Biology Department, University of Massachusetts Amherst, Amherst, Massachusetts 01003.
Molecular and Cellular Biology Graduate Program, University of Massachusetts Amherst, Amherst, Massachusetts 01003.
J Neurosci. 2021 Feb 24;41(8):1625-1635. doi: 10.1523/JNEUROSCI.1324-18.2020. Epub 2021 Jan 14.
Proper perception of sounds in the environment requires auditory signals to be encoded with extraordinary temporal precision up to tens of microseconds, but how it originates from the hearing organs in the periphery is poorly understood. In particular, sound-evoked spikes in auditory afferent fibers are phase-locked to sound frequencies up to 5 kHz, but it is not clear how hair cells can handle intracellular Ca changes with such high speed and efficiency. In this study, we combined patch-clamp recording and two-photon Ca imaging to examine Ca dynamics in hair cell ribbon synapses in the bullfrog amphibian papilla of both sexes. We found that Ca clearance from single synaptic ribbons followed a double exponential function, and the weight of the fast component, but not the two time constants, was significantly reduced for prolonged stimulation, and during inhibition of the plasma membrane Ca ATPase (PMCA), the mitochondrial Ca uptake (MCU), or the sarcolemma/endoplasmic reticulum Ca ATPase (SERCA), but not the Na/Ca exchanger (NCX). Furthermore, we found that both the basal Ca level and the Ca rise during sinusoidal stimulation were significantly increased by inhibition of PMCA, MCU, or SERCA. Consistently, phase-locking of synaptic vesicle releases from hair cells was also significantly reduced by blocking PMCA, MCU, or SERCA, but not NCX. We conclude that, in addition to fast diffusion mediated by mobile Ca buffer, multiple Ca extrusion pumps are required for phase-locking at the auditory hair cell ribbon synapse. Hair cell synapses can transmit sound-driven signals precisely in the kHz range. However, previous studies of Ca handling in auditory hair cells have often been conducted in immature hair cells, with elevated extracellular Ca concentration, or through steady-state stimulation that may not be physiologically relevant. Here we examine Ca clearance from hair cell synaptic ribbons in a fully mature preparation at physiological concentration of external Ca and at physiological temperature. By stimulating hair cells with sinusoidal voltage commands that mimic pure sound tones, we recapitulated the phase-locking of hair cell exocytosis with an approach. This allowed us to reveal the Ca extrusion mechanisms that are required for phase-locking at auditory hair cell ribbon synapses.
环境中声音的适当感知需要听觉信号以高达数十微秒的极高时间精度进行编码,但听觉器官如何在周围产生这种信号还知之甚少。特别是,听觉传入纤维中的声音诱发尖峰与高达 5 kHz 的声音频率锁相,但尚不清楚毛细胞如何以如此高的速度和效率处理细胞内 Ca 变化。在这项研究中,我们结合了膜片钳记录和双光子 Ca 成像技术,研究了两性牛蛙听觉器官的毛细胞带状突触中的 Ca 动力学。我们发现,单个突触带的 Ca 清除遵循双指数函数,并且快速分量的权重,但不是两个时间常数,在长时间刺激和抑制质膜 Ca-ATP 酶 (PMCA)、线粒体 Ca 摄取 (MCU) 或肌质网膜/内质网 Ca-ATP 酶 (SERCA) 时显著降低,但不降低 Na/Ca 交换体 (NCX)。此外,我们发现抑制 PMCA、MCU 或 SERCA 会显著增加基础 Ca 水平和正弦刺激期间的 Ca 上升。一致地,阻断 PMCA、MCU 或 SERCA 也会显著降低毛细胞从带状突触释放突触囊泡的锁相,而阻断 NCX 则不会。我们得出的结论是,除了由可移动 Ca 缓冲剂介导的快速扩散外,多个 Ca 外排泵对于听觉毛细胞带状突触的锁相也是必需的。毛细胞突触可以在 kHz 范围内精确传递声音驱动的信号。然而,先前关于听觉毛细胞 Ca 处理的研究通常是在成熟度较低的毛细胞中进行的,细胞外 Ca 浓度升高,或通过稳态刺激进行,这可能与生理无关。在这里,我们在生理浓度的外 Ca 和生理温度下研究毛细胞突触带上的 Ca 清除。通过用模拟纯音的正弦电压命令刺激毛细胞,我们用一种新颖的方法再现了毛细胞胞吐的锁相。这使我们能够揭示听觉毛细胞带状突触锁相所需的 Ca 外排机制。