生物化学
脂肪酸
酰基辅酶A
新陈代谢
脂肪酸代谢
生物
酰基转移酶
酶
脂质代谢
功能(生物学)
基因亚型
代谢途径
细胞生物学
基因
作者
Douglas G. Mashek,Lei O. Li,Rosalind Coleman
出处
期刊:Future Lipidology
[Future Medicine]
日期:2007-08-01
卷期号:2 (4): 465-476
被引量:230
标识
DOI:10.2217/17460875.2.4.465
摘要
AbstractAbstractThirteen 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. Furthermore, 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, fatty acid 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.Key words: Acyl-Coaβ-OxidationFatty AcidGlycerolipidPhospholipidTriacylglycerol
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