» Articles » PMID: 10692316

Functional Expression of the L-type Calcium Channel in Mice Skeletal Muscle During Prenatal Myogenesis

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2000 Feb 29
PMID 10692316
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

The densities of skeletal muscle intramembrane charge movement and macroscopic L-type Ca(2+) current have been shown to increase during prenatal development. In the present work, the electrophysiological characteristics of L-type Ca(2+) channels were analyzed over the embryonic period E14 to E19 using the whole-cell and cell-attached procedures. At the macroscopic level, the whole-cell L-type Ca(2+) conductance increased 100% between E14 and E19. This enhancement was accompanied by a small negative shift of the voltage dependence and a marked acceleration of the inactivation kinetics. At the single-channel level, the unitary conductance decreased significantly from 13.2 +/- 0.1 pS (n = 8) at E14 to 10.7 +/- 0.3 pS (n = 7) at E18 and the open probability was multiplied by 2. No significant change of the density of functional channels was observed during the same period. In contrast to the density of intramembrane charge movement, which, under the same conditions, has been shown to increase between 16 and 19 days, L-type Ca(2+) channels properties change mostly between 14 and 16 days. Taken together, these results suggest that the two functions of the dihydropyridine receptor are carried by two different proteins which could be differentially regulated by subunit composition and/or degree of phosphorylation.

Citing Articles

Anaesthetic tricaine acts preferentially on neural voltage-gated sodium channels and fails to block directly evoked muscle contraction.

Attili S, Hughes S PLoS One. 2014; 9(8):e103751.

PMID: 25090007 PMC: 4121177. DOI: 10.1371/journal.pone.0103751.


Absence of regulation of the T-type calcium current by Cav1.1, beta1a and gamma1 dihydropyridine receptor subunits in skeletal muscle cells.

Strube C Pflugers Arch. 2007; 455(5):921-7.

PMID: 17906876 DOI: 10.1007/s00424-007-0345-9.


Ca2+ channel regulation by transforming growth factor-beta 1 and bone morphogenetic protein-2 in developing mice myotubes.

Mejia-Luna L, Avila G J Physiol. 2004; 559(Pt 1):41-54.

PMID: 15218061 PMC: 1665083. DOI: 10.1113/jphysiol.2004.066852.


Low-voltage-activated ("T-Type") calcium channels in review.

Yunker A, McEnery M J Bioenerg Biomembr. 2004; 35(6):533-75.

PMID: 15000520 DOI: 10.1023/b:jobb.0000008024.77488.48.


Membrane cholesterol modulates dihydropyridine receptor function in mice fetal skeletal muscle cells.

Pouvreau S, Berthier C, Blaineau S, Amsellem J, Coronado R, Strube C J Physiol. 2004; 555(Pt 2):365-81.

PMID: 14724204 PMC: 1664851. DOI: 10.1113/jphysiol.2003.055285.


References
1.
Singer D, Biel M, Lotan I, Flockerzi V, Hofmann F, Dascal N . The roles of the subunits in the function of the calcium channel. Science. 1991; 253(5027):1553-7. DOI: 10.1126/science.1716787. View

2.
Franzini-Armstrong C . Simultaneous maturation of transverse tubules and sarcoplasmic reticulum during muscle differentiation in the mouse. Dev Biol. 1991; 146(2):353-63. DOI: 10.1016/0012-1606(91)90237-w. View

3.
Strube C, Bournaud R, Inoue I, Shimahara T . Intramembrane charge movement in developing skeletal muscle cells from fetal mice. Pflugers Arch. 1992; 421(6):572-7. DOI: 10.1007/BF00375053. View

4.
Chaudhari N, Beam K . mRNA for cardiac calcium channel is expressed during development of skeletal muscle. Dev Biol. 1993; 155(2):507-15. DOI: 10.1006/dbio.1993.1048. View

5.
McDONALD T, Pelzer S, TRAUTWEIN W, Pelzer D . Regulation and modulation of calcium channels in cardiac, skeletal, and smooth muscle cells. Physiol Rev. 1994; 74(2):365-507. DOI: 10.1152/physrev.1994.74.2.365. View