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OSBP-related protein 2 is a sterol receptor on lipid droplets that regulates the metabolism of neutral lipids

机译:OSBP相关蛋白2是脂质小滴上的固醇受体调节中性脂质的代谢

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摘要

Oxysterol binding protein-related protein 2 (ORP2) is a member of the oxysterol binding protein family, previously shown to bind 25-hydroxycholesterol and implicated in cellular cholesterol metabolism. We show here that ORP2 also binds 22(R)-hydroxycholesterol [22(R)OHC], 7-ketocholesterol, and cholesterol, with 22(R)OHC being the highest affinity ligand of ORP2 (Kd 1.4 × 10−8 M). We report the localization of ORP2 on cytoplasmic lipid droplets (LDs) and its function in neutral lipid metabolism using the human A431 cell line as a model. The ORP2 LD association depends on sterol binding: Treatment with 5 μM 22(R)OHC inhibits the LD association, while a mutant defective in sterol binding is constitutively LD bound. Silencing of ORP2 using RNA interference slows down cellular triglyceride hydrolysis. Furthermore, ORP2 silencing increases the amount of [14C]cholesteryl esters but only under conditions in which lipogenesis and LD formation are enhanced by treatment with oleic acid. The results identify ORP2 as a sterol receptor present on LD and provide evidence for its role in the regulation of neutral lipid metabolism, possibly as a factor that integrates the cellular metabolism of triglycerides with that of cholesterol.
机译:氧固醇结合蛋白相关蛋白2(ORP2)是氧固醇结合蛋白家族的成员,以前被证明与25-羟基胆固醇结合并参与细胞胆固醇代谢。我们在这里显示,ORP2还结合22(R)-羟基胆固醇[22(R)OHC],7-酮胆固醇和胆固醇,其中22(R)OHC是ORP2的最高亲和力配体(Kd 1.4×10s- 8 M)。我们报告ORP2在细胞质脂质滴(LDs)上的定位及其在使用人A431细胞系作为模型的中性脂质代谢中的功能。 ORP2 LD缔合依赖于固醇结合:用5μM22(R)OHC处理可抑制LD缔合,而固醇结合缺陷的突变型则组成性地与LD结合。使用RNA干扰沉默ORP2会减慢细胞甘油三酸酯的水解。此外,ORP2沉默可增加[ 14 C]胆固醇酯的含量,但仅在通过油酸处理提高脂肪生成和LD形成的条件下。结果确定ORP2是LD上存在的一种固醇受体,并提供了其在中性脂质代谢调节中的作用的证据,可能是将甘油三酸酯与胆固醇的细胞代谢整合在一起的一个因素。

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