脂蛋白脂酶
分解代谢
化学
脂质代谢
生物化学
脂蛋白
极低密度脂蛋白
生物
胆固醇
脂肪酶
新陈代谢
脂解
乳糜微粒
酶
脂肪组织
标识
DOI:10.1097/mol.0000000000000297
摘要
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.
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