Stowers Institute for Medical Research, Kansas City, MO 64110, USA.
Proc Natl Acad Sci U S A. 2010 Mar 9;107(10):4640-5. doi: 10.1073/pnas.0912308107. Epub 2010 Feb 22.
Dietary fat accumulates in lipid droplets or endolysosomal compartments that undergo selective expansion under normal or pathophysiological conditions. We find that genetic defects in a peroxisomal beta-oxidation pathway cause size expansion in lipid droplets that are distinct from the lysosome-related organelles in Caenorhabditis elegans. Expansion of lipid droplets is accompanied by an increase in triglycerides (TAG) that are resistant to fasting- or TAG lipase-triggered lipolysis. Nevertheless, in mutant animals, a diet poor in vaccenic acid reduced the TAG level and lipid droplet size. Our results implicate peroxisomal dysfunction in pathologic lipid droplet expansion in animals and illustrate how dietary factors modulate the phenotype of such genetic defects.
膳食脂肪积累在脂滴或内溶酶体隔室中,在正常或病理生理条件下这些隔室会发生选择性扩张。我们发现,过氧化物酶体β-氧化途径中的遗传缺陷会导致线虫中与溶酶体相关的细胞器不同的脂滴大小扩张。脂滴的扩张伴随着甘油三酯(TAG)的增加,而这种 TAG 对禁食或 TAG 脂肪酶触发的脂肪分解有抗性。然而,在突变动物中,缺乏葵酸的饮食会降低 TAG 水平和脂滴大小。我们的结果表明,过氧化物酶体功能障碍与动物病理性脂滴扩张有关,并说明了饮食因素如何调节这种遗传缺陷的表型。