Functional expression of the L-type calcium channel in mice skeletal muscle during prenatal myogenesis

被引:13
作者
Strube, C
Tourneur, Y
Ojeda, C
机构
[1] Lab Physiol Elements Excitables, CNRS, UMR 5578, UCB Lyon 1, F-69622 Villeurbanne, France
[2] INSERM, U121, F-69500 Bron, France
关键词
D O I
10.1016/S0006-3495(00)76684-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The densities of skeletal muscle intramembrane charge movement and macroscopic L-type Ca2+ current have been shown to increase during prenatal development. In the present work, the electrophysiological characteristics of L-type Ca2+ 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 Ca2+ 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 Ca2+ 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.
引用
收藏
页码:1282 / 1292
页数:11
相关论文
共 50 条
[21]   Functional coupling between CAV1.2 L-type calcium channel and calcium sparks in smooth muscle [J].
Moosmang, S ;
Essine, K ;
Schulla, V ;
Welling, A ;
Feil, R ;
Gollasch, M ;
Hofmann, F .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2004, 369 :R58-R58
[22]   Norepinephrine regulates the in vivo expression of the L-type calcium channel [J].
Golden, KL ;
Ren, J ;
Dean, A ;
Marsh, JD .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 236 (1-2) :107-114
[23]   Expression of the L-type calcium channel in human heart failure [J].
Joachim Hersel ;
Simon Jung ;
Paul Mohacsi ;
Roger Hullin .
Basic Research in Cardiology, 2002, 97 (Suppl 1) :I4-I10
[24]   Norepinephrine regulates the in vivo expression of the L-type calcium channel [J].
Kish L. Golden ;
Jun Ren ;
Andrea Dean ;
James D. Marsh .
Molecular and Cellular Biochemistry, 2002, 236 :107-114
[25]   L-type calcium channel expression depends on the differentiated state of vascular smooth muscle cells [J].
Gollasch, M ;
Haase, H ;
Ried, C ;
Lindschau, C ;
Morano, I ;
Luft, FC ;
Haller, H .
FASEB JOURNAL, 1998, 12 (07) :593-601
[26]   Effects of cyclosporine A on vascular smooth muscle L-type calcium channel activity and gene expression [J].
Tharp, DL ;
Wamhoff, BR ;
Bowles, DK .
FASEB JOURNAL, 2004, 18 (05) :A1238-A1239
[27]   Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice [J].
Friedrich, O ;
Both, M ;
Gillis, JM ;
Chamberlain, JS ;
Fink, RHA .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 555 (01) :251-265
[28]   Thyroid hormone increased L-type calcium channel mRNA expression and L-type calcium current of myocytes in rabbits [J].
Yu, Zhui ;
Wang, Teng ;
Xu, Lin ;
Huang, Cong-xin .
BIO-MEDICAL MATERIALS AND ENGINEERING, 2012, 22 (1-3) :49-55
[29]   L-type calcium channel regulation of abnormal tyrosine hydroxylase expression in cerebella of tottering mice [J].
Fureman, BE ;
Campbell, DB ;
Hess, EJ .
MOLECULAR AND FUNCTIONAL DIVERSITY OF ION CHANNELS AND RECEPTORS, 1999, 868 :217-219
[30]   Increased expression of the cardiac L-type calcium channel in estrogen receptor-deficient mice [J].
Johnson, BD ;
Zheng, W ;
Korach, KS ;
Scheuer, T ;
Catterall, WA ;
Rubanyi, GM .
JOURNAL OF GENERAL PHYSIOLOGY, 1997, 110 (02) :135-140