Marcus Jill, Popko Brian
UNC Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, USA.
Biochim Biophys Acta. 2002 Dec 19;1573(3):406-13. doi: 10.1016/s0304-4165(02)00410-5.
Myelination is a developmentally regulated process whereby myelinating glial cells elaborate large quantities of a specialized plasma membrane that ensheaths axons. The myelin sheath contains an unusual lipid composition in that the glycolipid galactosylceramide (GalC) and its sulfated form sulfatide constitute a large proportion of the total lipid mass. These glycolipids have been implicated in a range of developmental processes such as cell differentiation and myelination initiation, but analyses of mice lacking UDP-galactose:ceramide galactosyltransferase (CGT), the enzyme required for myelin galactolipid synthesis, have more recently demonstrated that the galactolipids more subtly regulate myelin formation. The CGT mutants display a delay in myelin maturation and axo-glial interactions develop abnormally. By interbreeding the CGT mutants with mice that lack myelin-associated glycoprotein, it has been shown that these specialized myelin lipids and proteins act in concert to promote axo-glial adhesion during myelinogenesis. The analysis of the CGT mutants is helping to clarify the roles myelin galactolipids play in regulating the development, and ultimately the function of the myelin sheath.
髓鞘形成是一个受发育调控的过程,在此过程中,形成髓鞘的神经胶质细胞会精心合成大量包裹轴突的特殊质膜。髓鞘含有一种不同寻常的脂质成分,其中糖脂半乳糖基神经酰胺(GalC)及其硫酸化形式硫苷脂占总脂质质量的很大一部分。这些糖脂参与了一系列发育过程,如细胞分化和髓鞘形成起始,但最近对缺乏UDP-半乳糖:神经酰胺半乳糖基转移酶(CGT)(髓鞘半乳糖脂合成所需的酶)的小鼠的分析表明,半乳糖脂对髓鞘形成的调节更为精细。CGT突变体在髓鞘成熟方面表现出延迟,轴突与神经胶质细胞的相互作用也出现异常。通过将CGT突变体与缺乏髓鞘相关糖蛋白的小鼠杂交,已表明这些特殊的髓鞘脂质和蛋白质在髓鞘形成过程中协同作用,促进轴突与神经胶质细胞的黏附。对CGT突变体的分析有助于阐明髓鞘半乳糖脂在调节髓鞘发育以及最终髓鞘功能方面所起的作用。