Radom J, Salvayre R, Mussini J M, De Lisle B, Negre A, Maret A, Billaudel S, Douste-Blazy L
Laboratorie de Biochimie, INSERM 101, Faculté de Médecine Toulouse-Purpan, France.
Biol Cell. 1988;62(1):39-45.
A new variant of multisystemic lipid storage myopathy (type 3) has been identified. Human cultured fibroblasts present a major triacylglycerol storage whereas other neutral lipids and phospholipids are in the normal range. When feeding the cells in the presence of radiolabelled oleic acid we observed an accumulation of radiolabelled triacylglycerols demonstrating the endogenous biosynthesis of the stored triacylglycerols. After a 72-hr chase period, no degradation of radiolabelled triacylglycerols was observed. Histochemical examination of multisystemic lipid storage myopathy skin fibroblasts showed a massive accumulation of neutral lipids (stained by the fluorescent probe Nile Red) in cells grown in medium supplemented with 10% fetal calf serum. These cytoplasmic vacuoles were not obviously membrane-surrounded as shown by electron microscopy.
已鉴定出一种多系统脂质贮积性肌病(3型)的新变体。人类培养的成纤维细胞存在大量三酰甘油储存,而其他中性脂质和磷脂处于正常范围。当在放射性标记油酸存在的情况下培养细胞时,我们观察到放射性标记的三酰甘油积累,这表明储存的三酰甘油是内源性生物合成的。在72小时的追踪期后,未观察到放射性标记的三酰甘油降解。对多系统脂质贮积性肌病皮肤成纤维细胞的组织化学检查显示,在补充有10%胎牛血清的培养基中生长的细胞中,中性脂质(由荧光探针尼罗红染色)大量积累。如电子显微镜所示,这些细胞质空泡没有明显的膜包围。