Am J Physiol Cell Physiol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 285: C56-C63, 2003. First published February 26, 2003; doi:10.1152/ajpcell.00377.2002
0363-6143/03 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
285/1/C56    most recent
00377.2002v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (39)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kubis, H.-P.
Right arrow Articles by Gros, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kubis, H.-P.
Right arrow Articles by Gros, G.

MUSCLE CELL BIOLOGY AND CELL MOTILITY

Ca2+ transients activate calcineurin/NFATc1 and initiate fast-to-slow transformation in a primary skeletal muscle culture

Hans-Peter Kubis, Nina Hanke, Renate J. Scheibe, Joachim D. Meissner, and Gerolf Gros

Zentrum Physiologie, Medizinische Hochschule Hannover, D-30625 Hannover, Germany

Submitted 20 August 2002 ; accepted in final form 11 February 2003

The calcineurin-mediated signal transduction via nuclear factor of activated T cells (NFATc1) is involved in upregulating slow myosin heavy chain (MHC) gene expression during fast-to-slow transformation of skeletal muscle cells. This study aims to investigate the Ca2+ signal necessary to activate the calcineurin-NFATc1 cascade in skeletal muscle. Electrostimulation of primary myocytes from rabbit for 24 h induced a distinct fast-to-slow transformation at the MHC mRNA level and a full activation of the calcineurin-NFATc1 pathway, although resting Ca2+ concentration ([Ca2+]i) remained unaltered at 70 nM. During activation, the calcium transients of these myocytes reach a peak concentration of ~500 nM. Although 70 nM [Ca2+]i does not activate calcineurin-NFAT, we show by the use of Ca2+ ionophore that the system is fully activated when [Ca2+]i is >=150 nM in a sustained manner. We conclude that the calcineurin signal transduction pathway and the slow MHC gene in cultured skeletal muscle cells are activated by repetition of the rapid high-amplitude calcium transients that are associated with excitation-contraction coupling rather than by a sustained elevation of resting Ca2+ concentration.

muscle plasticity; NFATc1; resting calcium concentration



Address for reprint requests and other correspondence: H.-P. Kubis, Zentrum Physiologie, Medizinische Hochschule Hannover, D-30625 Hannover, Germany, (E-mail: Kubis.HansP{at}mh-hannover.de).




This article has been cited by other articles:


Home page
FASEB J.Home page
J. T. Lanner, J. D. Bruton, Y. Assefaw-Redda, Z. Andronache, S.-J. Zhang, D. Severa, Z.-B. Zhang, W. Melzer, S.-L. Zhang, A. Katz, et al.
Knockdown of TRPC3 with siRNA coupled to carbon nanotubes results in decreased insulin-mediated glucose uptake in adult skeletal muscle cells
FASEB J, June 1, 2009; 23(6): 1728 - 1738.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
W. A. LaFramboise, R. C. Jayaraman, K. L. Bombach, D. P. Ankrapp, J. M. Krill-Burger, C. M. Sciulli, P. Petrosko, and R. W. Wiseman
Acute molecular response of mouse hindlimb muscles to chronic stimulation
Am J Physiol Cell Physiol, January 1, 2009; 297(3): C556 - C570.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
J. A. Drenning, V. A. Lira, C. G. Simmons, Q. A. Soltow, J. E. Sellman, and D. S. Criswell
Nitric oxide facilitates NFAT-dependent transcription in mouse myotubes
Am J Physiol Cell Physiol, April 1, 2008; 294(4): C1088 - C1095.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
J. A. Valdes, E. Gaggero, J. Hidalgo, N. Leal, E. Jaimovich, and M. A. Carrasco
NFAT activation by membrane potential follows a calcium pathway distinct from other activity-related transcription factors in skeletal muscle cells
Am J Physiol Cell Physiol, March 1, 2008; 294(3): C715 - C725.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
N. Dehne, U. Kerkweg, T. Otto, and J. Fandrey
The HIF-1 response to simulated ischemia in mouse skeletal muscle cells neither enhances glycolysis nor prevents myotube cell death
Am J Physiol Regulatory Integrative Comp Physiol, October 1, 2007; 293(4): R1693 - R1701.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
X. Mu, L. D. Brown, Y. Liu, and M. F. Schneider
Roles of the calcineurin and CaMK signaling pathways in fast-to-slow fiber type transformation of cultured adult mouse skeletal muscle fibers
Physiol Genomics, August 20, 2007; 30(3): 300 - 312.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
Y.-C. Huang, R. G. Dennis, and K. Baar
Cultured slow vs. fast skeletal muscle cells differ in physiology and responsiveness to stimulation
Am J Physiol Cell Physiol, July 1, 2006; 291(1): C11 - C17.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
J. V. Chakkalakal, S. A. Michel, E. R. Chin, R. N. Michel, and B. J. Jasmin
Targeted inhibition of Ca2+/calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle
Hum. Mol. Genet., May 1, 2006; 15(9): 1423 - 1435.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
S. L. McGee and M. Hargreaves
Exercise and Myocyte Enhancer Factor 2 Regulation in Human Skeletal Muscle
Diabetes, May 1, 2004; 53(5): 1208 - 1214.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
P. G. Hogan, L. Chen, J. Nardone, and A. Rao
Transcriptional regulation by calcium, calcineurin, and NFAT
Genes & Dev., September 15, 2003; 17(18): 2205 - 2232.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2003 by the American Physiological Society.