Engisch K L, Nowycky M C
Department of Neurobiology and Anatomy, Medical College of Pennsylvania, Philadelphia 19129, USA.
J Neurosci. 1996 Feb 15;16(4):1359-69. doi: 10.1523/JNEUROSCI.16-04-01359.1996.
We used the perforated-patch technique to examine the relationship between Ca2+ entry and exocytosis of large dense-cored vesicles in bovine adrenal chromaffin cells. Exocytosis evoked by single-step depolarizations was monitored by capacitance detection. Ca2+ entry was varied by changing external calcium concentration, stepping to different test potentials, depolarizing for different durations, or applying blockers of specific calcium channel subtypes. Regardless of protocol, the amount of exocytosis was strictly related to the integral of the voltage-clamped calcium current, raised to a power of approximately 1.5. Thus, despite the complexities of transient and nonuniform changes in submembrane calcium concentration produced by voltage-gated calcium entry, the calcium dependence of large dense-cored vesicle fusion under conditions of minimal stimulation is well approximated by a simple transfer function of summed calcium entry.
我们采用穿孔膜片钳技术研究了牛肾上腺嗜铬细胞中钙离子内流与大致密核心囊泡胞吐作用之间的关系。通过电容检测监测单步去极化诱发的胞吐作用。通过改变细胞外钙浓度、切换到不同的测试电位、进行不同时长的去极化或应用特定钙通道亚型的阻滞剂来改变钙离子内流。无论采用何种方案,胞吐作用的量都与电压钳制的钙电流积分严格相关,该积分被提升至约1.5的幂次。因此,尽管电压门控钙内流产生的膜下钙浓度存在瞬态和非均匀变化的复杂性,但在最小刺激条件下,大致密核心囊泡融合的钙依赖性可以通过简单的总钙内流传递函数很好地近似。