首页> 美国卫生研究院文献>The Journal of Neuroscience >ATP-Induced Ca2+ Release in Cochlear Outer Hair Cells: Localization of an Inositol Triphosphate-Gated Ca2+ Store to the Base of the Sensory Hair Bundle
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ATP-Induced Ca2+ Release in Cochlear Outer Hair Cells: Localization of an Inositol Triphosphate-Gated Ca2+ Store to the Base of the Sensory Hair Bundle

机译:耳蜗外毛细胞中ATP诱导的Ca2 +释放:三磷酸肌醇门控的Ca2 +储存在感官发束底部的定位。

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摘要

We used a high-performance fluorescence imaging system to visualize rapid changes in intracellular free Ca2+concentration ([Ca2+]i) evoked by focal applications of extracellular ATP to the hair bundle of outer hair cells (OHCs): the sensory–motor receptors of the cochlea. Simultaneous recordings of the whole-cell current and Calcium Green-1 fluorescence showed a two-component increase in [Ca2+]i. After an initial entry of Ca2+ through the apical membrane, a second and larger, inositol triphosphate (InsP3)-gated, [Ca2+]i surge occurred at the base of the hair bundle. Electron microscopy of this intracellular Ca2+ release site showed that it coincides with the localization of a unique system of endoplasmic reticulum (ER) membranes and mitochondria known as Hensen’s body. Using confocal immunofluorescence microscopy, we showed that InsP3receptors share this location. Consistent with a Ca2+-mobilizing second messenger system linked to ATP-P2 receptors, we also determined that an isoform of G-proteins is present in the stereocilia. Voltage-driven cell shape changes and nonlinear capacitance were monitored before and after ATP application, showing that the ATP-evoked [Ca2+]irise did not interfere with the OHC electromotility mechanism. This second messenger signaling mechanism bypasses the Ca2+-clearance power of the stereocilia and transiently elevates [Ca2+]i at the base of the hair bundle, where it can potentially modulate the action of unconventional myosin isozymes involved in maintaining the hair bundle integrity and potentially influence mechanotransduction.
机译:我们使用高性能的荧光成像系统来观察细胞外ATP集中应用引起的细胞内游离Ca 2 + i([Ca 2 + ] i)浓度的快速变化。外毛细胞(OHCs)的发束:耳蜗的感觉运动受体。全细胞电流和Calcium Green-1荧光的同时记录显示[Ca 2 + ] i增加了两个分量。 Ca 2 + 最初通过顶膜进入后,第二个更大的肌醇三磷酸(InsP3)门控的[Ca 2 + ] i激增发生在发束的基部。电子显微镜观察到该细胞内Ca 2 + 释放位点表明,它与内质网(ER)膜和线粒体(称为Hensen的身体)的独特系统的定位相吻合。使用共聚焦免疫荧光显微镜,我们显示InsP3受体共享此位置。与连接到ATP-P2受体的Ca 2 + 动员第二信使系统相一致,我们还确定了立体纤毛中存在G蛋白的同工型。 ATP施加前后监测电压驱动的细胞形状变化和非线性电容,表明ATP诱发的[Ca 2 + ] irise不会干扰OHC电动势机制。第二个Messenger信号传导机制绕过了纤毛的Ca 2 + 清除能力,并在发束的底部暂时升高了[Ca 2 + ] i,可能调节非常规肌球蛋白同工酶的作用,参与维持发束完整性,并可能影响机械传导。

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