Poulos A
Department of Chemical Pathology, Women's and Children's Hospital, North Adelaide, South Australia.
Lipids. 1995 Jan;30(1):1-14. doi: 10.1007/BF02537036.
Fatty acids with greater than 22 carbon atoms (very long chain fatty acids, VLCFA) are present in small amounts in most animal tissues. Saturated and monoenoic VLCFA are major components of brain, while the polyenoic VLCFA occur in significant amounts in certain specialized animal tissues such as retina and spermatozoa. Biosynthesis of VLCFA occurs by carbon chain elongation of shorter chain fatty acid precursors while beta-oxidation takes place almost exclusively in peroxisomes. Mitochondria are unable to oxidize VLCFA because they lack a specific VLCFA coenzyme A synthetase, the first enzyme in the beta-oxidation pathway. VLCFA accumulate in the tissues of patients with inherited abnormalities in peroxisomal assembly, and also in individuals with defects in enzymes catalyzing individual reactions along the beta-oxidation pathway. It is believed that the accumulation of VLCFA in patient tissues contributes to the severe pathological changes which are a feature of these conditions. However, little is known of the role of VLCFA in normal cellular processes, and of the molecular basis for their contribution to the disease process. The present review provides an outline of the current knowledge of VLCFA including their biosynthesis, degradation, possible function and involvement in human disease.
碳原子数超过22个的脂肪酸(极长链脂肪酸,VLCFA)在大多数动物组织中含量很少。饱和及单烯极长链脂肪酸是大脑的主要成分,而多烯极长链脂肪酸在某些特殊动物组织如视网膜和精子中大量存在。极长链脂肪酸的生物合成是通过较短链脂肪酸前体的碳链延长进行的,而β-氧化几乎只在过氧化物酶体中发生。线粒体无法氧化极长链脂肪酸,因为它们缺乏一种特定的极长链脂肪酸辅酶A合成酶,即β-氧化途径中的第一种酶。极长链脂肪酸会在过氧化物酶体组装存在遗传性异常的患者组织中蓄积,也会在沿β-氧化途径催化个别反应的酶存在缺陷的个体组织中蓄积。据信,极长链脂肪酸在患者组织中的蓄积会导致严重的病理变化,而这些变化是这些病症的一个特征。然而,人们对极长链脂肪酸在正常细胞过程中的作用以及它们导致疾病过程的分子基础知之甚少。本综述概述了目前关于极长链脂肪酸的知识,包括它们的生物合成、降解、可能的功能以及与人类疾病的关系。