Olivecrona Gunilla
Department of Medical Biosciences/Physiological Chemistry, Umeå University, Umeå, Sweden.
Curr Opin Lipidol. 2016 Jun;27(3):233-41. doi: 10.1097/MOL.0000000000000297.
A major step in energy metabolism is hydrolysis of triacylglycerol-rich lipoproteins (TRLs) to release fatty acids that can be used or stored. This is accomplished by lipoprotein lipase (LPL) at 'binding lipolysis sites' at the vascular endothelium. A multitude of interactions are involved in this seemingly simple reaction. Recent advances in the understanding of some of these factors will be discussed in an attempt to build a comprehensive picture.
The first event in catabolism of TRLs is that they dock at the vascular endothelium. This requires LPL and GPIHBP1, the endothelial transporter of LPL.Kinetic studies in rats with labeled chylomicrons showed that once a chylomicron has docked in the heart it stays for minutes and a large number of triacylglycerol molecules are split. The distribution of binding between tissues reflects the amount of LPL, as evident from studies with mutant mice.Clearance of TRLs is often slowed down in metabolic disease, as was demonstrated both in mice and men. In mice, this was directly connected to decreased amounts of endothelial LPL.
The LPL system is central in energy metabolism and results from interplay between several factors. Rapid and exciting progress is being made.
能量代谢的一个重要步骤是富含三酰甘油的脂蛋白(TRL)水解以释放可被利用或储存的脂肪酸。这是由脂蛋白脂肪酶(LPL)在血管内皮的“结合脂解位点”完成的。这个看似简单的反应涉及众多相互作用。本文将讨论对其中一些因素理解的最新进展,以期构建一个全面的图景。
TRL分解代谢的第一步是它们停靠在血管内皮。这需要LPL和LPL的内皮转运体GPIHBP1。对标记乳糜微粒的大鼠进行的动力学研究表明,一旦乳糜微粒停靠在心脏,它会停留数分钟,大量三酰甘油分子被分解。组织间结合的分布反映了LPL的量,这在对突变小鼠的研究中很明显。在代谢性疾病中,TRL的清除通常会减慢,这在小鼠和人类中都得到了证实。在小鼠中,这与内皮LPL量的减少直接相关。
LPL系统在能量代谢中起核心作用,是多种因素相互作用的结果。目前正在取得迅速而令人兴奋的进展。