Jean Mayer US Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts, USA.
Nutr Rev. 2012 Oct;70(10):611-21. doi: 10.1111/j.1753-4887.2012.00515.x.
Perilipin proteins were discovered in the adipocyte, where they regulate lipid storage and lipolysis. Animal knockout models provided initial evidence of the critical role of perilipin 1, the most abundant of the adipocyte proteins, in energy and glucose metabolism. During a decade of study, genetic variation in perilipin 1 has been consistently but not invariably associated with body weight and obesity-related complications. Related phenotypes such as postprandial lipid metabolism and aerobic fitness are also modulated by perilipin 1 genotype, consistent with earlier metabolic studies. Investigations of gene-diet interactions, together with gene expression studies, have yielded increased understanding, but important questions about causal variants and mechanisms remain. The newest work examines perilipin 4, an adipocyte regulator of triglyceride synthesis and packaging. The novel discovery that a perilipin 4 variant creates a binding site for regulation of the perilipin gene (PLIN) by microRNA suggests intriguing new possibilities for additional mechanistic investigations of other perilipin proteins.
脂肪酶相关蛋白最初在脂肪细胞中被发现,其可以调节脂肪的储存和分解。动物敲除模型为脂肪酶相关蛋白 1(脂肪细胞中含量最丰富的蛋白)在能量和葡萄糖代谢中发挥关键作用提供了初步证据。在长达十年的研究中,脂肪酶相关蛋白 1 的遗传变异一直与体重和肥胖相关并发症相关,但并非始终如此。相关表型,如餐后脂质代谢和有氧健身,也受到脂肪酶相关蛋白 1 基因型的调节,这与早期的代谢研究一致。基因-饮食相互作用的研究,以及基因表达研究,增加了我们的认识,但关于因果变异和机制的重要问题仍然存在。最新的研究检查了脂肪酶相关蛋白 4,这是一种调节甘油三酯合成和包装的脂肪细胞调节剂。一个新的发现是,脂肪酶相关蛋白 4 的一个变异创造了一个结合位点,用于调节脂肪酶基因(PLIN)的微小 RNA,这为进一步研究其他脂肪酶相关蛋白的其他机制提供了有趣的新可能性。