Simons Mikael, Kramer Eva-Maria, Macchi Paolo, Rathke-Hartlieb Silvia, Trotter Jacqueline, Nave Klaus-Armin, Schulz Jorg B
Department of Neurology, University of Tübingen, 72076 Tübingen, Germany.
J Cell Biol. 2002 Apr 15;157(2):327-36. doi: 10.1083/jcb.200110138.
Duplications and overexpression of the proteolipid protein (PLP) gene are known to cause the dysmyelinating disorder Pelizaeus-Merzbacher disease (PMD). To understand the cellular response to overexpressed PLP in PMD, we have overexpressed PLP in BHK cells and primary cultures of oligodendrocytes with the Semliki Forest virus expression system. Overexpressed PLP was routed to late endosomes/lysosomes and caused a sequestration of cholesterol in these compartments. Similar results were seen in transgenic mice overexpressing PLP. With time, the endosomal/lysosomal accumulation of cholesterol and PLP led to an increase in the amount of detergent-insoluble cellular cholesterol and PLP. In addition, two fluorescent sphingolipids, BODIPY-lactosylceramide and -galactosylceramide, which under normal conditions are sorted to the Golgi apparatus, were missorted to perinuclear structures. This was also the case for the lipid raft marker glucosylphosphatidylinositol-yellow fluorescence protein, which under normal steady-state conditions is localized on the plasma membrane and to the Golgi complex. Taken together, we show that overexpression of PLP leads to the formation of endosomal/lysosomal accumulations of cholesterol and PLP, accompanied by the mistrafficking of raft components. We propose that these accumulations perturb the process of myelination and impair the viability of oligodendrocytes.
已知蛋白脂质蛋白(PLP)基因的重复和过表达会导致脱髓鞘疾病佩利措伊斯-梅茨巴赫病(PMD)。为了解PMD中细胞对过表达的PLP的反应,我们利用辛德毕斯病毒表达系统在BHK细胞和少突胶质细胞原代培养物中过表达了PLP。过表达的PLP被转运至晚期内体/溶酶体,并导致这些区室中胆固醇的隔离。在过表达PLP的转基因小鼠中也观察到了类似结果。随着时间的推移,胆固醇和PLP在内体/溶酶体中的积累导致细胞中去污剂不溶性胆固醇和PLP的量增加。此外,两种荧光鞘脂,硼二吡咯乳糖神经酰胺和半乳糖神经酰胺,在正常情况下会被分选至高尔基体,却被错误分选至核周结构。脂质筏标记物糖基磷脂酰肌醇-黄色荧光蛋白也是如此,在正常稳态条件下它定位于质膜和高尔基体复合体。综上所述,我们表明PLP的过表达导致胆固醇和PLP在内体/溶酶体中积累的形成,同时伴有筏成分的错误运输。我们认为这些积累扰乱了髓鞘形成过程并损害了少突胶质细胞的活力。