缓慢生长。最近的发现提示可能存在融合孔。在这项研究中,我们分析了在Hagen-Poiseuille模型的框架下在长期无标签显微镜研究中获得的脂质转移数据。所获得的数据显示了一种LD融合过程,其中脂质转移的方向性取决于LD之间的大小差异,而各自的比率取决于大小差异以及较小LD的直径。为了进行数据分析,必须知道被转移材料的粘度。我们证明,粘度依赖性分子转子染料可用于测量活细胞中的LD粘度。在此基础上,我们计算了一个假定的脂质转移通道的直径,该通道似乎直接取决于两个参与的LD中较小者的直径。

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