Abstract

Control of the extracellular environment of inner ear hair cells by ionic transporters is crucial for hair cell function. In addition to inner ear hair cells, aquatic vertebrates have hair cells on the surface of their body in the lateral line system. The ionic environment of these cells also appears to be regulated, although the mechanisms of this regulation are less understood than those of the mammalian inner ear. We identified the merovingian mutant through genetic screening in zebrafish for genes involved in drug-induced hair cell death. Mutants show complete resistance to neomycin-induced hair cell death and partial resistance to cisplatin-induced hair cell death. This resistance is probably due to impaired drug uptake as a result of reduced mechanotransduction ability, suggesting that the mutants have defects in hair cell function independent of drug treatment. Through genetic mapping we found that merovingian mutants contain a mutation in the transcription factor gcm2. This gene is important for the production of ionocytes, which are cells crucial for whole body pH regulation in fish. We found that merovingian mutants showed an acidified extracellular environment in the vicinity of both inner ear and lateral line hair cells. We believe that this acidified extracellular environment is responsible for the defects seen in hair cells of merovingian mutants, and that these mutants would serve as a valuable model for further study of the role of pH in hair cell function.

Highlights

  • Hearing loss is currently the most prevalent sensory disorder; about 10% of adults and 35% of people over 65 suffer from hearing impairment (Davis, 1989; Ries, 1994)

  • This resistance appears to be due to impaired mechanotransduction ability as the merovingian mutants show audiovestibular behavioral defects. gcm2 is important for the production of ionocytes, cells that are crucial for whole body pH regulation in fish, and the merovingian mutants show acidification of the extracellular environment throughout their body

  • This study and conclusion are supported by the presence of sensorineural hearing loss in distal renal tubular acidosis, a disorder that is caused by mutations in the pH-regulating H+-ATPase complex, they support a role for pH regulation in normal hair cell function

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Summary

Introduction

Hearing loss is currently the most prevalent sensory disorder; about 10% of adults and 35% of people over 65 suffer from hearing impairment (Davis, 1989; Ries, 1994). The inner ear is highly sensitive to damage, and numerous genetic mutations and environmental insults lead to hearing loss (Dror and Avraham, 2009; Rybak and Ramkumar, 2007; Sliwinska-Kowalska and Davis, 2012). The inner ear is enriched in ionic transporters highly expressed in the kidney, such as the H+-ATPases and Cl–/HCO3– exchangers (Lang et al, 2007), suggesting a role for ionic homeostasis in the functioning of the audiovestibular system. Mutations in H+-ATPase transporter subunits cause hearing loss in the human disease distal rental tubular acidosis (dRTA) and in mouse models of this disease (Hennings et al, 2012; Karet et al, 1999; Norgett et al, 2012; Smith et al, 2000)

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