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鸟类耳蜗的肌动蛋白丝、静纤毛和毛细胞。VI. 静纤毛的数量和排列是如何确定的。

Actin filaments, stereocilia and hair cells of the bird cochlea. VI. How the number and arrangement of stereocilia are determined.

作者信息

Tilney L G, Cotanche D A, Tilney M S

机构信息

Department of Biology, University of Pennsylvania, Philadelphia 19104.

出版信息

Development. 1992 Sep;116(1):213-26. doi: 10.1242/dev.116.1.213.

Abstract

Beginning in 8-day embryos, stereocilia sprout from the apical surface of hair cells apparently at random. As the embryo continues to develop, the number of stereocilia increases. By 10 1/2 days the number is approximately the same as that encountered extending from mature hair cells at the same relative positions in the adult cochlea. Surprisingly, over the next 2-3 days the number of stereocilia continues to increase so that hair cells in a 12-day embryo have 1 1/2 to 2 times as many stereocilia as in adult hair cells. In short, there is an overshoot in stereociliary number. During the same period in which stereocilia are formed (9-12 days) the apical surface of each hair cell is filled with closely packed stereocilia; thus the surface area is proportional to the number of stereocilia present per hair cell, as if these features were coupled. The staircase begins to form in a 10-day embryo, with what will be the tallest row beginning to elongate first and gradually row after row begins to elongate by incorporation of stereocilia at the foot of the staircase. Extracellular connections or tip linkages appear as the stereocilia become incorporated into the staircase. After a diminutive staircase has formed, eg. in a 12-day embryo, the remaining stereocilia located at the foot of the staircase begin to be reabsorbed, a process that occurs during the next few days. We conclude that the hair cell determines the number of stereocilia to form by filling up the available apical surface area with stereocilia and then, by cropping back those that are not stabilized by extracellular linkages, arrives at the appropriate number. Furthermore, the stereociliary pattern, which changes from having a round cross-sectional profile to a rectangular one, is generated by these same linkages which lock the stereocilia into a precise pattern. As this pattern is established, we envision that the stereocilia flow over the apical surface until frozen in place by the formation of the cuticular plate in the apical cell cytoplasm.

摘要

从8天龄的胚胎开始,静纤毛显然是随机地从毛细胞的顶端表面长出。随着胚胎继续发育,静纤毛的数量增加。到10.5天时,其数量与成年耳蜗中相同相对位置的成熟毛细胞伸出的静纤毛数量大致相同。令人惊讶的是,在接下来的2 - 3天里,静纤毛的数量继续增加,以至于12天龄胚胎中的毛细胞具有的静纤毛数量是成年毛细胞的1.5至2倍。简而言之,静纤毛数量出现了超调。在静纤毛形成的同一时期(9 - 12天),每个毛细胞的顶端表面布满了紧密排列的静纤毛;因此,表面积与每个毛细胞中存在的静纤毛数量成正比,就好像这些特征是相互关联的。阶梯状结构在10天龄的胚胎中开始形成,将成为最高一排的静纤毛首先开始伸长,然后一排接一排地逐渐通过在阶梯底部并入静纤毛而开始伸长。随着静纤毛并入阶梯状结构,细胞外连接或顶端连接出现。在一个小型的阶梯状结构形成后,例如在12天龄的胚胎中,位于阶梯底部的其余静纤毛开始被重新吸收,这个过程在接下来的几天内发生。我们得出结论,毛细胞通过用静纤毛填满可用的顶端表面积来确定要形成的静纤毛数量,然后,通过修剪那些未被细胞外连接稳定的静纤毛,达到合适的数量。此外,静纤毛的模式从圆形横截面轮廓变为矩形,是由这些将静纤毛锁定成精确模式的相同连接产生的。随着这种模式的建立,我们设想静纤毛在顶端表面流动,直到通过顶端细胞质中角质板的形成而固定到位。

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