Literature DB >> 10942887

Reciprocal interactions between perisynaptic Schwann cells and regenerating nerve terminals at the frog neuromuscular junction.

S Koirala1, H Qiang, C P Ko.   

Abstract

The perisynaptic Schwann cell (PSC) has gained recent attention with respect to its roles in synaptic function, remodeling, and regeneration at the vertebrate neuromuscular junction (NMJ). Here we test the hypothesis that, following nerve injury, processes extended by PSCs guide regenerating nerve terminals (NTs) in vivo, and that the extension of sprouts by PSCs is triggered by the arrival of regenerating NTs. Frog NMJs were double-stained with a fluorescent dye, FM4-64, for NTs, and fluorescein isothiocyanate (FITC)-tagged peanut agglutinin (PNA) for PSCs. Identified NMJs were imaged in vivo repeatedly for several months after nerve injury. PSCs sprouted profusely beginning 3-4 weeks after nerve transection and, as reinnervation progressed, regenerating NTs closely followed the preceding PSC sprouts, which could extend tens to hundreds of microns beyond the original synaptic site. The pattern of reinnervation was dictated by PSC sprouts, which could form novel routes joining neighboring junctions or develop into new myelinated axonal pathways. In contrast to mammals, profuse PSC sprouting in frog muscles was not seen in response to axotomy alone, and did not occur at chronically denervated NMJs. Instead, sprouting coincided with the arrival of regenerating NTs. Immunofluorescent staining revealed that in muscle undergoing reinnervation 4 weeks after axotomy, 91% of NMJs bore PSC sprouts, compared to only 6% of NMJs in muscle that was chronically denervated for 4 weeks. These results suggest that reciprocal interactions between regenerating NTs and PSCs govern the process of reinnervation at frog NMJs: regenerating NTs induce PSCs to sprout, and PSC sprouts, in turn, lead and guide the elaboration of NTs. Copyright 2000 John Wiley & Sons, Inc.

Entities:  

Mesh:

Year:  2000        PMID: 10942887     DOI: 10.1002/1097-4695(20000905)44:3<343::aid-neu5>3.0.co;2-o

Source DB:  PubMed          Journal:  J Neurobiol        ISSN: 0022-3034


  12 in total

1.  Schwann cells express active agrin and enhance aggregation of acetylcholine receptors on muscle fibers.

Authors:  J F Yang; G Cao; S Koirala; L V Reddy; C P Ko
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

2.  Synapse-glia interactions at the mammalian neuromuscular junction.

Authors:  D Rochon; I Rousse; R Robitaille
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

Review 3.  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

4.  Schwann cell-derived factors modulate synaptic activities at developing neuromuscular synapses.

Authors:  Guan Cao; Chien-Ping Ko
Journal:  J Neurosci       Date:  2007-06-20       Impact factor: 6.167

5.  Terminal Schwann cells participate in neuromuscular synapse remodeling during reinnervation following nerve injury.

Authors:  Hyuno Kang; Le Tian; Michelle Mikesh; Jeff W Lichtman; Wesley J Thompson
Journal:  J Neurosci       Date:  2014-04-30       Impact factor: 6.167

6.  Presynaptic secretion of mind-the-gap organizes the synaptic extracellular matrix-integrin interface and postsynaptic environments.

Authors:  Emma Rushton; Jeffrey Rohrbough; Kendal Broadie
Journal:  Dev Dyn       Date:  2009-03       Impact factor: 3.780

7.  Distinct muscarinic acetylcholine receptor subtypes contribute to stability and growth, but not compensatory plasticity, of neuromuscular synapses.

Authors:  Megan C Wright; Srilatha Potluri; Xueyong Wang; Eva Dentcheva; Dinesh Gautam; Alan Tessler; Jürgen Wess; Mark M Rich; Young-Jin Son
Journal:  J Neurosci       Date:  2009-11-25       Impact factor: 6.167

8.  Macrophage-Derived Vascular Endothelial Growth Factor-A Is Integral to Neuromuscular Junction Reinnervation after Nerve Injury.

Authors:  Chuieng-Yi Lu; Katherine B Santosa; Albina Jablonka-Shariff; Bianca Vannucci; Anja Fuchs; Isaiah Turnbull; Deng Pan; Matthew D Wood; Alison K Snyder-Warwick
Journal:  J Neurosci       Date:  2020-11-06       Impact factor: 6.167

9.  Ciliary neurotrophic factor is not required for terminal sprouting and compensatory reinnervation of neuromuscular synapses: re-evaluation of CNTF null mice.

Authors:  Megan C Wright; Young-Jin Son
Journal:  Exp Neurol       Date:  2007-03-21       Impact factor: 5.330

10.  Axonal regeneration after sciatic nerve lesion is delayed but complete in GFAP- and vimentin-deficient mice.

Authors:  Alexander Berg; Johan Zelano; Marcela Pekna; Ulrika Wilhelmsson; Milos Pekny; Staffan Cullheim
Journal:  PLoS One       Date:  2013-11-01       Impact factor: 3.240

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