Literature DB >> 10673559

Recycling and refilling of transmitter quanta at the frog neuromuscular junction.

W Van der Kloot1, C Colasante, R Cameron, J Molgó.   

Abstract

1. Fluorescent dyes have been used at the frog neuromuscular junction to label synaptic vesicular membrane. Retrieved membrane is reformed into vesicles, which are released along with pre-existing vesicles. Consequently, if vesicular refilling with acetylcholine (ACh) is depressed by inhibitors, two sizes of quanta should be released: normal and smaller. As recycling continues the fraction of smaller size quanta should increase exponentially. 2. We enhanced the rate of quantal release by elevating the K+ concentration. The principal inhibitors were (-)-vesamicol (VES), hemicholinium-3 (HC3), and NH4+. Quantal size measurements were fitted to one and to two cumulative lognormal probability distribution functions. When two fitted better, the statistical significance assessment took into account the three additional parameters used in calculating the fit. 3. After recycling in the presence of inhibitor, many sets were fitted better by two lognormal functions. As recycling continued, the fraction of the miniature endplate potential voltage-time integrals ( MEPPs) in the larger sub-population decreased exponentially. 4. The size of the releasable pool was estimated by counting the quanta released by carbonyl cyanide m-chlorophenylhydrazone (CCCP). This was compared to pool sizes calculated from the inhibitor experiments. The two estimates of pool size were indistinguishable, with mean values ranging from about 170,000 to 270,000. 5. With all of the treatments tested, the means of the sizes in the smaller sub-population of MEPPs were about 1/3 those of the larger sub-populations. 6. Recycling synaptic vesicles appear to be incorporated into the releasable pool from which they have roughly the same probability of release as the pre-existing vesicles.

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Year:  2000        PMID: 10673559      PMCID: PMC2269784          DOI: 10.1111/j.1469-7793.2000.00247.x

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


  39 in total

1.  Synaptic vesicle dynamics in rat fast and slow motor nerve terminals.

Authors:  B Reid; C R Slater; G S Bewick
Journal:  J Neurosci       Date:  1999-04-01       Impact factor: 6.167

2.  PRESYNAPTIC ACTION OF HEMICHOLINIUM AT THE NEUROMUSCULAR JUNCTION.

Authors:  D ELMQVIST; D M QUASTEL
Journal:  J Physiol       Date:  1965-04       Impact factor: 5.182

3.  Role of mitochondrial dysfunction in the Ca2+-induced decline of transmitter release at K+-depolarized motor neuron terminals.

Authors:  M A Calupca; G M Hendricks; J C Hardwick; R L Parsons
Journal:  J Neurophysiol       Date:  1999-02       Impact factor: 2.714

Review 4.  The synaptic vesicle cycle.

Authors:  W J Betz; J K Angleson
Journal:  Annu Rev Physiol       Date:  1998       Impact factor: 19.318

Review 5.  How does a vesicle know it is full?

Authors:  J Williams
Journal:  Neuron       Date:  1997-05       Impact factor: 17.173

6.  Expression of a putative vesicular acetylcholine transporter facilitates quantal transmitter packaging.

Authors:  H Song; G Ming; E Fon; E Bellocchio; R H Edwards; M Poo
Journal:  Neuron       Date:  1997-05       Impact factor: 17.173

7.  The effects of nerve stimulation and hemicholinium on synaptic vesicles at the mammalian euromuscular junction.

Authors:  S F Jones; S Kwanbunbumpen
Journal:  J Physiol       Date:  1970-03       Impact factor: 5.182

8.  Evidence that mitochondria buffer physiological Ca2+ loads in lizard motor nerve terminals.

Authors:  G David; J N Barrett; E F Barrett
Journal:  J Physiol       Date:  1998-05-15       Impact factor: 5.182

9.  Synaptic vesicle size and number are regulated by a clathrin adaptor protein required for endocytosis.

Authors:  B Zhang; Y H Koh; R B Beckstead; V Budnik; B Ganetzky; H J Bellen
Journal:  Neuron       Date:  1998-12       Impact factor: 17.173

10.  Kinetic parameters for the vesicular acetylcholine transporter: two protons are exchanged for one acetylcholine.

Authors:  M L Nguyen; G D Cox; S M Parsons
Journal:  Biochemistry       Date:  1998-09-22       Impact factor: 3.162

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5.  Repetitive nerve stimulation decreases the acetylcholine content of quanta at the frog neuromuscular junction.

Authors:  L A Naves; W Van der Kloot
Journal:  J Physiol       Date:  2001-05-01       Impact factor: 5.182

6.  Regulation of vesicular acetylcholine transporter by the activation of excitatory amino acid receptors in the avian retina.

Authors:  Nelson Enrique Loureiro-dos-Santos; Marco Antonio M Prado; Ricardo Augusto de Melo Reis; Patrícia F Gardino; Maria Christina F de Mello; Fernando G de Mello
Journal:  Cell Mol Neurobiol       Date:  2002-12       Impact factor: 5.046

7.  Vesicle size and transmitter release at the frog neuromuscular junction when quantal acetylcholine content is increased or decreased.

Authors:  William Van der Kloot; Jordi Molgó; Roger Cameron; Cesare Colasante
Journal:  J Physiol       Date:  2002-06-01       Impact factor: 5.182

8.  Presynaptic function is altered in snake K+-depolarized motor nerve terminals containing compromised mitochondria.

Authors:  M A Calupca; C Prior; L A Merriam; G M Hendricks; R L Parsons
Journal:  J Physiol       Date:  2001-04-01       Impact factor: 5.182

  8 in total

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