Literature DB >> 10766919

Action potential waveform voltage clamp shows significance of different Ca2+ channel types in developing ascidian muscle.

J E Dallman1, J B Dorman, W J Moody.   

Abstract

1. Early in development, ascidian muscle cells generate spontaneous, long-duration action potentials that are mediated by a high-threshold, inactivating Ca2+ current. This spontaneous activity is required for appropriate physiological development. 2. Mature muscle cells generate brief action potentials only in response to motor neuron input. The mature action potential is mediated by a high-threshold sustained Ca2+ current. 3. Action potentials recorded from these two stages were imposed as voltage-clamp commands on cells of the same and different stages from which they were recorded. This strategy allowed us to study how immature and mature Ca2+ currents are optimized to their particular functions. 4. Total Ca2+ entry during an action potential did not change during development. The developmental increase in Ca2+ current density exactly compensated for decreased spike duration. This compensation was a function purely of Ca2+ current density, not of the transition from immature to mature Ca2+ current types. 5. In immature cells, Ca2+ entry was spread out over the entire waveform of spontaneous activity, including the interspike voltage trajectory. This almost continuous Ca2+ entry may be important in triggering Ca2+-dependent developmental programmes, and is a function of the slightly more negative voltage dependence of the immature Ca2+ current. 6. In contrast, Ca2+ entry in mature cells was confined to the action potential itself, because of the slightly more positive voltage dependence of the mature Ca2+ current. This may be important in permitting rapid contraction-relaxation cycles during larval swimming. 7. The inactivation of the immature Ca2+ current serves to limit the frequency and burst duration of spontaneous activity. The sustained kinetics of the mature Ca2+ current permit high-frequency firing during larval swimming.

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Year:  2000        PMID: 10766919      PMCID: PMC2269877          DOI: 10.1111/j.1469-7793.2000.t01-1-00375.x

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


  16 in total

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Authors:  R S Scroggs; A P Fox
Journal:  J Neurosci       Date:  1992-05       Impact factor: 6.167

2.  Reopening of Ca2+ channels in mouse cerebellar neurons at resting membrane potentials during recovery from inactivation.

Authors:  P A Slesinger; J B Lansman
Journal:  Neuron       Date:  1991-11       Impact factor: 17.173

Review 3.  A developmental handshake: neuronal control of ionic currents and their control of neuronal differentiation.

Authors:  N C Spitzer
Journal:  J Neurobiol       Date:  1991-10

4.  Action potential waveform voltage-clamp commands reveal striking differences in calcium entry via low and high voltage-activated calcium channels.

Authors:  D P McCobb; K G Beam
Journal:  Neuron       Date:  1991-07       Impact factor: 17.173

5.  Time course of Ca and Ca-dependent K currents during molluscan nerve cell action potentials.

Authors:  M Gola; N Hussy; M Crest; C Ducreux
Journal:  Neurosci Lett       Date:  1986-10-20       Impact factor: 3.046

Review 6.  Critical periods of early development created by the coordinate modulation of ion channel properties.

Authors:  W J Moody
Journal:  Perspect Dev Neurobiol       Date:  1995

Review 7.  Control of spontaneous activity during development.

Authors:  W J Moody
Journal:  J Neurobiol       Date:  1998-10

8.  Comparison of ionic currents expressed in immature and mature muscle cells of an ascidian larva.

Authors:  A K Davis; A A Greaves; J E Dallman; W J Moody
Journal:  J Neurosci       Date:  1995-07       Impact factor: 6.167

9.  Transmission by presynaptic spike-like depolarization in the squid giant synapse.

Authors:  R Llinás; M Sugimori; S M Simon
Journal:  Proc Natl Acad Sci U S A       Date:  1982-04       Impact factor: 11.205

10.  Muscarinic activation of ionic currents measured by a new whole-cell recording method.

Authors:  R Horn; A Marty
Journal:  J Gen Physiol       Date:  1988-08       Impact factor: 4.086

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  5 in total

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3.  The self-regulating nature of spontaneous synchronized activity in developing mouse cortical neurones.

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Journal:  J Physiol       Date:  2006-08-31       Impact factor: 5.182

4.  Opposing effects of spinal nerve ligation on calcium-activated potassium currents in axotomized and adjacent mammalian primary afferent neurons.

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Journal:  Brain Res       Date:  2006-12-20       Impact factor: 3.252

5.  Cellular properties of intrinsically photosensitive retinal ganglion cells during postnatal development.

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Journal:  Neural Dev       Date:  2019-08-30       Impact factor: 3.842

  5 in total

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