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FSP27 and PLIN1 interaction promotes the formation of large lipid droplets in human adipocytes.

机译:Fsp27和pLIN1相互作用促进人脂肪细胞中大脂滴的形成。

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摘要

Human adipocytes express high levels of two distinct lipid droplet proteins, fat specific protein 27 (FSP27; also called CIDEC), a member of the CIDE family, and perilipin1 (PLIN1), a member of the PAT family. Both proteins play a role in fat metabolism in adipocytes, but how they interact is not known. Our present study demonstrates that FSP27 and PLIN1 co-localize and interact in cultured human primary adipocytes. We also found that the C-terminal domain of FSP27, aa 120-220, interacts with PLIN1. Individual expression of exogenous FSP27 or PLIN1 increased triglyceride content and decreased glycerol release (a measure of lipolysis), but co-expression of both proteins did not further increase triglyceride content or decrease lipolysis in human adipocytes. However, the combination of PLIN1 and FSP27 increased the average size of lipid droplets or caused the formation of unilocular adipocytes. Our data suggest that FSP27 interacts with PLIN1 to regulate lipid droplet size in human adipocytes in a concerted manner.
机译:人脂肪细胞高水平表达两种不同的脂滴蛋白,即CIDE家族成员的脂肪特异性蛋白27(FSP27;也称为CIDEC)和PAT家族成员periplipin1(PLIN1)。两种蛋白都在脂肪细胞中的脂肪代谢中起作用,但如何相互作用尚不清楚。我们目前的研究表明,FSP27和PLIN1在培养的人原代脂肪细胞中共定位并相互作用。我们还发现FSP27的C末端结构域氨基酸120-220与PLIN1相互作用。外源性FSP27或PLIN1的单独表达增加了甘油三酸酯的含量,并降低了甘油的释放(一种脂解作用),但是两种蛋白的共表达并没有进一步增加人脂肪细胞中的甘油三酯含量或降低脂解作用。但是,PLIN1和FSP27的组合增加了脂滴的平均大小,或导致了单眼脂肪细胞的形成。我们的数据表明FSP27与PLIN1相互作用,以协调的方式调节人脂肪细胞中的脂滴大小。

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