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Myelin-Associated Glycoprotein and Its Axonal Receptors
被引:121
作者:
Schnaar, Ronald L.
[1
,2
]
Lopez, Pablo H. H.
[1
]
机构:
[1] Johns Hopkins Sch Med, Dept Pharmacol, Baltimore, MD 21205 USA
[2] Johns Hopkins Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
基金:
美国国家卫生研究院;
关键词:
MAG;
gangliosides;
GD1a;
GT1b;
Nogo;
NgR;
axon regeneration;
LACKING COMPLEX GANGLIOSIDES;
NEURITE OUTGROWTH INHIBITION;
SPINAL-CORD-INJURY;
ACID BINDING-SITE;
I-TYPE LECTINS;
NOGO-66;
RECEPTOR;
NERVOUS-SYSTEM;
MICE DEFICIENT;
FUNCTIONAL RECOVERY;
ADHESION MOLECULES;
D O I:
10.1002/jnr.21992
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Myelin-associated glycoprotein (MAG) is expressed on the innermost myelin membrane wrap, directly apposed to the axon surface. Although it is not required for myelination, MAG enhances long-term axon-myelin stability, helps to structure nodes of Ranvier, and regulates the axon cytoskeleton. In addition to its role in axon-myelin stabilization, MAG inhibits axon regeneration after injury; MAG and a discrete set of other molecules on residual myelin membranes at injury sites actively signal axons to halt elongation. Both the stabilizing and the axon outgrowth inhibitory effects of MAG are mediated by complementary MAG receptors on the axon surface. Two MAG receptor families have been described, sialoglycans (specifically gangliosides GD1a and GT1b) and Nogo receptors (NgRs). Controversies remain about which receptor(s) mediates which of MAG's biological effects. Here we review the findings and challenges in associating MAG's biological effects with specific receptors. (C) 2009 Wiley-Liss, Inc.
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页码:3267 / 3276
页数:10
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