The role of sphingolipids in neuronal development: Lessons from models of sphingolipid storage diseases

被引:25
作者
Buccoliero, R [1 ]
Bodennec, J [1 ]
Futerman, AH [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
基金
以色列科学基金会;
关键词
hippocampal neurons; ceramide; glucosylceramide; ganglioside; Gaucher disease; Sandhoff disease; Niemann-Pick disease;
D O I
10.1023/A:1020207613196
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
The study of sphingolipids has undergone a renaissance over the past decade due to the realization that these lipids are involved in a variety a biological processes, such as differentiation, apoptosis, cell growth, and cell migration. In the nervous system, sphingolipids, particularly gangliosides, have attracted particular attention as they occur at high levels and their levels change in a developmentally regulated program. Despite the fact that a large body of data has accumulated on the expression and metabolism of individual gangliosides within specific brain regions, the role of individual gangliosides in neuronal development is still poorly understood, and their specific functions are only now beginning to be elucidated. In the present article, we discuss various aspects of our current knowledge concerning the involvement of sphingolipids and gangliosides in neuronal development, and then discuss some recent findings that shed light on the role of sphingolipids and gangliosides obtained with animal models of sphingolipid and other lysosomal storage diseases.
引用
收藏
页码:565 / 574
页数:10
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