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毛细胞静纤毛中游离钙离子浓度的调节

Regulation of free Ca2+ concentration in hair-cell stereocilia.

作者信息

Lumpkin E A, Hudspeth A J

机构信息

Howard Hughes Medical Institute and Laboratory of Sensory Neuroscience, The Rockefeller University, New York, New York 10021-6399, USA.

出版信息

J Neurosci. 1998 Aug 15;18(16):6300-18. doi: 10.1523/JNEUROSCI.18-16-06300.1998.

Abstract

By affecting the activity of the adaptation motor, Ca2+ entering a hair bundle through mechanoelectrical transduction channels regulates the sensitivity of the bundle to stimulation. For adaptation to set the position of mechanosensitivity of the bundle accurately, the free Ca2+ concentration in stereocilia must be tightly controlled. To define the roles of Ca2+-regulatory mechanisms and thus the factors influencing adaptation motor activity, we used confocal microscopy to detect Ca2+ entry into and clearance from individual stereocilia of hair cells dialyzed with the Ca2+ indicator fluo-3. We also developed a model of stereociliary Ca2+ homeostasis that incorporates four regulatory mechanisms: Ca2+ clearance from the bundle by free diffusion in one dimension, Ca2+ extrusion by pumps, Ca2+ binding to fixed stereociliary buffers, and Ca2+ binding to mobile buffers. To test the success of the model, we compared the predicted profiles of fluo-3 fluorescence during the response to mechanical stimulation with the fluorescence patterns measured in individual stereocilia. The results indicate that all four of the Ca2+ regulatory mechanisms must be included in the model to account for the observed rate of clearance of the ion from the hair bundle. The best fit of the model suggests that a free Ca2+ concentration of a few micromolar is attained near the adaptation motor after transduction-channel opening. The free Ca2+ concentration substantially rises only in the upper portion of the stereocilium and quickly falls toward the resting level as adaptation proceeds.

摘要

通过影响适应性运动的活性,经机械电转导通道进入毛束的Ca2+调节毛束对刺激的敏感性。为了使适应性精确设定毛束机械敏感性的位置,必须严格控制静纤毛中游离Ca2+的浓度。为了确定Ca2+调节机制的作用以及影响适应性运动活性的因素,我们使用共聚焦显微镜检测Ca2+进入用Ca2+指示剂fluo-3透析的毛细胞单个静纤毛并从其中清除的情况。我们还建立了一个静纤毛Ca2+稳态模型,该模型纳入了四种调节机制:通过一维自由扩散从毛束清除Ca2+、通过泵排出Ca2+、Ca2+与固定的静纤毛缓冲剂结合以及Ca2+与移动缓冲剂结合。为了检验模型的成功与否,我们将对机械刺激的反应过程中预测的fluo-3荧光图谱与在单个静纤毛中测量的荧光模式进行了比较。结果表明,模型中必须包含所有四种Ca2+调节机制,才能解释从毛束中观察到的离子清除速率。模型的最佳拟合表明,转导通道开放后,在适应性运动附近达到几微摩尔的游离Ca2+浓度。游离Ca2+浓度仅在静纤毛的上部显著升高,并随着适应性过程迅速降至静息水平。

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