Gera S, Byerly L
Department of Biological Sciences, University of Southern California, Los Angeles, California 90089-2520, USA.
J Gen Physiol. 1999 Oct;114(4):535-50. doi: 10.1085/jgp.114.4.535.
Ca(2+) channel inactivation in the neurons of the freshwater snail, Lymnaea stagnalis, was studied using patch-clamp techniques. In the presence of a high concentration of intracellular Ca(2+) buffer (5 mM EGTA), the inactivation of these Ca(2+) channels is entirely voltage dependent; it is not influenced by the identity of the permeant divalent ions or the amount of extracellular Ca(2+) influx, or reduced by higher levels of intracellular Ca(2+) buffering. Inactivation measured under these conditions, despite being independent of Ca(2+) influx, has a bell-shaped voltage dependence, which has often been considered a hallmark of Ca(2+)-dependent inactivation. Ca(2+)-dependent inactivation does occur in Lymnaea neurons, when the concentration of the intracellular Ca(2+) buffer is lowered to 0.1 mM EGTA. However, the magnitude of Ca(2+)-dependent inactivation does not increase linearly with Ca(2+) influx, but saturates for relatively small amounts of Ca(2+) influx. Recovery from inactivation at negative potentials is biexponential and has the same time constants in the presence of different intracellular concentrations of EGTA. However, the amplitude of the slow component is selectively enhanced by a decrease in intracellular EGTA, thus slowing the overall rate of recovery. The ability of 5 mM EGTA to completely suppress Ca(2+)-dependent inactivation suggests that the Ca(2+) binding site is at some distance from the channel protein itself. No evidence was found of a role for serine/threonine phosphorylation in Ca(2+) channel inactivation. Cytochalasin B, a microfilament disrupter, was found to greatly enhance the amount of Ca(2+) channel inactivation, but the involvement of actin filaments in this effect of cytochalasin B on Ca(2+) channel inactivation could not be verified using other pharmacological compounds. Thus, the mechanism of Ca(2+)-dependent inactivation in these neurons remains unknown, but appears to differ from those proposed for mammalian L-type Ca(2+) channels.
利用膜片钳技术研究了淡水螺椎实螺神经元中Ca(2+)通道的失活情况。在高浓度细胞内Ca(2+)缓冲剂(5 mM EGTA)存在的情况下,这些Ca(2+)通道的失活完全依赖于电压;它不受通透二价离子的种类、细胞外Ca(2+)内流的量的影响,也不会因更高水平的细胞内Ca(2+)缓冲作用而降低。在这些条件下测得的失活,尽管与Ca(2+)内流无关,但具有钟形的电压依赖性,这通常被认为是Ca(2+)依赖性失活的一个标志。当细胞内Ca(2+)缓冲剂的浓度降至0.1 mM EGTA时,椎实螺神经元中确实会发生Ca(2+)依赖性失活。然而,Ca(2+)依赖性失活的程度并不随Ca(2+)内流呈线性增加,而是在相对少量的Ca(2+)内流时就达到饱和。在负电位下从失活状态恢复是双指数的,并且在不同细胞内EGTA浓度存在时具有相同的时间常数。然而,细胞内EGTA减少会选择性地增强慢成分的幅度,从而减慢整体恢复速率。5 mM EGTA完全抑制Ca(2+)依赖性失活的能力表明,Ca(2+)结合位点与通道蛋白本身有一定距离。未发现丝氨酸/苏氨酸磷酸化在Ca(2+)通道失活中起作用的证据。细胞松弛素B,一种微丝破坏剂,被发现能大大增强Ca(2+)通道失活的量,但使用其他药理化合物无法证实肌动蛋白丝参与了细胞松弛素B对Ca(2+)通道失活的这种作用。因此,这些神经元中Ca(2+)依赖性失活的机制仍然未知,但似乎与哺乳动物L型Ca(2+)通道所提出的机制不同。