Literature DB >> 6279825

Electrophysiological and freeze-fracture studies of changes following denervation at frog neuromuscular junctions.

C P Ko.   

Abstract

1. Changes which occur at frog neuromuscular junctions following denervation have been studied by combining intracellular recording and freeze-fracture electron microscopy. 2. Shortly after nerve section, both neuromuscular transmission and intramembrane structures of neuromuscular junctions remain normal. 3. Later, neuromuscular transmission fails, beginning with the disappearance of end-plate potentials (e.p.p.s) and followed by the disappearance of miniature end-plate potentials (m.e.p.p.s). The frequency of m.e.p.p.s which persist after cessation of e.p.p.s is not increased dramatically in K+-rich or hypertonic solutions. 4. Concomitant with the changes of transmission are changes in intramembrane structures. The first sign of these changes in disruption of active zones, which become disorganized, fragmented or vanish. Nerve terminals then disintegrate and eventually are engulfed by Schwann cells. 5. When neuromuscular transmission has failed completely, former sites of the neuromuscular junction are occupied by Schwann cells. These cells develop transverse ridges which lie opposed to junctional folds, just like active zones of nerve terminals. However, the ridges on Schwann cells do not contain organized rows of particles or clusters of any synaptic organelles, even at later stages when Schwann cell m.e.p.p.s commence. 6. It is suggested that the failure of e.p.p.s involves at least an impairment of the transmitter release mechanism at the nerve terminal, which is probably associated with the disruption of active zones. The cessation of m.e.p.p.s is thought to be caused by the engulfment of terminals by Schwann cells.

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Year:  1981        PMID: 6279825      PMCID: PMC1249649          DOI: 10.1113/jphysiol.1981.sp014007

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  34 in total

1.  The effect of calcium-ionophores on acetylcholine release from Schwann cells.

Authors:  Y Ito; R Miledi
Journal:  Proc R Soc Lond B Biol Sci       Date:  1977-02-11

2.  Properties of spontaneous potentials at denervated motor endplates of the frog.

Authors:  S Bevan; W Grampp; R Miledi
Journal:  Proc R Soc Lond B Biol Sci       Date:  1976-10-15

3.  Ultrastructural studies of normal and degenerating mouse neuromuscular junctions.

Authors:  W Winlow; P N Usherwood
Journal:  J Neurocytol       Date:  1975-08

4.  Electrophysiological studies of normal and degenerating mouse neuromuscular junctions.

Authors:  W Winlow; P N Usherwood
Journal:  Brain Res       Date:  1976-07-16       Impact factor: 3.252

5.  Structure and ultrastructure of the frog motor endplate. A freeze-etching study.

Authors:  K Peper; F Dreyer; C Sandri; K Akert; H Moor
Journal:  Cell Tissue Res       Date:  1974-06-24       Impact factor: 5.249

6.  Non-transmitting neuromuscular junctions during an early stage of end-plate reinnervation.

Authors:  M J Dennis; R Miledi
Journal:  J Physiol       Date:  1974-06       Impact factor: 5.182

7.  Initial changes in the neuromuscular synapses of denervated rat diaphragm.

Authors:  S Manolov
Journal:  Brain Res       Date:  1974-01-11       Impact factor: 3.252

8.  Ultrastructure of the "active zone" in the frog neuromuscular junction.

Authors:  F Dreyer; K Peper; K Akert; C Sandri; H Moor
Journal:  Brain Res       Date:  1973-11-23       Impact factor: 3.252

9.  Electrically induced release of acetylcholine from denervated Schwann cells.

Authors:  M J Dennis; R Miledi
Journal:  J Physiol       Date:  1974-03       Impact factor: 5.182

10.  Release of transmitter from degenerating locust motorneurones.

Authors:  P N Usherwood
Journal:  J Exp Biol       Date:  1973-08       Impact factor: 3.312

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  10 in total

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

Authors:  G T Macleod; P A Dickens; M R Bennett
Journal:  J Neurosci       Date:  2001-04-01       Impact factor: 6.167

2.  Transmitter secretion in the frog neuromuscular synapse after prolonged exposure to calcium-free solutions.

Authors:  A L Zefirov; R D Mukhamedzyanov; M G Minlebaev; S Yu Cheranov; M M Abdrakhmanov; P N Grigor'ev
Journal:  Neurosci Behav Physiol       Date:  2003-07

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.  Precision of reinnervation and synaptic remodeling observed in neuromuscular junctions of living frogs.

Authors:  S H Astrow; V Pitaevski; A A Herrera
Journal:  J Neurosci       Date:  1996-08-15       Impact factor: 6.167

5.  Profiles of evoked release along the length of frog motor nerve terminals.

Authors:  A J D'Alonzo; A D Grinnell
Journal:  J Physiol       Date:  1985-02       Impact factor: 5.182

6.  A sex difference in synaptic efficacy at the laryngeal neuromuscular junction of Xenopus laevis.

Authors:  M L Tobias; D B Kelley; M Ellisman
Journal:  J Neurosci       Date:  1995-03       Impact factor: 6.167

7.  Acetylcholine release at identified nerve terminals in the organ-cultured frog neuromuscular preparation.

Authors:  R Cherki-Vakil; H Meiri
Journal:  J Physiol       Date:  1990-04       Impact factor: 5.182

8.  Active zones on motor nerve terminals contain alpha 3beta 1 integrin.

Authors:  M W Cohen; B G Hoffstrom; D W DeSimone
Journal:  J Neurosci       Date:  2000-07-01       Impact factor: 6.167

9.  Characteristics of Schwann-cell miniature end-plate currents in denervated frog muscle.

Authors:  G Reiser; R Miledi
Journal:  Pflugers Arch       Date:  1988-07       Impact factor: 3.657

10.  Regeneration of the active zone at the frog neuromuscular junction.

Authors:  C P Ko
Journal:  J Cell Biol       Date:  1984-05       Impact factor: 10.539

  10 in total

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