Semaphorin 3A displays a punctate distribution on the surface of neuronal cells and interacts with proteoglycans in the extracellular matrix

被引:119
作者
De Wit, J
De Winter, F
Klooster, J
Verhaagen, J
机构
[1] Netherlands Inst Brain Res, NL-1105 AZ Amsterdam, Netherlands
[2] Netherlands Ophthalm Res Inst, NL-1005 BA Amsterdam, Netherlands
关键词
D O I
10.1016/j.mcn.2004.12.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Secreted semapborins are essential for neural development and continue to be expressed in subpopulations of adult neurons, where they subserve as yet unknown functions. We employed functional myc-and GFP-tagged Sema3A proteins to obtain insight in the localization of Sema3A in neuronal cells. Sema3A localized to both axons and dendrites of cortical neurons. GFP-Sema3A exhibited a characteristic punctate distribution on the surface of Neuro-2a cells, localized to migratory pathways of cultured cells, and co-localized with and induced clustering of its receptor component neuropilin-1. Treatment with excess glycosaminoglycans and chondroitinase ABC resulted in the removal of cell surface Sema3A. Heparin enhanced Sema3A's binding to neuropilin-1-expressing cells and potentiated its growth cone collapsing activity. Together, these results indicate that association with proteoglycans in the extracellular matrix of neuronal cells plays an important role in the localization of the chemorepulsive guidance cue Sema3A, and that this interaction may enhance its biological activity. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:40 / 55
页数:16
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