Scheffer Déborah I, Zhang Duan-Sun, Shen Jun, Indzhykulian Artur, Karavitaki K Domenica, Xu Yichao Joy, Wang Qinchuan, Lin Jim Jung-Ching, Chen Zheng-Yi, Corey David P
Howard Hughes Medical Institute and Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA; Department of Otology and Laryngology, Massachusetts Eye and Ear and Harvard Medical School, Boston, MA 02114, USA.
Howard Hughes Medical Institute and Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Cell Rep. 2015 Mar 24;10(11):1811-8. doi: 10.1016/j.celrep.2015.02.042. Epub 2015 Mar 12.
Hair cells of the inner ear are mechanoreceptors for hearing and balance, and proteins highly enriched in hair cells may have specific roles in the development and maintenance of the mechanotransduction apparatus. We identified XIRP2/mXinβ as an enriched protein likely to be essential for hair cells. We found that different isoforms of this protein are expressed and differentially located: short splice forms (also called XEPLIN) are targeted more to stereocilia, whereas two long isoforms containing a XIN-repeat domain are in both stereocilia and cuticular plates. Mice lacking the Xirp2 gene developed normal stereocilia bundles, but these degenerated with time: stereocilia were lost and long membranous protrusions emanated from the nearby apical surfaces. At an ultrastructural level, the paracrystalline actin filaments became disorganized. XIRP2 is apparently involved in the maintenance of actin structures in stereocilia and cuticular plates of hair cells, and perhaps in other organs where it is expressed.
内耳的毛细胞是听觉和平衡的机械感受器,毛细胞中高度富集的蛋白质可能在机械转导装置的发育和维持中具有特定作用。我们鉴定出XIRP2/mXinβ是一种可能对毛细胞至关重要的富集蛋白。我们发现该蛋白的不同异构体表达且定位不同:短剪接形式(也称为XEPLIN)更多地靶向静纤毛,而含有XIN重复结构域的两种长异构体则存在于静纤毛和角质板中。缺乏Xirp2基因的小鼠发育出正常的静纤毛束,但这些静纤毛束会随着时间退化:静纤毛丢失,附近顶端表面出现长的膜状突起。在超微结构水平上,平行排列的肌动蛋白丝变得紊乱。XIRP2显然参与维持毛细胞静纤毛和角质板中的肌动蛋白结构,也许还参与其表达的其他器官中的相关过程。