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神经节苷脂在脑组织中膜微区形成和维持中的基本作用。

Essential roles of gangliosides in the formation and maintenance of membrane microdomains in brain tissues.

机构信息

Department of Biochemistry II, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa-ku, Nagoya 466-0065, Japan.

出版信息

Neurochem Res. 2012 Jun;37(6):1185-91. doi: 10.1007/s11064-012-0764-7. Epub 2012 Apr 10.

DOI:10.1007/s11064-012-0764-7
PMID:22488331
Abstract

Gangliosides are considered to be involved in the maintenance and repair of nervous tissues. Recently, novel roles of gangliosides in the regulation of complement system were reported. Here we summarized roles of gangliosides in the formation and maintenance of membrane microdomains in brain tissues by comparing complement activation, inflammatory reaction and disruption of glycolipid-enriched microdomain (GEM)/rafts among several mutant mice of ganglioside synthases. Depending on the defects in ganglioside compositions, corresponding up-regulation of complement-related genes, proliferation of astrocytes and infiltration of microglia were found with gradual severity. Immunoblotting of fractions separated by sucrose density gradient ultracentrifugation revealed that DAF and NCAM having GPI-anchors tended to disappear from the raft fraction with intensities of DKO > GM2/GD2 synthase KO > GD3 synthase KO > WT. The lipid raft markers tended to disperse from the raft fractions with similar intensities. Phospholipids and cholesterol also tended to decrease in GEM/rafts in GM2/GD2 synthase KO and DKO, although total amounts were almost equivalent. All these results indicate that GEM/rafts architecture is destroyed by ganglioside deficiency with gradual intensity depending on the degree of defects of their compositions. Implication of inflammation caused by deficiency of gangliosides in various neurodegenerative diseases was discussed.

摘要

神经节苷脂被认为参与神经组织的维持和修复。最近,报道了神经节苷脂在补体系统调节中的新作用。在这里,我们通过比较几种神经节苷脂合成酶突变小鼠中补体激活、炎症反应和糖脂富集微区(GEM)/筏的破坏,总结了神经节苷脂在脑组织中膜微区形成和维持中的作用。根据神经节苷脂组成的缺陷,相应地发现补体相关基因的上调、星形胶质细胞的增殖和小胶质细胞的浸润逐渐加重。蔗糖密度梯度超速离心分离的级分的免疫印迹显示,具有 GPI 锚的 DAF 和 NCAM 倾向于从筏级分中消失,其强度为 DKO > GM2/GD2 合酶 KO > GD3 合酶 KO > WT。脂质筏标记物也倾向于以相似的强度从筏级分中分散。GM2/GD2 合酶 KO 和 DKO 中 GEM/筏的磷脂和胆固醇也倾向于减少,尽管总量几乎相等。所有这些结果表明,随着组成缺陷程度的增加,神经节苷脂缺乏会逐渐破坏 GEM/筏结构。讨论了神经节苷脂缺乏引起的各种神经退行性疾病中的炎症的影响。

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