Literature DB >> 9634561

Axon withdrawal during synapse elimination at the neuromuscular junction is accompanied by disassembly of the postsynaptic specialization and withdrawal of Schwann cell processes.

S M Culican1, C C Nelson, J W Lichtman.   

Abstract

Nerve terminal withdrawal is accompanied by a loss of acetylcholine receptors (AChRs) at corresponding postsynaptic sites during the process of synapse elimination at developing () and reinnervated adult () neuromuscular junctions. Aside from AChR and nerve terminal loss, however, the molecular and cellular alterations that occur at sites of elimination are unknown. To gain a better understanding of the cascade of events that leads to the disassembly of synaptic sites during the synapse elimination process, we surveyed the distribution of molecular elements of the postsynaptic specialization, the basal lamina, and supporting Schwann cells during the process of synapse elimination that occurs after reinnervation. In addition, quantitative techniques were used to determine the temporal order of disappearance of molecules that were lost relative to the loss of postsynaptic AChRs. We found that the dismantling of the postsynaptic specialization was inhomogeneous, with evidence of rapid dissolution of some aspects of the postsynaptic apparatus and slower loss of others. We also observed a loss of Schwann cell processes from sites of synapse elimination, with a time course similar to that seen for nerve terminal retraction. In contrast, all of the extracellular markers that we examined were lost slowly from sites of synapse loss. We therefore conclude that the synapse elimination process is synapse-wide, removing not only nerve terminals but also Schwann cells and many aspects of the postsynaptic apparatus. The disassembly occurs in a stereotyped sequence with some synaptic elements appearing much more stable than others.

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Year:  1998        PMID: 9634561      PMCID: PMC6792572     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  45 in total

1.  Complex end-plate potentials at the regenerating neuromuscular junction of the rat.

Authors:  J J McArdle
Journal:  Exp Neurol       Date:  1975-12       Impact factor: 5.330

2.  ACh receptor-rich membrane domains organized in fibroblasts by recombinant 43-kildalton protein.

Authors:  W D Phillips; C Kopta; P Blount; P D Gardner; J H Steinbach; J P Merlie
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3.  The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo.

Authors:  T M DeChiara; D C Bowen; D M Valenzuela; M V Simmons; W T Poueymirou; S Thomas; E Kinetz; D L Compton; E Rojas; J S Park; C Smith; P S DiStefano; D J Glass; S J Burden; G D Yancopoulos
Journal:  Cell       Date:  1996-05-17       Impact factor: 41.582

4.  Nerve terminal withdrawal from rat neuromuscular junctions induced by neuregulin and Schwann cells.

Authors:  J T Trachtenberg; W J Thompson
Journal:  J Neurosci       Date:  1997-08-15       Impact factor: 6.167

5.  Alterations in synaptic strength preceding axon withdrawal.

Authors:  H Colman; J Nabekura; J W Lichtman
Journal:  Science       Date:  1997-01-17       Impact factor: 47.728

6.  Long-term synapse loss induced by focal blockade of postsynaptic receptors.

Authors:  R J Balice-Gordon; J W Lichtman
Journal:  Nature       Date:  1994-12-08       Impact factor: 49.962

7.  The postsynaptic 43K protein clusters muscle nicotinic acetylcholine receptors in Xenopus oocytes.

Authors:  S C Froehner; C W Luetje; P B Scotland; J Patrick
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8.  Neural cell adhesion molecule (N-CAM) accumulates in denervated and paralyzed skeletal muscles.

Authors:  J Covault; J R Sanes
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

9.  Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution.

Authors:  M E Adams; M H Butler; T M Dwyer; M F Peters; A A Murnane; S C Froehner
Journal:  Neuron       Date:  1993-09       Impact factor: 17.173

10.  A novel 87,000-Mr protein associated with acetylcholine receptors in Torpedo electric organ and vertebrate skeletal muscle.

Authors:  C Carr; G D Fischbach; J B Cohen
Journal:  J Cell Biol       Date:  1989-10       Impact factor: 10.539

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  16 in total

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Authors:  F Woodward Hopf; Jack Waters; Samar Mehta; Stephen J Smith
Journal:  J Neurosci       Date:  2002-02-01       Impact factor: 6.167

Review 2.  Perisynaptic Schwann Cells at the Neuromuscular Synapse: Adaptable, Multitasking Glial Cells.

Authors:  Chien-Ping Ko; Richard Robitaille
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-08-20       Impact factor: 10.005

3.  Rapid synapse elimination after postsynaptic protein synthesis inhibition in vivo.

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Journal:  J Neurosci       Date:  2007-05-30       Impact factor: 6.167

4.  Terminal Schwann cells participate in the competition underlying neuromuscular synapse elimination.

Authors:  Ian W Smith; Michelle Mikesh; Young il Lee; Wesley J Thompson
Journal:  J Neurosci       Date:  2013-11-06       Impact factor: 6.167

5.  Antibodies against low-density lipoprotein receptor-related protein 4 induce myasthenia gravis.

Authors:  Chengyong Shen; Yisheng Lu; Bin Zhang; Dwight Figueiredo; Jonathan Bean; Jiung Jung; Haitao Wu; Arnab Barik; Dong-Min Yin; Wen-Cheng Xiong; Lin Mei
Journal:  J Clin Invest       Date:  2013-11-08       Impact factor: 14.808

6.  Neuregulin1 displayed on motor axons regulates terminal Schwann cell-mediated synapse elimination at developing neuromuscular junctions.

Authors:  Young Il Lee; Yue Li; Michelle Mikesh; Ian Smith; Klaus-Armin Nave; Markus H Schwab; Wesley J Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  2016-01-11       Impact factor: 11.205

7.  The Agrin/MuSK signaling pathway is spatially segregated from the neuregulin/ErbB receptor signaling pathway at the neuromuscular junction.

Authors:  J C Trinidad; G D Fischbach; J B Cohen
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

8.  Primary afferent synapses on developing and adult Renshaw cells.

Authors:  George Z Mentis; Valerie C Siembab; Ricardo Zerda; Michael J O'Donovan; Francisco J Alvarez
Journal:  J Neurosci       Date:  2006-12-20       Impact factor: 6.167

9.  LRP4 is critical for neuromuscular junction maintenance.

Authors:  Arnab Barik; Yisheng Lu; Anupama Sathyamurthy; Andrew Bowman; Chengyong Shen; Lei Li; Wen-cheng Xiong; Lin Mei
Journal:  J Neurosci       Date:  2014-10-15       Impact factor: 6.167

10.  Axotomy or compression is required for axonal sprouting following end-to-side neurorrhaphy.

Authors:  Ayato Hayashi; Christopher Pannucci; Arash Moradzadeh; David Kawamura; Christina Magill; Daniel A Hunter; Alice Y Tong; Alexander Parsadanian; Susan E Mackinnon; Terence M Myckatyn
Journal:  Exp Neurol       Date:  2008-03-25       Impact factor: 5.330

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