Orly Gilad, Manor Uri, Gov Nir S
Department of Chemical Physics, The Weizmann Institute of Science, P.O.B. 26, Rehovot, Israel 76100.
Section on Organelle Biology, 35 Convent Drive, Porter Neuroscience II, NIH, Bethesda, Md. 20892, United States.
PLoS One. 2015 Jul 24;10(7):e0127926. doi: 10.1371/journal.pone.0127926. eCollection 2015.
Cochlear hair cell bundles, made up of 10s to 100s of individual stereocilia, are essential for hearing, and even relatively minor structural changes, due to mutations or injuries, can result in total deafness. Consistent with its specialized role, the staircase geometry (SCG) of hair cell bundles presents one of the most striking, intricate, and precise organizations of actin-based cellular shapes. Composed of rows of actin-filled stereocilia with increasing lengths, the hair cell's staircase-shaped bundle is formed from a progenitor field of smaller, thinner, and uniformly spaced microvilli with relatively invariant lengths. While recent genetic studies have provided a significant increase in information on the multitude of stereocilia protein components, there is currently no model that integrates the basic physical forces and biochemical processes necessary to explain the emergence of the SCG. We propose such a model derived from the biophysical and biochemical characteristics of actin-based protrusions. We demonstrate that polarization of the cell's apical surface, due to the lateral polarization of the entire epithelial layer, plays a key role in promoting SCG formation. Furthermore, our model explains many distinct features of the manifestations of SCG in different species and in the presence of various deafness-associated mutations.
耳蜗毛细胞束由数十到数百根单独的静纤毛组成,对听力至关重要,即使是由于突变或损伤导致的相对较小的结构变化,也可能导致完全失聪。与其特殊作用相一致,毛细胞束的阶梯状几何结构(SCG)呈现出基于肌动蛋白的细胞形状中最显著、最复杂和最精确的组织之一。毛细胞的阶梯状束由一排排长度不断增加的充满肌动蛋白的静纤毛组成,它由一个较小、较细且长度相对不变、间距均匀的微绒毛祖细胞场形成。虽然最近的遗传学研究大大增加了关于众多静纤毛蛋白成分的信息,但目前还没有一个模型能够整合解释SCG出现所需的基本物理力和生化过程。我们提出了一个基于肌动蛋白突起的生物物理和生化特性的模型。我们证明,由于整个上皮层的侧向极化导致细胞顶端表面的极化,在促进SCG形成中起关键作用。此外,我们的模型解释了不同物种以及存在各种与耳聋相关突变时SCG表现的许多独特特征。