Department of Biology, Indiana University-Purdue University Indianapolis, 723 West Michigan Street, Indianapolis, IN 46202, USA.
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH, 35A Convent Drive, Bethesda, MD 20892, USA.
Curr Biol. 2021 Mar 22;31(6):1141-1153.e7. doi: 10.1016/j.cub.2020.12.006. Epub 2021 Jan 4.
Stereocilia on auditory sensory cells are actin-based protrusions that mechanotransduce sound into an electrical signal. These stereocilia are arranged into a bundle with three rows of increasing length to form a staircase-like morphology that is required for hearing. Stereocilia in the shorter rows, but not the tallest row, are mechanotransducing because they have force-sensitive channels localized at their tips. The onset of mechanotransduction during mouse postnatal development refines stereocilia length and width. However, it is unclear how actin is differentially regulated between stereocilia in the tallest row of the bundle and the shorter, mechanotransducing rows. Here, we show actin turnover is increased at the tips of mechanotransducing stereocilia during bundle maturation. Correspondingly, from birth to postnatal day 6, these stereocilia had increasing amounts of available actin barbed ends, where monomers can be added or lost readily, as compared with the non-mechanotransducing stereocilia in the tallest row. The increase in available barbed ends depended on both mechanotransduction and MYO15 or EPS8, which are required for the normal specification and elongation of the tallest row of stereocilia. We also found that loss of the F-actin-severing proteins ADF and cofilin-1 decreased barbed end availability at stereocilia tips. These proteins enriched at mechanotransducing stereocilia tips, and their localization was perturbed by the loss of mechanotransduction, MYO15, or EPS8. Finally, stereocilia lengths and widths were dysregulated in Adf and Cfl1 mutants. Together, these data show that actin is remodeled, likely by a severing mechanism, in response to mechanotransduction.
听觉感觉细胞上的纤毛是基于肌动蛋白的突起,将声音机械转化为电信号。这些纤毛排列成一束,有三排,长度逐渐增加,形成类似于楼梯的形态,这是听觉所必需的。较短排的纤毛(但不是最高排的纤毛)具有机械转导功能,因为它们的尖端有受力敏感的通道。在小鼠出生后的发育过程中,机械转导的开始会使纤毛的长度和宽度得到精细调整。然而,目前尚不清楚束状中最高排的纤毛和较短的机械转导排的纤毛之间肌动蛋白是如何被差异化调节的。在这里,我们发现在束状成熟过程中,机械转导纤毛的尖端肌动蛋白周转率增加。相应地,与束状中最高排的非机械转导纤毛相比,从出生到出生后第 6 天,这些纤毛具有越来越多的可用肌动蛋白有丝分裂末端,其中单体可以容易地添加或丢失。可用的有丝分裂末端的增加取决于机械转导以及 MYO15 或 EPS8,这两者对于最高排纤毛的正常形成和伸长都是必需的。我们还发现,F-肌动蛋白切割蛋白 ADF 和肌动蛋白结合蛋白 1 的缺失会降低纤毛尖端的有丝分裂末端可用性。这些蛋白质在机械转导纤毛尖端富集,其定位因机械转导、MYO15 或 EPS8 的缺失而受到干扰。最后,Adf 和 Cfl1 突变体中的纤毛长度和宽度失调。总之,这些数据表明,肌动蛋白通过一种切割机制进行重塑,以响应机械转导。