Literature DB >> 11264312

Formation and function of synapses with respect to Schwann cells at the end of motor nerve terminal branches on mature amphibian (Bufo marinus) muscle.

G T Macleod1, P A Dickens, M R Bennett.   

Abstract

A study has been made of the formation and regression of synapses with respect to Schwann cells at the ends of motor nerve terminal branches in mature toad (Bufo marinus) muscle. Synapse formation and regression, as inferred from the appearance and loss of N-(3-triethylammoniumpropyl)-4-(4-(dibutylamino)styryl) pyridinium dibromide (FM1-43)-stained vesicle clusters, occurred at the ends of terminal branches over a 16 hr period. Multiple microelectrodes placed in an array about FM1-43 blobs at the ends of terminal branches detected the electrical signs of neurotransmitter being released onto receptors. Injection of a calcium indicator (Oregon Green 488 BAPTA-1) into the motor nerve with subsequent imaging of the calcium transients, in response to stimulation, often showed a reduced calcium influx in the ends of terminal branches. Injection of a fluorescent dye into motor nerves revealed the full extent of their terminal branches and growing processes. Injection of the terminal Schwann cells (TSCs) often revealed pseudopodial TSC processes up to 10-microm-long. Imaging of these TSC processes over minutes or hours showed that they were highly labile and capable of extending several micrometers in a few minutes. Injection of motor nerve terminals with a different dye to that injected into their TSCs revealed that terminal processes sometimes followed the TSC processes over a few hours. It is suggested that the ends of motor nerve terminals in vivo are in a constant state of remodeling through the formation and regression of processes, that TSC processes guide the remodeling, and that it can occur over a relatively short period of time.

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Year:  2001        PMID: 11264312      PMCID: PMC6762398     

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


  54 in total

1.  Spatial variability in release at the frog neuromuscular junction measured with FM1-43.

Authors:  L G Wu; W J Betz
Journal:  Can J Physiol Pharmacol       Date:  1999-09       Impact factor: 2.273

2.  The probability of quantal secretion near a single calcium channel of an active zone.

Authors:  M R Bennett; L Farnell; W G Gibson
Journal:  Biophys J       Date:  2000-05       Impact factor: 4.033

3.  The formation of synapses in amphibian striated muscle during development.

Authors:  M R Bennett; A G Pettigrew
Journal:  J Physiol       Date:  1975-10       Impact factor: 5.182

4.  Dendritic spine changes associated with hippocampal long-term synaptic plasticity.

Authors:  F Engert; T Bonhoeffer
Journal:  Nature       Date:  1999-05-06       Impact factor: 49.962

5.  Synaptic remodeling revealed by repeated in vivo observations and electron microscopy of identified frog neuromuscular junctions.

Authors:  C P Ko; L Chen
Journal:  J Neurosci       Date:  1996-03-01       Impact factor: 6.167

6.  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

7.  Vesicle-associated proteins and calcium in nerve terminals of chick ciliary ganglia during development of facilitation.

Authors:  Y Q Lin; K L Brain; K A Nichol; J J Morgan; M R Bennett
Journal:  J Physiol       Date:  1996-12-15       Impact factor: 5.182

8.  Formation of the active zone at developing neuromuscular junctions in larval and adult bullfrogs.

Authors:  C P Ko
Journal:  J Neurocytol       Date:  1985-06

9.  Relationship between presynaptic calcium current and postsynaptic potential in squid giant synapse.

Authors:  R Llinás; I Z Steinberg; K Walton
Journal:  Biophys J       Date:  1981-03       Impact factor: 4.033

10.  Probabilistic secretion of quanta from nerve terminals in toad (Bufo marinus) muscle modulated by adenosine.

Authors:  M R Bennett; S Karunanithi; N A Lavidis
Journal:  J Physiol       Date:  1991-02       Impact factor: 5.182

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  6 in total

1.  Characteristics of calcium transient in different parts of frog nerve terminal in response to nerve impulse.

Authors:  D V Samigullin; A L Vasin; E A Bukharaeva; E E Nikolsky
Journal:  Dokl Biol Sci       Date:  2010 Mar-Apr

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

Review 3.  Clinical relevance of terminal Schwann cells: An overlooked component of the neuromuscular junction.

Authors:  Katherine B Santosa; Alexandra M Keane; Albina Jablonka-Shariff; Bianca Vannucci; Alison K Snyder-Warwick
Journal:  J Neurosci Res       Date:  2018-03-13       Impact factor: 4.164

4.  Purinergic junctional transmission and propagation of calcium waves in spinal cord astrocyte networks.

Authors:  Max R Bennett; Vlado Buljan; Les Farnell; William G Gibson
Journal:  Biophys J       Date:  2006-08-11       Impact factor: 4.033

5.  Glial imaging during synapse remodeling at the neuromuscular junction.

Authors:  Yi Zuo; Derron Bishop
Journal:  Neuron Glia Biol       Date:  2009-11-25

6.  T-box transcription factor 21 is expressed in terminal Schwann cells at the neuromuscular junction.

Authors:  Albina Jablonka-Shariff; Curtis Broberg; Rachel Rios; Alison K Snyder-Warwick
Journal:  Muscle Nerve       Date:  2021-05-12       Impact factor: 3.852

  6 in total

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