Werner Hauke B, Kuhlmann Katja, Shen Siming, Uecker Marina, Schardt Anke, Dimova Kalina, Orfaniotou Foteini, Dhaunchak Ajit, Brinkmann Bastian G, Möbius Wiebke, Guarente Lenny, Casaccia-Bonnefil Patrizia, Jahn Olaf, Nave Klaus-Armin
Department of Neurogenetics, Max Planck Institute of Experimental Medicine, D-37075 Goettingen, Germany.
J Neurosci. 2007 Jul 18;27(29):7717-30. doi: 10.1523/JNEUROSCI.1254-07.2007.
Mice lacking the expression of proteolipid protein (PLP)/DM20 in oligodendrocytes provide a genuine model for spastic paraplegia (SPG-2). Their axons are well myelinated but exhibit impaired axonal transport and progressive degeneration, which is difficult to attribute to the absence of a single myelin protein. We hypothesized that secondary molecular changes in PLP(null) myelin contribute to the loss of PLP/DM20-dependent neuroprotection and provide more insight into glia-axonal interactions in this disease model. By gel-based proteome analysis, we identified >160 proteins in purified myelin membranes, which allowed us to systematically monitor the CNS myelin proteome of adult PLP(null) mice, before the onset of disease. We identified three proteins of the septin family to be reduced in abundance, but the nicotinamide adenine dinucleotide (NAD+)-dependent deacetylase sirtuin 2 (SIRT2) was virtually absent. SIRT2 is expressed throughout the oligodendrocyte lineage, and immunoelectron microscopy revealed its association with myelin. Loss of SIRT2 in PLP(null) was posttranscriptional, suggesting that PLP/DM20 is required for its transport into the myelin compartment. Because normal SIRT2 activity is controlled by the NAD+/NADH ratio, its function may be coupled to the axo-glial metabolism and the long-term support of axons by oligodendrocytes.
少突胶质细胞中缺乏蛋白脂蛋白(PLP)/DM20表达的小鼠为痉挛性截瘫(SPG-2)提供了一个真实模型。它们的轴突有良好的髓鞘形成,但轴突运输受损且进行性退化,这很难归因于单一髓鞘蛋白的缺失。我们推测,PLP基因敲除小鼠髓鞘中的继发性分子变化导致了PLP/DM20依赖性神经保护作用的丧失,并为该疾病模型中的胶质细胞-轴突相互作用提供了更多见解。通过基于凝胶的蛋白质组分析,我们在纯化的髓鞘膜中鉴定出>160种蛋白质,这使我们能够在疾病发作前系统地监测成年PLP基因敲除小鼠的中枢神经系统髓鞘蛋白质组。我们发现septin家族的三种蛋白质丰度降低,但烟酰胺腺嘌呤二核苷酸(NAD+)依赖性脱乙酰酶沉默调节蛋白2(SIRT2)几乎不存在。SIRT2在整个少突胶质细胞谱系中表达,免疫电子显微镜显示其与髓鞘相关。PLP基因敲除小鼠中SIRT2的缺失是转录后水平的,这表明PLP/DM20是其转运到髓鞘区室所必需的。由于正常的SIRT2活性受NAD+/NADH比率控制,其功能可能与轴突-胶质细胞代谢以及少突胶质细胞对轴突的长期支持有关。