Tilney L G, Tilney M S
Hear Res. 1986;22:55-77. doi: 10.1016/0378-5955(86)90077-8.
Within each stereocilium of chick hair cells is a hexagonally packed bundle of actin filaments. Diffraction patterns of thin sections of these bundles reveal that the actin filaments are aligned such that the crossover points of adjacent filaments are in transverse register. Since each actin filament is composed of subunits that are organized in a helical pattern, yet all the actin filaments are in transverse register, crossbridges between filaments can form only at positions dictated by the geometry of the actin helix or at 125 A intervals. Thus the crossbridges appear in electron micrographs as regularly spaced bands (125 A) that are perpendicular to the axis of the stereocilium. From examination of stereocilia of organisms who have a temporary threshold shift due to exposure to loud noise, we know that the integrity of the actin filaments and their crossbridges is essential for hair cell function. However, particularly interesting is that when a stereocilium is bent or displaced, as might occur during stimulation by sound, the actin filaments are not compressed or stretched, but slide past one another so that the bridges become tilted relative to the long axis of the actin filament bundle. Thus, resistance to bending or displacement must be a property of the number of bridges present which in turn is a function of the number and lengths of actin filaments present. Since hair cells in different parts of the cochlea have stereocilia of different, yet predictable lengths and widths, this means that the force needed to displace the stereocilia of hair cells located at different regions of the cochlea will not be the same. This suggests that fine tuning of the hair cells must be a built-in property of the stereocilia. To try to understand how hair cells control the length and number of actin filaments per stereocilium and thus the length and width of the stereocilia, we examined cochlea in chick embryos of increasing maturity. Of interest is that very early in development (10-day embryos) the total hair cell number and position is specified. Thus it is possible to study the growth of stereocilia in cells whose final stereociliary length and width is already known. Stereocilia first elongate (from 8 to 11 days--first phase); they then stop elongating and increase in width (12-16 days--second phase), then elongate again (third phase) to the length appropriate to the position of the hair cell on the cochlea. During the first phase a few actin filaments are present, but initially poorly ordered.(ABSTRACT TRUNCATED AT 400 WORDS)
在鸡毛细胞的每个静纤毛内,是一束呈六边形排列的肌动蛋白丝。这些肌动蛋白丝束的薄切片衍射图样显示,肌动蛋白丝排列整齐,相邻丝的交叉点处于横向对齐状态。由于每条肌动蛋白丝由以螺旋模式排列的亚基组成,而所有肌动蛋白丝都横向对齐,丝之间的横桥只能在由肌动蛋白螺旋几何结构决定的位置或以125埃的间隔形成。因此,在电子显微镜照片中,横桥呈现为垂直于静纤毛轴的规则间隔带(125埃)。通过检查因暴露于高强度噪声而出现暂时阈移的生物体的静纤毛,我们知道肌动蛋白丝及其横桥的完整性对毛细胞功能至关重要。然而,特别有趣的是,当静纤毛弯曲或移位时,比如在声音刺激过程中可能发生的那样,肌动蛋白丝不会被压缩或拉伸,而是相互滑过,这样桥相对于肌动蛋白丝束的长轴就会倾斜。因此,对弯曲或移位的抵抗力必定是现有桥数量的一种特性,而这反过来又是现有肌动蛋白丝数量和长度的函数。由于耳蜗不同部位的毛细胞具有不同但可预测长度和宽度的静纤毛,这意味着使位于耳蜗不同区域的毛细胞静纤毛移位所需的力是不一样的。这表明毛细胞的精细调节必定是静纤毛的一种固有特性。为了试图理解毛细胞如何控制每个静纤毛中肌动蛋白丝的长度和数量,从而控制静纤毛的长度和宽度,我们检查了发育成熟度不断增加的鸡胚的耳蜗。有趣的是,在发育早期(10日龄胚胎),毛细胞的总数和位置就已确定。因此,有可能研究那些最终静纤毛长度和宽度已知的细胞中静纤毛的生长情况。静纤毛首先伸长(8至11天——第一阶段);然后停止伸长并增宽(12至16天——第二阶段),接着再次伸长(第三阶段)至与耳蜗上毛细胞位置相适应的长度。在第一阶段,存在一些肌动蛋白丝,但最初排列不佳。(摘要截选至400字)