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小鼠脑室内室管膜纤毛的高速数字成像

High-speed digital imaging of ependymal cilia in the murine brain.

作者信息

Lechtreck Karl-Ferdinand, Sanderson Michael J, Witman George B

机构信息

Department of Cell Biology, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA.

出版信息

Methods Cell Biol. 2009;91:255-64. doi: 10.1016/S0091-679X(08)91013-X. Epub 2009 Dec 1.

Abstract

The development and health of mammals requires proper ciliary motility. Ciliated epithelia are found in the airways, the uterus and Fallopian tubes, the efferent ducts of the testes, and the ventricular system of the brain. A technique is described for the motion analysis of ependymal cilia in the murine brain. Vibratome sections of the brain are imaged by differential interference contrast microscopy and recorded by high-speed digital imaging. Side views of individual cilia are traced to establish their bending pattern. Tracking of individual cilia recorded in top view allows determination of bend planarity and beat direction. Ciliary beat frequency is determined from line scans of image sequences. The capacity of the epithelium to move fluid and objects is revealed by analyzing the velocity of polystyrene beads added to brain sections. The technique is useful for detailed assessment of how various conditions or mutations affect the fidelity of ciliary motility at the ependyma. The methods are also applicable to other ciliated epithelia, for example, in airways.

摘要

哺乳动物的发育与健康需要适当的纤毛运动。纤毛上皮存在于气道、子宫和输卵管、睾丸输出小管以及脑室内系统中。本文描述了一种用于小鼠脑室内室管膜纤毛运动分析的技术。通过微分干涉对比显微镜对脑振动切片进行成像,并通过高速数字成像进行记录。追踪单个纤毛的侧视图以确定其弯曲模式。追踪顶视图中记录的单个纤毛可确定弯曲平面度和摆动方向。通过对图像序列进行线扫描来确定纤毛摆动频率。通过分析添加到脑切片中的聚苯乙烯珠的速度,可揭示上皮细胞移动液体和物体的能力。该技术有助于详细评估各种条件或突变如何影响室管膜处纤毛运动的保真度。这些方法也适用于其他纤毛上皮,例如气道中的纤毛上皮。

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