García J, Tanabe T, Beam K G
Department of Physiology, Colorado State University, Fort Collins 80523.
J Gen Physiol. 1994 Jan;103(1):125-47. doi: 10.1085/jgp.103.1.125.
In both skeletal and cardiac muscle, the dihydropyridine (DHP) receptor is a critical element in excitation-contraction (e-c) coupling. However, the mechanism for calcium release is completely different in these muscles. In cardiac muscle the DHP receptor functions as a rapidly-activated calcium channel and the influx of calcium through this channel induces calcium release from the sarcoplasmic reticulum (SR). In contrast, in skeletal muscle the DHP receptor functions as a voltage sensor and as a slowly-activating calcium channel; in this case, the voltage sensor controls SR calcium release. It has been previously demonstrated that injection of dysgenic myotubes with cDNA (pCAC6) encoding the skeletal muscle DHP receptor restores the slow calcium current and skeletal type e-c coupling that does not require entry of external calcium (Tanabe, Beam, Powell, and Numa. 1988. Nature. 336:134-139). Furthermore, injection of cDNA (pCARD1) encoding the cardiac DHP receptor produces rapidly activating calcium current and cardiac type e-c coupling that does require calcium entry (Tanabe, Mikami, Numa, and Beam. 1990. Nature. 344:451-453). In this paper, we have studied the voltage dependence of, and the relationship between, charge movement, calcium transients, and calcium current in normal skeletal muscle cells in culture. In addition, we injected pCAC6 or pCARD1 into the nuclei of dysgenic myotubes and studied the relationship between the restored events and compared them with those of the normal cells. Charge movement and calcium currents were recorded with the whole cell patch-clamp technique. Calcium transients were measured with Fluo-3 introduced through the patch pipette. The kinetics and voltage dependence of the charge movement, calcium transients, and calcium current in dysgenic myotubes expressing pCAC6 were qualitatively similar to the ones elicited in normal myotubes: the calcium transient displayed a sigmoidal dependence on voltage and was still present after the addition of 0.5 mM Cd2+ + 0.1 mM La3+. In contrast, the calcium transient in dysgenic myotubes expressing pCARD1 followed the amplitude of the calcium current and thus showed a bell shaped dependence on voltage. In addition, the transient had a slower rate of rise than in pCAC6-injected myotubes and was abolished completely by the addition of Cd2+ + La3+.
在骨骼肌和心肌中,二氢吡啶(DHP)受体都是兴奋-收缩(e-c)偶联的关键元件。然而,这两种肌肉中钙释放的机制却完全不同。在心肌中,DHP受体作为快速激活的钙通道发挥作用,通过该通道的钙内流诱导肌浆网(SR)释放钙。相比之下,在骨骼肌中,DHP受体作为电压传感器和缓慢激活的钙通道发挥作用;在这种情况下,电压传感器控制SR钙释放。先前已证明,向发育不全的肌管中注射编码骨骼肌DHP受体的cDNA(pCAC6)可恢复缓慢的钙电流和不需要外部钙进入的骨骼肌型e-c偶联(田边、比姆、鲍威尔和沼田。1988年。《自然》。336:134 - 139)。此外,注射编码心脏DHP受体的cDNA(pCARD1)会产生确实需要钙进入的快速激活钙电流和心脏型e-c偶联(田边、三上、沼田和比姆。1990年。《自然》。344:451 - 453)。在本文中,我们研究了培养的正常骨骼肌细胞中电荷移动、钙瞬变和钙电流的电压依赖性以及它们之间的关系。此外,我们将pCAC6或pCARD1注射到发育不全肌管的细胞核中,研究恢复事件之间的关系,并将它们与正常细胞的进行比较。用全细胞膜片钳技术记录电荷移动和钙电流。通过膜片吸管引入Fluo - 3来测量钙瞬变。表达pCAC6的发育不全肌管中电荷移动、钙瞬变和钙电流的动力学及电压依赖性在质量上与正常肌管中引发的相似:钙瞬变对电压呈S形依赖性,并且在添加0.5 mM Cd2 + + 0.1 mM La3 +后仍然存在。相比之下,表达pCARD1的发育不全肌管中的钙瞬变跟随钙电流的幅度,因此对电压呈钟形依赖性。此外,该瞬变的上升速率比注射pCAC6的肌管中的慢,并且在添加Cd2 + + La3 +后完全消失。