Lee Seunghwan, Briklin Olga, Hiel Hakim, Fuchs Paul
Department of Otolaryngology - Head & Neck Surgery, Hanyang University, Seoul, Korea.
J Physiol. 2007 Sep 15;583(Pt 3):909-22. doi: 10.1113/jphysiol.2007.135582. Epub 2007 Jul 26.
Voltage-gated calcium channels support both spontaneous and sound-evoked neurotransmitter release from ribbon synapses of cochlear hair cells. A variety of regulatory mechanisms must cooperate to ensure the appropriate level of activity in the restricted pool of synaptic calcium channels ( approximately 100) available to each synaptic ribbon. One potential feedback mechanism, calcium-dependent inactivation (CDI) of voltage-gated, L-type calcium channels, can be modulated by calmodulin-like calcium-binding proteins. CDI of voltage-gated calcium current was studied in hair cells of the chicken's basilar papilla (analogous to the mammalian cochlea) after blocking the predominant potassium conductances. For inactivating currents produced by 2.5 s steps to the peak of the current-voltage relation (1 mm EGTA internal calcium buffer), single exponential fits yielded an average decay time constant of 1.92 +/- 0.18 s (mean +/- s.e.m., n = 12) at 20-22 degrees C, while recovery occurred with a half-time of approximately 10 s. Inactivation produced no change in reversal potential, arguing that the observed relaxation did not result from alternative processes such as calcium accumulation or activation of residual potassium currents. Substitution of external calcium with barium greatly reduced inactivation, while inhibition of endoplasmic calcium pumps with t-benzohydroquinone (BHQ) or thapsigargin made inactivation occur faster and to a greater extent. Raising external calcium 10-fold (from 2 to 20 mm) increased peak current 3-fold, but did not alter the extent or time course of CDI. However, increasing levels of internal calcium buffer consistently reduced the rate and extent of inactivation. With 1 mm EGTA buffering and in 2 mm external calcium, the available pool of calcium channels was half-inactivated near the resting membrane potential (-50 mV). CDI may be further regulated by calmodulin-like calcium-binding proteins (CaBPs). mRNAs for several CaBPs are expressed in chicken cochlear tissue, and antibodies to CaBP4 label hair cells, but not supporting cells, equivalent to the pattern seen in mammalian cochlea. Thus, molecular mechanisms that underlie CDI appeared to be conserved across vertebrate species, may provide a means to adjust calcium channel open probability, and could serve to maintain the set-point for spontaneous release from the ribbon synapse.
电压门控钙通道支持耳蜗毛细胞带状突触的自发和声音诱发的神经递质释放。多种调节机制必须协同作用,以确保每个突触带可用的有限数量(约100个)突触钙通道的适当活性水平。一种潜在的反馈机制,即电压门控L型钙通道的钙依赖性失活(CDI),可由钙调蛋白样钙结合蛋白调节。在阻断主要的钾电导后,研究了鸡基底乳头(类似于哺乳动物的耳蜗)毛细胞中电压门控钙电流的CDI。对于由2.5秒的阶跃到电流-电压关系峰值(1 mM EGTA内部钙缓冲液)产生的失活电流,在20-22摄氏度下,单指数拟合得到的平均衰减时间常数为1.92±0.18秒(平均值±标准误,n = 12),而恢复的半衰期约为10秒。失活不会使反转电位发生变化,这表明观察到的松弛不是由钙积累或残余钾电流激活等其他过程引起的。用钡替代外部钙可大大降低失活,而用叔丁基对苯二酚(BHQ)或毒胡萝卜素抑制内质网钙泵会使失活发生得更快且程度更大。将外部钙浓度提高10倍(从2 mM提高到20 mM)可使峰值电流增加3倍,但不会改变CDI的程度或时间进程。然而,增加内部钙缓冲液的水平会持续降低失活的速率和程度。在1 mM EGTA缓冲和2 mM外部钙的条件下,钙通道的可用池在静息膜电位(-50 mV)附近被半失活。CDI可能会受到钙调蛋白样钙结合蛋白(CaBP)的进一步调节。几种CaBP的mRNA在鸡耳蜗组织中表达,针对CaBP4的抗体标记毛细胞,但不标记支持细胞,这与在哺乳动物耳蜗中看到的模式相同。因此,CDI的分子机制似乎在脊椎动物物种中是保守的,可能提供一种调节钙通道开放概率的方法,并有助于维持带状突触自发释放的设定点。