首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >ATP-Induced Ca(2+) release in cochlear outer hair cells: localization of an inositol triphosphate-gated Ca(2+) store to the base of the sensory hair bundle.
【24h】

ATP-Induced Ca(2+) release in cochlear outer hair cells: localization of an inositol triphosphate-gated Ca(2+) store to the base of the sensory hair bundle.

机译:耳蜗外毛细胞中ATP诱导的Ca(2+)释放:肌醇三磷酸门控的Ca(2+)存储到感官发束的底部的定位。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

We used a high-performance fluorescence imaging system to visualize rapid changes in intracellular free Ca(2+) concentration ([Ca(2+)](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 [Ca(2+)](i). After an initial entry of Ca(2+) through the apical membrane, a second and larger, inositol triphosphate (InsP(3))-gated, [Ca(2+)](i) surge occurred at the base of the hair bundle. Electron microscopy of this intracellular Ca(2+) 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 InsP(3) receptors share this location. Consistent with a Ca(2+)-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 [Ca(2+)](i) rise did not interfere with the OHC electromotility mechanism. This second messenger signaling mechanism bypasses the Ca(2+)-clearance power of the stereocilia and transiently elevates [Ca(2+)](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:我们使用了高性能的荧光成像系统来可视化细胞外游离Ca(2+)浓度([Ca(2 +)](i))的迅速变化,该变化是由细胞外ATP对外部毛细胞的发束的聚焦应用引起的( OHCs):耳蜗的感觉运动受体。全细胞电流和钙绿1荧光的同时记录显示[Ca(2 +)](i)增加了两个分量。 Ca(2+)通过顶部膜的初始进入后,第二个和更大的肌醇三磷酸(InsP(3))门控的[Ca(2 +)](i)激增发生在发束的底部。该细胞内Ca(2+)释放部位的电子显微镜表明,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InsP(3)受体共享此位置。与链接到ATP-P2受体的Ca(2+)动员的第二信使系统一致,我们还确定了立体感中存在G蛋白的同种型。电压驱动细胞形状变化和非线性电容的ATP之前和之后进行了监测,表明ATP诱发的[Ca(2 +)](i)的上升不会干扰OHC电动力机制。第二个信使信号传导机制绕过了纤毛虫的Ca(2+)清除能力,并在发束的底部暂时升高了[Ca(2 +)](i),在那里它可以调节非常规肌球蛋白同工酶的作用。参与维持发束的完整性并可能影响机械传导。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号