4.8 Article

A critical period of prehearing spontaneous Ca2+ spiking is required for hair-bundle maintenance in inner hair cells

期刊

EMBO JOURNAL
卷 42, 期 4, 页码 -

出版社

WILEY
DOI: 10.15252/embj.2022112118

关键词

calcium waves; development; hair cell; mechanoelectrical transduction; spontaneous action potentials

向作者/读者索取更多资源

Sensory-independent Ca2+ spiking regulates the development of mammalian sensory systems. In immature cochlea, inner hair cells (IHCs) generate spontaneous Ca2+ action potentials (APs) either intrinsically or through intercellular Ca2+ waves. This study finds that intrinsic Ca2+ APs in IHCs, but not those induced by Ca2+ waves, play a role in the maturation and maintenance of hair bundles. By overexpressing the Kir2.1 potassium channel in IHCs, the study shows that absence of intrinsic Ca2+ APs leads to loss of mechanoelectrical transduction and upregulation of certain pathways related to morphogenesis and signaling in the Kir2.1-OE mice.
Sensory-independent Ca2+ spiking regulates the development of mammalian sensory systems. In the immature cochlea, inner hair cells (IHCs) fire spontaneous Ca2+ action potentials (APs) that are generated either intrinsically or by intercellular Ca2+ waves in the nonsensory cells. The extent to which either or both of these Ca2+ signalling mechansims are required for IHC maturation is unknown. We find that intrinsic Ca2+ APs in IHCs, but not those elicited by Ca2+ waves, regulate the maturation and maintenance of the stereociliary hair bundles. Using a mouse model in which the potassium channel Kir2.1 is reversibly overexpressed in IHCs (Kir2.1-OE), we find that IHC membrane hyperpolarization prevents IHCs from generating intrinsic Ca2+ APs but not APs induced by Ca2+ waves. Absence of intrinsic Ca2+ APs leads to the loss of mechanoelectrical transduction in IHCs prior to hearing onset due to progressive loss or fusion of stereocilia. RNA-sequencing data show that pathways involved in morphogenesis, actin filament-based processes, and Rho-GTPase signaling are upregulated in Kir2.1-OE mice. By manipulating in vivo expression of Kir2.1 channels, we identify a critical time period during which intrinsic Ca2+ APs in IHCs regulate hair-bundle function.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据