Abstract

Hair cells (HCs) in the mammalian cochleae cannot spontaneously regenerate once damaged, resulting in permanent hearing loss. It has been shown that Atoh1 overexpression induces hair cell-like cells (HCLCs) in the cochlea of newborn rodents, but this is hard to achieve in adult mammals. In this study, we used a three-dimensional cochlear culture system and an adenoviral-mediated delivery vector to overexpress Atoh1 in adult mouse cochleae. HCLCs were successfully induced from 3 days after virus infection (3 DVI) in vitro, and the number increased with time. HCLCs were myosin7a positive and distinguishable from remnant HCs in a culture environment. Meanwhile, patch-clamp results showed that noninactive outward potassium currents (sustained outward potassium currents) could be recorded in HCLCs and that their magnitude increased with time, similar to normal HCs. Furthermore, transient HCN currents were recorded in some HCLCs, indicating that the HCLCs experienced a developmental stage similar to normal HCs. We also compared the electrophysiological features of HCLCs from adult mice with native HCs and found the HCLCs gradually matured, similar to the normal HCs. Meanwhile, HCLCs from adult mice possessed the same bundles as developmental HCs. However, these HCLCs did not express prestin, which is a special marker for outer hair cells (OHCs), even at 13 DVI. These results demonstrate that Atoh1 overexpression induces HCLC formation in the adult mammalian cochlea and that these HCLCs were functional and experienced a developmental process similar to that of normal HCs.

Highlights

  • Hair cells (HCs), which serve as inner ear sensory cells, are essential for the transduction of mechanical stimulation into hearing and balance signals in the inner ear

  • hair cell-like cells (HCLCs) were distinguishable from the remnant native HCs

  • HCLCs were induced in adult mouse cochleae by Atoh1 overexpression, and they were distinguishable in the sensory region

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Summary

Introduction

Hair cells (HCs), which serve as inner ear sensory cells, are essential for the transduction of mechanical stimulation into hearing and balance signals in the inner ear. In lower vertebrates, such as birds and zebrafish, lost HCs can be replaced by spontaneous HC regeneration [1,2,3,4]. Atoh is gradually upregulated before HC formation and is downregulated during the HC maturation process [17,18,19]. Atoh overexpression induces the formation of Neural Plasticity

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