Chang Benny Hung-Junn, Li Lan, Paul Antoni, Taniguchi Susumu, Nannegari Vijayalakshmi, Heird William C, Chan Lawrence
Division of Diabetes, Endocrinology, and Metabolism, Departments of Medicine and Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
Mol Cell Biol. 2006 Feb;26(3):1063-76. doi: 10.1128/MCB.26.3.1063-1076.2006.
Adipose differentiation-related protein (ADFP; also known as ADRP or adipophilin), is a lipid droplet (LD) protein found in most cells and tissues. ADFP expression is strongly induced in cells with increased lipid load. We have inactivated the Adfp gene in mice to better understand its role in lipid accumulation. The Adfp-deficient mice have unaltered adipose differentiation or lipolysis in vitro or in vivo. Importantly, they display a 60% reduction in hepatic triglyceride (TG) and are resistant to diet-induced fatty liver. To determine the mechanism for the reduced hepatic TG content, we measured hepatic lipogenesis, very-low-density lipoprotein (VLDL) secretion, and lipid uptake and utilization, all of which parameters were shown to be similar between mutant and wild-type mice. The finding of similar VLDL output in the presence of a reduction in total TG in the Adfp-deficient liver is explained by the retention of TG in the microsomes where VLDL is assembled. Given that lipid droplets are thought to form from the outer leaflet of the microsomal membrane, the reduction of TG in the cytosol with concomitant accumulation of TG in the microsome of Adfp-/- cells suggests that ADFP may facilitate the formation of new LDs. In the absence of ADFP, impairment of LD formation is associated with the accumulation of microsomal TG but a reduction in TG in other subcellular compartments.
脂肪分化相关蛋白(ADFP;也称为ADRP或脂联素)是一种在大多数细胞和组织中发现的脂滴(LD)蛋白。在脂质负荷增加的细胞中,ADFP表达被强烈诱导。我们已经使小鼠中的Adfp基因失活,以更好地了解其在脂质积累中的作用。Adfp基因缺陷型小鼠在体外或体内的脂肪分化或脂解没有改变。重要的是,它们的肝脏甘油三酯(TG)减少了60%,并且对饮食诱导的脂肪肝具有抗性。为了确定肝脏TG含量降低的机制,我们测量了肝脏脂肪生成、极低密度脂蛋白(VLDL)分泌以及脂质摄取和利用,结果显示突变型和野生型小鼠之间所有这些参数都相似。在Adfp基因缺陷型肝脏中总TG减少的情况下,VLDL输出相似这一发现可以通过TG保留在组装VLDL的微粒体中来解释。鉴于脂滴被认为是由微粒体膜的外小叶形成的,Adfp基因敲除细胞的细胞质中TG减少,同时微粒体中TG积累,这表明ADFP可能促进新脂滴的形成。在没有ADFP的情况下,脂滴形成的受损与微粒体TG的积累有关,但其他亚细胞区室中的TG减少。