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Electrical tuning and transduction in short hair cells of the chicken auditory papilla

机译:鸡听觉乳头短毛细胞的电调节和转导

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摘要

The avian auditory papilla contains two classes of sensory receptor, tall hair cells (THCs) and short hair cells (SHCs), the latter analogous to mammalian outer hair cells with large efferent but sparse afferent innervation. Little is known about the tuning, transduction, or electrical properties of SHCs. To address this problem, we made patch-clamp recordings from hair cells in an isolated chicken basilar papilla preparation at 33°C. We found that SHCs are electrically tuned by a Ca2+-activated K+ current, their resonant frequency varying along the papilla in tandem with that of the THCs, which also exhibit electrical tuning. The tonotopic map for THCs was similar to maps previously described from auditory nerve fiber measurements. SHCs also possess an A-type K+ current, but electrical tuning was observed only at resting potentials positive to −45 mV, where the A current is inactivated. We predict that the resting potential in vivo is approximately −40 mV, depolarized by a standing inward current through mechanotransducer (MT) channels having a resting open probability of ∼0.26. The resting open probability stems from a low endolymphatic Ca2+ concentration (0.24 mM) and a high intracellular mobile Ca2+ buffer concentration, estimated from perforated-patch recordings as equivalent to 0.5 mM BAPTA. The high buffer concentration was confirmed by quantifying parvalbumin-3 and calbindin D-28K with calibrated postembedding immunogold labeling, demonstrating >1 mM calcium-binding sites. Both proteins displayed an apex-to-base gradient matching that in the MT current amplitude, which increased exponentially along the papilla. Stereociliary bundles also labeled heavily with antibodies against the Ca2+ pump isoform PMCA2a.
机译:禽听觉乳头包含两类感觉受体:高毛细胞(THC)和短毛细胞(SHC),后者类似于具有大量传入但稀疏传入神经的哺乳动物外毛细胞。关于SHC的调谐,传导或电学性质知之甚少。为了解决这个问题,我们在33°C的分离的鸡基底乳头制品中从毛细胞中制作了膜片钳录音。我们发现SHCs由Ca 2 + 激活的K + 电流进行电调谐,其共振频率沿乳头与THC一致,并表现出电调。 THC的色调图类似于先前从听神经纤维测量中描述的图。 SHC还具有A型K + 电流,但仅在正电流为-45 mV的静止电位下观察到电调谐,此时A电流被灭活。我们预测体内的静息电位约为-40 mV,通过静力通过机械换能器(MT)通道的静向内流去极化,静息打开概率约为0.26。静息开放概率来自低内淋巴Ca 2 + 浓度(0.24 mM)和高细胞内移动Ca 2 + 缓冲液浓度,根据穿孔斑片记录估计为等效浓度到0.5 mM BAPTA。通过用校准的包埋后免疫金标记对parvalbumin-3和calbindin D-28K进行定量,证实了高缓冲液浓度,证实了> 1 mM的钙结合位点。两种蛋白质都显示出与MT电流振幅相匹配的从顶点到碱基的梯度,该梯度沿乳头呈指数增加。立体声束还用抗Ca 2 + 泵同工型PMCA2a的抗体标记很重。

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