Cargando…

IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers

Tetanic electrical stimulation induces two separate calcium signals in rat skeletal myotubes, a fast one, dependent on Cav 1.1 or dihydropyridine receptors (DHPRs) and ryanodine receptors and related to contraction, and a slow signal, dependent on DHPR and inositol trisphosphate receptors (IP(3)Rs)...

Descripción completa

Detalles Bibliográficos
Autores principales: Casas, Mariana, Figueroa, Reinaldo, Jorquera, Gonzalo, Escobar, Matías, Molgó, Jordi, Jaimovich, Enrique
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2947059/
https://www.ncbi.nlm.nih.gov/pubmed/20837675
http://dx.doi.org/10.1085/jgp.200910397
_version_ 1782187360624050176
author Casas, Mariana
Figueroa, Reinaldo
Jorquera, Gonzalo
Escobar, Matías
Molgó, Jordi
Jaimovich, Enrique
author_facet Casas, Mariana
Figueroa, Reinaldo
Jorquera, Gonzalo
Escobar, Matías
Molgó, Jordi
Jaimovich, Enrique
author_sort Casas, Mariana
collection PubMed
description Tetanic electrical stimulation induces two separate calcium signals in rat skeletal myotubes, a fast one, dependent on Cav 1.1 or dihydropyridine receptors (DHPRs) and ryanodine receptors and related to contraction, and a slow signal, dependent on DHPR and inositol trisphosphate receptors (IP(3)Rs) and related to transcriptional events. We searched for slow calcium signals in adult muscle fibers using isolated adult flexor digitorum brevis fibers from 5–7-wk-old mice, loaded with fluo-3. When stimulated with trains of 0.3-ms pulses at various frequencies, cells responded with a fast calcium signal associated with muscle contraction, followed by a slower signal similar to one previously described in cultured myotubes. Nifedipine inhibited the slow signal more effectively than the fast one, suggesting a role for DHPR in its onset. The IP(3)R inhibitors Xestospongin B or C (5 µM) also inhibited it. The amplitude of post-tetanic calcium transients depends on both tetanus frequency and duration, having a maximum at 10–20 Hz. At this stimulation frequency, an increase of the slow isoform of troponin I mRNA was detected, while the fast isoform of this gene was inhibited. All three IP(3)R isoforms were present in adult muscle. IP(3)R-1 was differentially expressed in different types of muscle fibers, being higher in a subset of fast-type fibers. Interestingly, isolated fibers from the slow soleus muscle did not reveal the slow calcium signal induced by electrical stimulus. These results support the idea that IP(3)R-dependent slow calcium signals may be characteristic of distinct types of muscle fibers and may participate in the activation of specific transcriptional programs of slow and fast phenotype.
format Text
id pubmed-2947059
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-29470592011-04-01 IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers Casas, Mariana Figueroa, Reinaldo Jorquera, Gonzalo Escobar, Matías Molgó, Jordi Jaimovich, Enrique J Gen Physiol Article Tetanic electrical stimulation induces two separate calcium signals in rat skeletal myotubes, a fast one, dependent on Cav 1.1 or dihydropyridine receptors (DHPRs) and ryanodine receptors and related to contraction, and a slow signal, dependent on DHPR and inositol trisphosphate receptors (IP(3)Rs) and related to transcriptional events. We searched for slow calcium signals in adult muscle fibers using isolated adult flexor digitorum brevis fibers from 5–7-wk-old mice, loaded with fluo-3. When stimulated with trains of 0.3-ms pulses at various frequencies, cells responded with a fast calcium signal associated with muscle contraction, followed by a slower signal similar to one previously described in cultured myotubes. Nifedipine inhibited the slow signal more effectively than the fast one, suggesting a role for DHPR in its onset. The IP(3)R inhibitors Xestospongin B or C (5 µM) also inhibited it. The amplitude of post-tetanic calcium transients depends on both tetanus frequency and duration, having a maximum at 10–20 Hz. At this stimulation frequency, an increase of the slow isoform of troponin I mRNA was detected, while the fast isoform of this gene was inhibited. All three IP(3)R isoforms were present in adult muscle. IP(3)R-1 was differentially expressed in different types of muscle fibers, being higher in a subset of fast-type fibers. Interestingly, isolated fibers from the slow soleus muscle did not reveal the slow calcium signal induced by electrical stimulus. These results support the idea that IP(3)R-dependent slow calcium signals may be characteristic of distinct types of muscle fibers and may participate in the activation of specific transcriptional programs of slow and fast phenotype. The Rockefeller University Press 2010-10 /pmc/articles/PMC2947059/ /pubmed/20837675 http://dx.doi.org/10.1085/jgp.200910397 Text en © 2010 Casas 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 Article
Casas, Mariana
Figueroa, Reinaldo
Jorquera, Gonzalo
Escobar, Matías
Molgó, Jordi
Jaimovich, Enrique
IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers
title IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers
title_full IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers
title_fullStr IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers
title_full_unstemmed IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers
title_short IP(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers
title_sort ip(3)-dependent, post-tetanic calcium transients induced by electrostimulation of adult skeletal muscle fibers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2947059/
https://www.ncbi.nlm.nih.gov/pubmed/20837675
http://dx.doi.org/10.1085/jgp.200910397
work_keys_str_mv AT casasmariana ip3dependentposttetaniccalciumtransientsinducedbyelectrostimulationofadultskeletalmusclefibers
AT figueroareinaldo ip3dependentposttetaniccalciumtransientsinducedbyelectrostimulationofadultskeletalmusclefibers
AT jorqueragonzalo ip3dependentposttetaniccalciumtransientsinducedbyelectrostimulationofadultskeletalmusclefibers
AT escobarmatias ip3dependentposttetaniccalciumtransientsinducedbyelectrostimulationofadultskeletalmusclefibers
AT molgojordi ip3dependentposttetaniccalciumtransientsinducedbyelectrostimulationofadultskeletalmusclefibers
AT jaimovichenrique ip3dependentposttetaniccalciumtransientsinducedbyelectrostimulationofadultskeletalmusclefibers