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Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80–100-Hz calls lasting ∼500 ms interleaved with silent periods (intercall interv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003191/ https://www.ncbi.nlm.nih.gov/pubmed/24733838 http://dx.doi.org/10.1085/jgp.201411160 |
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author | Nelson, Frank E. Hollingworth, Stephen Rome, Lawrence C. Baylor, Stephen M. |
author_facet | Nelson, Frank E. Hollingworth, Stephen Rome, Lawrence C. Baylor, Stephen M. |
author_sort | Nelson, Frank E. |
collection | PubMed |
description | The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80–100-Hz calls lasting ∼500 ms interleaved with silent periods (intercall intervals) lasting ∼10 s. To understand the intracellular movements of Ca(2+) during the intercall intervals, superfast fibers were microinjected with fluo-4, a high-affinity fluorescent Ca(2+) indicator, and stimulated by trains of 40 action potentials at 83 Hz, which mimics fiber activity during calling. The fluo-4 fluorescence signal was measured during and after the stimulus trains; the signal was also simulated with a kinetic model of the underlying myoplasmic Ca(2+) movements, including the binding and transport of Ca(2+) by the sarcoplasmic reticulum (SR) Ca(2+) pumps. The estimated total amount of Ca(2+) released from the SR during a first stimulus train is ∼6.5 mM (concentration referred to the myoplasmic water volume). At 40 ms after cessation of stimulation, the myoplasmic free Ca(2+) concentration ([Ca(2+)]) is below the threshold for force generation (∼3 µM), yet the estimated concentration of released Ca(2+) remaining in the myoplasm (Δ[Ca(M)]) is large, ∼5 mM, with ∼80% bound to parvalbumin. At 10 s after stimulation, [Ca(2+)] is ∼90 nM (three times the assumed resting level) and Δ[Ca(M)] is ∼1.3 mM, with 97% bound to parvalbumin. Ca(2+) movements during the intercall interval thus appear to be strongly influenced by (a) the accumulation of Ca(2+) on parvalbumin and (b) the slow rate of Ca(2+) pumping that ensues when parvalbumin lowers [Ca(2+)] near the resting level. With repetitive stimulus trains initiated at 10-s intervals, Ca(2+) release and pumping come quickly into balance as a result of the stability (negative feedback) supplied by the increased rate of Ca(2+) pumping at higher [Ca(2+)]. |
format | Online Article Text |
id | pubmed-4003191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40031912014-11-01 Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder Nelson, Frank E. Hollingworth, Stephen Rome, Lawrence C. Baylor, Stephen M. J Gen Physiol Research Articles The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80–100-Hz calls lasting ∼500 ms interleaved with silent periods (intercall intervals) lasting ∼10 s. To understand the intracellular movements of Ca(2+) during the intercall intervals, superfast fibers were microinjected with fluo-4, a high-affinity fluorescent Ca(2+) indicator, and stimulated by trains of 40 action potentials at 83 Hz, which mimics fiber activity during calling. The fluo-4 fluorescence signal was measured during and after the stimulus trains; the signal was also simulated with a kinetic model of the underlying myoplasmic Ca(2+) movements, including the binding and transport of Ca(2+) by the sarcoplasmic reticulum (SR) Ca(2+) pumps. The estimated total amount of Ca(2+) released from the SR during a first stimulus train is ∼6.5 mM (concentration referred to the myoplasmic water volume). At 40 ms after cessation of stimulation, the myoplasmic free Ca(2+) concentration ([Ca(2+)]) is below the threshold for force generation (∼3 µM), yet the estimated concentration of released Ca(2+) remaining in the myoplasm (Δ[Ca(M)]) is large, ∼5 mM, with ∼80% bound to parvalbumin. At 10 s after stimulation, [Ca(2+)] is ∼90 nM (three times the assumed resting level) and Δ[Ca(M)] is ∼1.3 mM, with 97% bound to parvalbumin. Ca(2+) movements during the intercall interval thus appear to be strongly influenced by (a) the accumulation of Ca(2+) on parvalbumin and (b) the slow rate of Ca(2+) pumping that ensues when parvalbumin lowers [Ca(2+)] near the resting level. With repetitive stimulus trains initiated at 10-s intervals, Ca(2+) release and pumping come quickly into balance as a result of the stability (negative feedback) supplied by the increased rate of Ca(2+) pumping at higher [Ca(2+)]. The Rockefeller University Press 2014-05 /pmc/articles/PMC4003191/ /pubmed/24733838 http://dx.doi.org/10.1085/jgp.201411160 Text en © 2014 Nelson et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Nelson, Frank E. Hollingworth, Stephen Rome, Lawrence C. Baylor, Stephen M. Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder |
title | Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder |
title_full | Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder |
title_fullStr | Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder |
title_full_unstemmed | Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder |
title_short | Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder |
title_sort | intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003191/ https://www.ncbi.nlm.nih.gov/pubmed/24733838 http://dx.doi.org/10.1085/jgp.201411160 |
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