Department of Ophthalmology, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9057, USA.
Br J Ophthalmol. 2010 Sep;94(9):1127-32. doi: 10.1136/bjo.2008.149286. Epub 2009 Aug 9.
Recent studies have established that retinal health depends on the presence of polyunsaturated C28-C36 fatty acids, in addition to docosahexaenoic acid (DHA, C22:6n-3). Initially characterised 20 years ago, these C28-C36 fatty acids are found as sn-1 acyl components of retinal phosphatidylcholines (PCs), which have DHA in the sn-2 position. This unique PC species is found in both rod- and cone-dominant retinas, mainly in the photoreceptor outer segments where the majority of phototransduction reactions take place. In bovine photoreceptor outer segments, this species is a significant component of lipid membranes. Its C28-C36 fatty acids account for 10 mol % of total PC fatty acids. Polyunsaturated C28-C36 fatty acids are synthesised in the retina, in contrast to eicosapentaenoic acid (EPA, C20:5n-3) and DHA which in humans are predominantly of dietary origin. Synthesis of C28-C36 fatty acids appears to be exclusively catalysed by elongase of very-long-chain fatty acids-4 (Elovl4). Mutations in Elovl4 cause Stargardt disease-3, a juvenile autosomal dominant macular degeneration. A mouse genetic model of the disease carries a human pathogenic 5 bp deletion in the mouse Elovl4 gene. It demonstrates early selective deficiency of retinal C28-C36 acyl PCs, followed later by reduced electroretinographic signals and increased accumulation of toxic N-retinylidene-N-retinylethanolamine (A2E).
近年来的研究表明,视网膜的健康不仅依赖于二十二碳六烯酸(DHA,C22:6n-3),还依赖于长链多不饱和 C28-C36 脂肪酸的存在。这些 C28-C36 脂肪酸最初是在 20 年前被确定的,它们是视网膜磷酯酰胆碱(PC)sn-1 酰基的组成部分,sn-2 位是 DHA。这种独特的 PC 物种存在于视杆细胞和视锥细胞占主导地位的视网膜中,主要存在于光感受器外段,大多数光转导反应都发生在那里。在牛的光感受器外段,这种物质是脂质膜的重要组成部分。其 C28-C36 脂肪酸占总 PC 脂肪酸的 10mol%。与二十碳五烯酸(EPA,C20:5n-3)和 DHA 不同,C28-C36 脂肪酸是在视网膜中合成的,而在人类中,这些脂肪酸主要来自饮食。C28-C36 脂肪酸的合成似乎是由长链脂肪酸延长酶 4(Elovl4)独家催化的。Elovl4 基因突变会导致 Stargardt 病-3,一种青少年常染色体显性黄斑变性。该疾病的小鼠遗传模型携带人类致病性的 5bp 缺失突变。它表现为视网膜 C28-C36 酰基 PC 的早期选择性缺乏,随后是视网膜电图信号降低和毒性 N-视黄醛-N-视黄醇乙胺(A2E)积累增加。