Distinct roles of Eps8 in the maturation of cochlear and vestibular hair cells. (22nd July 2016)

• Record Type: Journal Article
• Authors: Tavazzani, Elisa; Spaiardi, Paolo; Zampini, Valeria; Contini, Donatella; Manca, Marco; Russo, Giancarlo; Prigioni, Ivo; Marcotti, Walter; Masetto, Sergio
• Is Part Of: Neuroscience. Volume 328(2016)
• Page Start: 80
• Page End: 91
• Publication Date: 2016-07-22
• Subjects: AP action potential -- d.c. direct current -- EGTA ethylene glycol tetraacetic acid -- Eps8 Epidermal growth factor receptor pathway substrate 8 -- HEPES 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid -- IHCs inner hair cells -- KO knockout -- OHCs outer hair cells -- P postnatal day -- Rm cell membrane input resistance -- Rs series resistance -- RT room temperature -- Vm voltage membrane potential -- Vrest resting membrane potential -- WT wild type; Eps8 -- hair cell -- vestibular -- K+ channel -- hair bundle -- deafness; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2016.04.038
• Languages: English
• ISSNs: 0306-4522

Abstract

Graphical abstract: Highlights: Eps8 is required for proper stereocilia elongation in cochlear and vestibular hair cells. Eps8 -KO vestibular hair cells, unlike cochlear inner hair cells, express their normal pattern of basolateral ion channels. Eps8 deletion similarly affects cochlear and vestibular hair bundles growth but impairs hearing only. Abstract: Several genetic mutations affecting the development and function of mammalian hair cells have been shown to cause deafness but not vestibular defects, most likely because vestibular deficits are sometimes centrally compensated. The study of hair cell physiology is thus a powerful direct approach to ascertain the functional status of the vestibular end organs. Deletion of Epidermal growth factor receptor pathway substrate 8 ( Eps8 ), a gene involved in actin remodeling, has been shown to cause deafness in mice. While both inner and outer hair cells from Eps8 knockout (KO) mice showed abnormally short stereocilia, inner hair cells (IHCs) also failed to acquire mature-type ion channels. Despite the fact that Eps8 is also expressed in vestibular hair cells, Eps8 KO mice show no vestibular deficits. In the present study we have investigated the properties of vestibular Type I and Type II hair cells in Eps8 -KO mice and compared them to those of cochlear IHCs. In the absence of Eps8, vestibular hair cells show normally long kinocilia, significantly shorter stereocilia and a normal pattern of basolateral voltage-dependent ion channels. We have also found that while vestibular hair cells from Eps8 KO mice show normal voltage responses to injected sinusoidal currents, which were used to mimic the mechanoelectrical transducer current, IHCs lose their ability to synchronize their responses to the stimulus. We conclude that the absence of Eps8 produces a weaker phenotype in vestibular hair cells compared to cochlear IHCs, since it affects the hair bundle morphology but not the basolateral membrane currents. This difference is likely to explain the absence of obvious vestibular dysfunction in Eps8 KO mice.