共 93 条
Bridging the myoplasmic gap II: more recent advances in skeletal muscle excitation-contraction coupling
被引:26
作者:

Bannister, Roger A.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Colorado, Dept Med, Div Cardiol, Denver Anschutz Med Campus,12700 East 19th Ave,Ro, Aurora, CO 80045 USA Univ Colorado, Dept Med, Div Cardiol, Denver Anschutz Med Campus,12700 East 19th Ave,Ro, Aurora, CO 80045 USA
机构:
[1] Univ Colorado, Dept Med, Div Cardiol, Denver Anschutz Med Campus,12700 East 19th Ave,Ro, Aurora, CO 80045 USA
关键词:
1,4-dihydropyridine receptor;
DHPR;
Ca(V)1.1;
alpha S-1;
L-type;
Excitation-contraction coupling;
Skeletal muscle;
RECEPTOR BETA-1A SUBUNIT;
CALCIUM-RELEASE CHANNEL;
C-TERMINAL TAIL;
DIHYDROPYRIDINE-RECEPTOR;
CA2+ CHANNEL;
RYANODINE RECEPTORS;
BETA(1A) SUBUNIT;
CRYSTAL-STRUCTURES;
CHARGE MOVEMENT;
CARBOXYL-TERMINUS;
D O I:
10.1242/jeb.124123
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
In skeletal muscle, excitation-contraction (EC) coupling relies on the transmission of an intermolecular signal from the voltage-sensing regions of the L-type Ca2+ channel (Ca(V)1.1) in the plasma membrane to the channel pore of the type 1 ryanodine receptor (RyR1) nearly 10 nm away in the membrane of the sarcoplasmic reticulum (SR). Even though the roles of Ca(V)1.1 and RyR1 as voltage sensor and SR Ca2+ release channel, respectively, have been established for nearly 25 years, the mechanism underlying communication between these two channels remains undefined. In the course of this article, I will review current viewpoints on this topic with particular emphasis on recent studies.
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页码:175 / 182
页数:8
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