Regulatory Mechanisms of Nervous Systems with Glycosphingolipids

被引:37
作者
Furukawa, Koichi [1 ]
Ohmi, Yuhsuke [1 ]
Ohkawa, Yuki [1 ]
Tokuda, Noriyo [1 ]
Kondo, Yuji [1 ]
Tajima, Orie [2 ]
Furukawa, Keiko [2 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Biochem 2, Showa Ku, Nagoya, Aichi 4660065, Japan
[2] Chubu Univ, Coll Life & Hlth Sci, Dept Life & Med Sci, Aichi 4878501, Japan
关键词
Gangliosides; Inflammation; Degeneration; Rafts; Complement; Knockout; COMPLEX GANGLIOSIDES; LIPID RAFTS; MICE; GM3; INFLAMMATION; DISEASE; NEURODEGENERATION; DEGENERATION; REGENERATION; MICRODOMAINS;
D O I
10.1007/s11064-011-0494-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A number of studies have suggested functions of sialic acid-containing glycosphingolipids (gangliosides) in the nervous system. However, results of analyses of the mutant mice lacking gangliosides suggested that they play crucial roles in the maintenance of integrity and repair of the nervous tissues. Furthermore, results of double knockout mice lacking all gangliosides except GM3 (GM3-only mice) suggested that deficiency of gangliosides induced complement activation and inflammation, leading to neurodegeneration. Generation of triple knockout mice by mating GM3-only mice and C3-deficient mice verified the involvement of complement systems in the inflammation and neurodegeneration. For the mechanisms of the complement activation, functional disorders of complement-regulatory proteins such as CD55 and CD59, which belong to GPI-anchored proteins, should be main factors. These results suggested that normal composition of gangliosides is essential for the maintenance of lipid rafts. Therefore, it was suggested that regulation of the complement systems and suppression of the inflammation should be important for the treatment of neurodegeneration, having common aspects with other neurodegenerative diseases such as Alzheimer disease.
引用
收藏
页码:1578 / 1586
页数:9
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