Mashek Douglas G, Li Lei O, Coleman Rosalind A
Department of Food Science and Nutrition, University of Minnesota, St. Paul, Minnesota, 55108.
Future Lipidol. 2007 Aug;2(4):465-476. doi: 10.2217/17460875.2.4.465.
Thirteen homologous proteins comprise the long-chain acyl-CoA synthetase (ACSL), fatty acid transport protein (FATP), and bubblegum (ACSBG) subfamilies that activate long-chain and very-long-chain fatty acids to form acyl-CoAs. Gain- and loss-of-function studies show marked differences in the ability of these enzymes to channel fatty acids into different pathways of complex lipid synthesis. Further, the ability of the ACSLs and FATPs to enhance cellular FA uptake does not always require these proteins to be present on the plasma membrane; instead, FA uptake can be increased by enhancing its conversion to acyl-CoA and its metabolism in downstream pathways. Since altered fatty acid metabolism is a hallmark of numerous metabolic diseases and pathological conditions, the ACSL, FATP and ACSBG isoforms are likely to play important roles in disease etiology.
13种同源蛋白构成了长链酰基辅酶A合成酶(ACSL)、脂肪酸转运蛋白(FATP)和泡泡糖蛋白(ACSBG)亚家族,这些亚家族可激活长链和极长链脂肪酸以形成酰基辅酶A。功能获得和功能丧失研究表明,这些酶将脂肪酸导入复杂脂质合成不同途径的能力存在显著差异。此外,ACSL和FATP增强细胞脂肪酸摄取的能力并不总是要求这些蛋白存在于质膜上;相反,通过增强其转化为酰基辅酶A以及在下游途径中的代谢,脂肪酸摄取可以增加。由于脂肪酸代谢改变是众多代谢疾病和病理状况的一个标志,ACSL、FATP和ACSBG亚型可能在疾病病因学中发挥重要作用。