Cysteine-rich domain isoforms of the neuregulin-1 gene are required for maintenance of peripheral synapses

被引:248
作者
Wolpowitz, D
Mason, TBA
Dietrich, P
Mendelsohn, M
Talmage, DA
Role, LW
机构
[1] Columbia Univ Coll Phys & Surg, Program Neurobiol & Surg, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Neurol, New York, NY 10032 USA
[3] Columbia Univ Coll Phys & Surg, Dept Anat & Cell Biol, New York, NY 10032 USA
[4] Columbia Univ Coll Phys & Surg, Dept Genet & Dev, New York, NY 10032 USA
[5] Columbia Univ Coll Phys & Surg, Integrated Program Mol & Cellular Biol & Biophys, New York, NY 10032 USA
[6] Columbia Univ Coll Phys & Surg, Inst Human Nutr, New York, NY 10032 USA
[7] Columbia Univ Coll Phys & Surg, Dept Pediat, New York, NY 10032 USA
关键词
D O I
10.1016/S0896-6273(00)80873-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuregulin-1 (NRG-1) signaling has been implicated in inductive interactions between pre- and postsynaptic partners during synaptogenesis. We used gene targeting to selectively disrupt (c) under bar ysteine-(r) under bar ich (d) under bar omain(CRD-) containing NRG-1 isoforms. In CRD-NRG-1(-/-) mice, peripheral projections defasciculated and displayed aberrant branching patterns within their targets. Motor nerve terminals were transiently associated with broad bands of postsynaptic ACh receptor (AChR) clusters. Initially, Schwann cell precursors accompanied peripheral projections, but later, Schwann cells were absent from axons in the periphery. Following initial stages of synapse formation, sensory and motor nerves withdrew and degenerated. Our data demonstrate the essential role of CRD-NRG-1-mediated signaling for coordinating nerve, target, and Schwann cell interactions in the normal maintenance of peripheral synapses, and ultimately in the survival of CRD-NRG-1-expressing neurons.
引用
收藏
页码:79 / 91
页数:13
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