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Erschienen in: Journal of the Association for Research in Otolaryngology 3/2016

15.03.2016 | Research Article

QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice

verfasst von: Kevin K. Ohlemiller, Anna L. Kiener, Patricia M. Gagnon

Erschienen in: Journal of the Association for Research in Otolaryngology | Ausgabe 3/2016

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Abstract

We reported earlier that the endocochlear potential (EP) differs between C57BL/6J (B6) and BALB/cJ (BALB) mice, being lower in BALBs by about 10 mV (Ohlemiller et al. Hear Res 220: 10–26, 2006). This difference corresponds to strain differences with respect to the density of marginal cells in cochlear stria vascularis. After about 1 year of age, BALB mice also tend toward EP reduction that correlates with further marginal cell loss. We therefore suggested that early sub-clinical features of the BALB stria vascularis may predispose these mice to a condition modeling Schuknecht’s strial presbycusis. We further reported (Ohlemiller et al. J Assoc Res Otolaryngol 12: 45–58, 2011) that the acute effects of a 2-h 110 dB SPL noise exposure differ between B6 and BALB mice, such that the EP remains unchanged in B6 mice, but is reduced by 40–50 mV in BALBs. In about 25 % of BALBs, the EP does not completely recover, so that permanent EP reduction may contribute to noise-induced permanent threshold shifts in BALBs. To identify genes and alleles that may promote natural EP variation as well as noise-related EP reduction in BALB mice, we have mapped related quantitative trait loci (QTLs) using 12 recombinant inbred (RI) strains formed from B6 and BALB (CxB1–CxB12). EP and strial marginal cell density were measured in B6 mice, BALB mice, their F1 hybrids, and RI mice without noise exposure, and 1–3 h after broadband noise (4–45 kHz, 110 dB SPL, 2 h). For unexposed mice, the strain distribution patterns for EP and marginal cell density were used to generate preliminary QTL maps for both EP and marginal cell density. Six QTL regions were at least statistically suggestive, including a significant QTL for marginal cell density on chromosome 12 that overlapped a weak QTL for EP variation. This region, termed Maced (Marginal cell density QTL) supports the notion of marginal cell density as a genetically influenced contributor to natural EP variation. Candidate genes for Maced notably include Foxg1, Foxa1, Akap6, Nkx2-1, and Pax9. Noise exposure produced significant EP reductions in two RI strains as well as significant EP increases in two RI strains. QTL mapping of the EP in noise-exposed RI mice yielded four suggestive regions. Two of these overlapped with QTL regions we previously identified for noise-related EP reduction in CBA/J mice (Ohlemiller et al. Hear Res 260: 47–53, 2010) on chromosomes 5 and 18 (Nirep). The present map may narrow the Nirep interval to a ~10-Mb region of proximal Chr. 18 that includes Zeb1, Arhgap12, Mpp7, and Gjd4. This study marks the first exploration of natural gene variants that modulate the EP. Their orthologs may underlie some human hearing loss that originates in the lateral wall.
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Literatur
Zurück zum Zitat Abraira VE, Satoh T, Fekete DM, Goodrich LV (2010) Vertebrate Lrig3-ErbB interactions occur in vitro but are unlikely to play a role in Lrig3-dependent inner ear morphogenesis. PLoS One 5, e8981PubMedPubMedCentralCrossRef Abraira VE, Satoh T, Fekete DM, Goodrich LV (2010) Vertebrate Lrig3-ErbB interactions occur in vitro but are unlikely to play a role in Lrig3-dependent inner ear morphogenesis. PLoS One 5, e8981PubMedPubMedCentralCrossRef
Zurück zum Zitat Adams JC (2009) Immunocytochemical traits of type IV fibrocytes and their possible relations to cochlear function and pathology. J Assoc Res Otolaryngol 10:369–382PubMedPubMedCentralCrossRef Adams JC (2009) Immunocytochemical traits of type IV fibrocytes and their possible relations to cochlear function and pathology. J Assoc Res Otolaryngol 10:369–382PubMedPubMedCentralCrossRef
Zurück zum Zitat Ahmad M, Bohne BA, Harding GW (2003) An in vivo tracer study of noise-induced damage to the reticular lamina. Hear Res 175:82–100PubMedCrossRef Ahmad M, Bohne BA, Harding GW (2003) An in vivo tracer study of noise-induced damage to the reticular lamina. Hear Res 175:82–100PubMedCrossRef
Zurück zum Zitat Axelsson A, Lindgren F (1985) Is there a relationship between hypercholesterolemia and noise-induced hearing loss? Acta Otolaryngol 100:379–386PubMedCrossRef Axelsson A, Lindgren F (1985) Is there a relationship between hypercholesterolemia and noise-induced hearing loss? Acta Otolaryngol 100:379–386PubMedCrossRef
Zurück zum Zitat Bahloul A, Simmler M-C, Michel V, Leibovici M, Perfettini I, Roux I, Weil D, Nouaille S, Zuo J, Zadro C, Licastro D, Gasparini P, Avan P, Hardelin J-P, Petit C (2009) Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear cells. EMBO Mol Med 1:125–138PubMedPubMedCentralCrossRef Bahloul A, Simmler M-C, Michel V, Leibovici M, Perfettini I, Roux I, Weil D, Nouaille S, Zuo J, Zadro C, Licastro D, Gasparini P, Avan P, Hardelin J-P, Petit C (2009) Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear cells. EMBO Mol Med 1:125–138PubMedPubMedCentralCrossRef
Zurück zum Zitat Bell D, Streit A, Gorospe I, Varela-Nieto I, Alsina B, Giraldez F (2008) Spatial and temporal segregation of auditory and vestibular neurons in the otic placode. Dev Biol 322:109–120PubMedCrossRef Bell D, Streit A, Gorospe I, Varela-Nieto I, Alsina B, Giraldez F (2008) Spatial and temporal segregation of auditory and vestibular neurons in the otic placode. Dev Biol 322:109–120PubMedCrossRef
Zurück zum Zitat Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, Camper SA, Friedman TB (2003) Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Hum Mol Genet 12:2049–2061PubMedCrossRef Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, Camper SA, Friedman TB (2003) Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Hum Mol Genet 12:2049–2061PubMedCrossRef
Zurück zum Zitat Berndt H, Wagner H (1979) Influence of thyroid state and improved hypoxia tolerance on noise-induced cochlea damage. Eur Arch Otorhinolaryngol 224:125–128CrossRef Berndt H, Wagner H (1979) Influence of thyroid state and improved hypoxia tolerance on noise-induced cochlea damage. Eur Arch Otorhinolaryngol 224:125–128CrossRef
Zurück zum Zitat Bohnenpoll T, Trowe M-O, Wojahn I, Taketo MM, Petry M, Kispert A (2014) Canonical Wnt signaling regulates the proliferative expansion and differentiation of fibrocytes in the murine inner ear. Dev Biol 391:54–65PubMedCrossRef Bohnenpoll T, Trowe M-O, Wojahn I, Taketo MM, Petry M, Kispert A (2014) Canonical Wnt signaling regulates the proliferative expansion and differentiation of fibrocytes in the murine inner ear. Dev Biol 391:54–65PubMedCrossRef
Zurück zum Zitat Braunstein EM, Monks DC, Aggarwal VS, Arnold JS, Morrow BE (2009) Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis. BMC Dev Biol 9:31PubMedPubMedCentralCrossRef Braunstein EM, Monks DC, Aggarwal VS, Arnold JS, Morrow BE (2009) Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis. BMC Dev Biol 9:31PubMedPubMedCentralCrossRef
Zurück zum Zitat Bryda EC, Johnson NT, Ohlemiller KK, Besch-Williford CL, Moore E, Bram RJ (2012) Conditional deletion of calcium-modulating cyclophilin ligand causes deafness in mice. Mamm Genome 23:270–276PubMedCrossRef Bryda EC, Johnson NT, Ohlemiller KK, Besch-Williford CL, Moore E, Bram RJ (2012) Conditional deletion of calcium-modulating cyclophilin ligand causes deafness in mice. Mamm Genome 23:270–276PubMedCrossRef
Zurück zum Zitat Cai Q, Patel M, Coling DE, Hu BH (2012) Transcriptional changes in adhesion-related genes are site-specific during noise-induced cochlear pathogenesis. Neurobiol Dis 45:723–732PubMedPubMedCentralCrossRef Cai Q, Patel M, Coling DE, Hu BH (2012) Transcriptional changes in adhesion-related genes are site-specific during noise-induced cochlear pathogenesis. Neurobiol Dis 45:723–732PubMedPubMedCentralCrossRef
Zurück zum Zitat Chaplin JW, Kasahara S, Clark EA, Ledbetter JA (2009) CD180 is a positive regulator of TLR signals in B cells. J Immunol 182:135–164 Chaplin JW, Kasahara S, Clark EA, Ledbetter JA (2009) CD180 is a positive regulator of TLR signals in B cells. J Immunol 182:135–164
Zurück zum Zitat Conlee JW, Abdul-Baqi KJ, McCandless GA, Creel DJ (1986) Differential susceptibility to noise-induced permanent threshold shift between albino and pigmented guinea pigs. Hear Res 23:81–91PubMedCrossRef Conlee JW, Abdul-Baqi KJ, McCandless GA, Creel DJ (1986) Differential susceptibility to noise-induced permanent threshold shift between albino and pigmented guinea pigs. Hear Res 23:81–91PubMedCrossRef
Zurück zum Zitat Conlee JW, Abdul-Baqi KJ, McCandless GA, Creel DJ (1988) Effects of aging on normal hearing loss and noise-induced threshold shift in albino and pigmented guinea pigs. Acta Otolaryngol 106:64–70PubMedCrossRef Conlee JW, Abdul-Baqi KJ, McCandless GA, Creel DJ (1988) Effects of aging on normal hearing loss and noise-induced threshold shift in albino and pigmented guinea pigs. Acta Otolaryngol 106:64–70PubMedCrossRef
Zurück zum Zitat Crumling MA, Liu L, Thomas PV, Benson J, Kanicki A, Kabara L, Halsey K, Dolan DF, Duncan RK (2012) Hearing loss and hair cell death in mice given the cholesterol-chelating agent hydroxypropyl-beta-cyclodextrin. PLoS One 7:12CrossRef Crumling MA, Liu L, Thomas PV, Benson J, Kanicki A, Kabara L, Halsey K, Dolan DF, Duncan RK (2012) Hearing loss and hair cell death in mice given the cholesterol-chelating agent hydroxypropyl-beta-cyclodextrin. PLoS One 7:12CrossRef
Zurück zum Zitat Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, Smith RJH, Timmermans J-P, Van Camp G (2003) The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. Histochem Cell Biol 119:247–256PubMed Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, Smith RJH, Timmermans J-P, Van Camp G (2003) The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. Histochem Cell Biol 119:247–256PubMed
Zurück zum Zitat Diaz RC, Vazquez AE, Dou H, Wei D, Cardell EL, Lingrel J, Shull GE, Doyle KJ, Yamoah EN (2007) Conservation of hearing by simultaneous mutation of Na, K-ATPase and NKCCl. J Assoc Res Otolaryngol 8:422–434PubMedPubMedCentralCrossRef Diaz RC, Vazquez AE, Dou H, Wei D, Cardell EL, Lingrel J, Shull GE, Doyle KJ, Yamoah EN (2007) Conservation of hearing by simultaneous mutation of Na, K-ATPase and NKCCl. J Assoc Res Otolaryngol 8:422–434PubMedPubMedCentralCrossRef
Zurück zum Zitat Diviani D, Maric D, López IP, Cavin S, del Vescovo CD (2013) A-kinase anchoring proteins: molecular regulators of the cardiac stress response. Biochim Biophys Acta Mol Cell Res 1833:901–908CrossRef Diviani D, Maric D, López IP, Cavin S, del Vescovo CD (2013) A-kinase anchoring proteins: molecular regulators of the cardiac stress response. Biochim Biophys Acta Mol Cell Res 1833:901–908CrossRef
Zurück zum Zitat Dong H, Zhang P, Song I, Petralia RS, Liao D, Huganir RL (1999) Characterization of the glutamate receptor-interacting proteins GRIP1 and GRIP2. J Neurosci Methods 19:6930–6941 Dong H, Zhang P, Song I, Petralia RS, Liao D, Huganir RL (1999) Characterization of the glutamate receptor-interacting proteins GRIP1 and GRIP2. J Neurosci Methods 19:6930–6941
Zurück zum Zitat Dunn KJ, Williams BO, Li Y, Pavan WJ (2000) Neural crest-directed gene transfer demonstrates Wnt1 role in melanocyte expansion and differentiation during mouse development. Proc Natl Acad Sci U S A 97:10050–10055PubMedPubMedCentralCrossRef Dunn KJ, Williams BO, Li Y, Pavan WJ (2000) Neural crest-directed gene transfer demonstrates Wnt1 role in melanocyte expansion and differentiation during mouse development. Proc Natl Acad Sci U S A 97:10050–10055PubMedPubMedCentralCrossRef
Zurück zum Zitat Duvall AJ, Ward WD, Lauhala KE (1974) Stria ultrastructure and vessel transport in acoustic trauma. Ann Otol Rhinol Laryngol 83:498–514PubMed Duvall AJ, Ward WD, Lauhala KE (1974) Stria ultrastructure and vessel transport in acoustic trauma. Ann Otol Rhinol Laryngol 83:498–514PubMed
Zurück zum Zitat Erway LC, Willott JF, Archer JR, Harrison DE (1993) Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains. Hear Res 65:125–132PubMedCrossRef Erway LC, Willott JF, Archer JR, Harrison DE (1993) Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains. Hear Res 65:125–132PubMedCrossRef
Zurück zum Zitat Fujinami Y, Mutai H, Kamiya K, Mizutari K, Fujii M, Matsunaga T (2012) Enhanced expression of C/EBP homologous protein (CHOP) precedes degeneration of fibrocytes in the lateral wall after acute cochlear mitochondrial dysfunction induced by 3-nitropropionic acid. Neurochem Int 56:487–494CrossRef Fujinami Y, Mutai H, Kamiya K, Mizutari K, Fujii M, Matsunaga T (2012) Enhanced expression of C/EBP homologous protein (CHOP) precedes degeneration of fibrocytes in the lateral wall after acute cochlear mitochondrial dysfunction induced by 3-nitropropionic acid. Neurochem Int 56:487–494CrossRef
Zurück zum Zitat Furukawa Y, Kawasoe T, Daigo Y, Nishiwaki T, Ishiguro H, Takahashi M, Kitayama J, Nakamura Y (2001) Isolation of a novel human gene, ARHGAP9 encoding a Rho-GTPase activating protein. Biochem Biophys Res Commun 284:643–649PubMedCrossRef Furukawa Y, Kawasoe T, Daigo Y, Nishiwaki T, Ishiguro H, Takahashi M, Kitayama J, Nakamura Y (2001) Isolation of a novel human gene, ARHGAP9 encoding a Rho-GTPase activating protein. Biochem Biophys Res Commun 284:643–649PubMedCrossRef
Zurück zum Zitat Garland P, Quraishe S, French P, O'Connor V (2008) Expression of the MAST family of serine/threonine kinases. Brain Res Rev 1195:12–19CrossRef Garland P, Quraishe S, French P, O'Connor V (2008) Expression of the MAST family of serine/threonine kinases. Brain Res Rev 1195:12–19CrossRef
Zurück zum Zitat Gratton MA, Eleftheriadou A, Garcia J, Verduzco E, Martin GK, Lonsbury–Martin BL, Vázquez AE (2011) Noise-induced changes in gene expression in the cochleae of mice differing in their susceptibility to noise damage. Hear Res 2011:211–226CrossRef Gratton MA, Eleftheriadou A, Garcia J, Verduzco E, Martin GK, Lonsbury–Martin BL, Vázquez AE (2011) Noise-induced changes in gene expression in the cochleae of mice differing in their susceptibility to noise damage. Hear Res 2011:211–226CrossRef
Zurück zum Zitat Han F, Zhang H, Gu L (2005) Expression and its significance of aquaporins in normal guinea pig inner ears. J Clin Otorhinolaryngol 19:10 Han F, Zhang H, Gu L (2005) Expression and its significance of aquaporins in normal guinea pig inner ears. J Clin Otorhinolaryngol 19:10
Zurück zum Zitat Hao X, Xing Y, Moore MW, Zhang J, Han D, Schulte BA, Dubno JR, Lang H (2014) Sox10 expressing cells in the lateral wall of the aged mouse and human cochlea. PLoS One 9, e97389PubMedPubMedCentralCrossRef Hao X, Xing Y, Moore MW, Zhang J, Han D, Schulte BA, Dubno JR, Lang H (2014) Sox10 expressing cells in the lateral wall of the aged mouse and human cochlea. PLoS One 9, e97389PubMedPubMedCentralCrossRef
Zurück zum Zitat Hertzano R, Elkon R, Kurima K, Morrisson A, Chan S-L, Sallin M, Biedlingmaier A, Darling DS, Griffith AJ, Eisenman DJ, Strome SE (2011) Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis. PLoS One 7, e1002309 Hertzano R, Elkon R, Kurima K, Morrisson A, Chan S-L, Sallin M, Biedlingmaier A, Darling DS, Griffith AJ, Eisenman DJ, Strome SE (2011) Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis. PLoS One 7, e1002309
Zurück zum Zitat Hibino H, Nin F, Tsuzuki C, Kurachi Y (2010) How is the highly positive endocochlear potential formed? The specific architecture of the stria vascularis and the roles of the ion-transport apparatus. Pflugers Arch Eur J Physiol 459:521–533CrossRef Hibino H, Nin F, Tsuzuki C, Kurachi Y (2010) How is the highly positive endocochlear potential formed? The specific architecture of the stria vascularis and the roles of the ion-transport apparatus. Pflugers Arch Eur J Physiol 459:521–533CrossRef
Zurück zum Zitat Hirose K, Liberman MC (2003) Lateral wall histopathology and endocochlear potential in the noise-damaged mouse cochlea. J Assoc Res Otolaryngol 4:339–352PubMedPubMedCentralCrossRef Hirose K, Liberman MC (2003) Lateral wall histopathology and endocochlear potential in the noise-damaged mouse cochlea. J Assoc Res Otolaryngol 4:339–352PubMedPubMedCentralCrossRef
Zurück zum Zitat Hitzemann R, Bell J, Rasmussen E, McCaughran J (2001) Chapter 21. Mapping the genes for the acoustic startle response (ASR) and prepulse inhibition of the ASR in the BxD recombinant inbred series: Effect of high-frequency hearing loss and cochlear pathology. In: Willott JF (ed) Handbook of mouse auditory research: from behavior to molecular biology. CRC Press, Boca Raton, pp 441–455 Hitzemann R, Bell J, Rasmussen E, McCaughran J (2001) Chapter 21. Mapping the genes for the acoustic startle response (ASR) and prepulse inhibition of the ASR in the BxD recombinant inbred series: Effect of high-frequency hearing loss and cochlear pathology. In: Willott JF (ed) Handbook of mouse auditory research: from behavior to molecular biology. CRC Press, Boca Raton, pp 441–455
Zurück zum Zitat Hjeij R, Lindstrand A, Francis R, Zariwala MA, Liu X, Li Y, Damerla R, Dougherty GW, Abouhamed M, Olbrich H, Loges NT, Pennekamp P, Davis EE, Carvalho CMB, Pehlivan D, Werner C, Raidt J, Kohler G, Haffner K, Reyes-Mugica M, Lupski JR, Leigh MW, Rosenfeld M, Morgan LC, Knowles MR, Lo CW, Katsanis N, Omran H (2013) ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. Am J Med Genet 93:357–367 Hjeij R, Lindstrand A, Francis R, Zariwala MA, Liu X, Li Y, Damerla R, Dougherty GW, Abouhamed M, Olbrich H, Loges NT, Pennekamp P, Davis EE, Carvalho CMB, Pehlivan D, Werner C, Raidt J, Kohler G, Haffner K, Reyes-Mugica M, Lupski JR, Leigh MW, Rosenfeld M, Morgan LC, Knowles MR, Lo CW, Katsanis N, Omran H (2013) ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. Am J Med Genet 93:357–367
Zurück zum Zitat Housley GD, Morton-Jones R, Vlajkovic SM, Telang RS, Paramanthasivam V, Tadros SF, Wong ACY, Froud KE, Cederholm JME, Sivakumaran Y, Snguanwongchai P, Khakh BS, Cockayne DA, Thorne PR, Ryan AF (2013) ATP-gated ion channels mediate adaptation to elevated sound levels. Proc Natl Acad Sci U S A 110:7494–7499PubMedPubMedCentralCrossRef Housley GD, Morton-Jones R, Vlajkovic SM, Telang RS, Paramanthasivam V, Tadros SF, Wong ACY, Froud KE, Cederholm JME, Sivakumaran Y, Snguanwongchai P, Khakh BS, Cockayne DA, Thorne PR, Ryan AF (2013) ATP-gated ion channels mediate adaptation to elevated sound levels. Proc Natl Acad Sci U S A 110:7494–7499PubMedPubMedCentralCrossRef
Zurück zum Zitat Howard BA (2012) In the beginning: the establishment of the mammary lineage during embryogenesis. Semim Cell Dev Biol 23:574–582CrossRef Howard BA (2012) In the beginning: the establishment of the mammary lineage during embryogenesis. Semim Cell Dev Biol 23:574–582CrossRef
Zurück zum Zitat Hoya N, Okamoto Y, Kamiya K, Fujii M, Matsunaga T (2004) A novel animal model of acute cochlear mitochondrial dysfunction. Neuroreport 15:1597–1600PubMedCrossRef Hoya N, Okamoto Y, Kamiya K, Fujii M, Matsunaga T (2004) A novel animal model of acute cochlear mitochondrial dysfunction. Neuroreport 15:1597–1600PubMedCrossRef
Zurück zum Zitat Hughes I, Thalmann I, Thalmann R, Ornitz DM (2006) Mixing model systems: using zebrafish and mouse inner ear mutants and other organ systems to unravel the mystery of otoconial development. Brain Res 1091:58–74PubMedPubMedCentralCrossRef Hughes I, Thalmann I, Thalmann R, Ornitz DM (2006) Mixing model systems: using zebrafish and mouse inner ear mutants and other organ systems to unravel the mystery of otoconial development. Brain Res 1091:58–74PubMedPubMedCentralCrossRef
Zurück zum Zitat Ide M, Morimitsu T (1990) Long term effects of intense sound on endocochlear DC potential. Auris Nasus Larynx 17:1–10PubMedCrossRef Ide M, Morimitsu T (1990) Long term effects of intense sound on endocochlear DC potential. Auris Nasus Larynx 17:1–10PubMedCrossRef
Zurück zum Zitat Ikeda K, Kusakari J, Takasaka T (1988) Ionic changes in cochlear endolymph of the guinea pig induced by acoustic injury. Hear Res 32:103–110PubMedCrossRef Ikeda K, Kusakari J, Takasaka T (1988) Ionic changes in cochlear endolymph of the guinea pig induced by acoustic injury. Hear Res 32:103–110PubMedCrossRef
Zurück zum Zitat Johnson KR, Zheng QY, Erway LC (2000) A major gene affecting age-related hearing loss is common to at least 10 inbred strains of mice. Genomics 70:171–180PubMedCrossRef Johnson KR, Zheng QY, Erway LC (2000) A major gene affecting age-related hearing loss is common to at least 10 inbred strains of mice. Genomics 70:171–180PubMedCrossRef
Zurück zum Zitat Johnson KR, Longo-Guess CM, Gagnon LH (2012) Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia. PLoS One 7, e36074PubMedPubMedCentralCrossRef Johnson KR, Longo-Guess CM, Gagnon LH (2012) Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia. PLoS One 7, e36074PubMedPubMedCentralCrossRef
Zurück zum Zitat Kang C, Tian C, SoÌnnichsen FD, Smith JA, Meiler J, George AL Jr, Vanoye CG, Kim HJ, Sanders CR (2008) Structure of KCNE1 and implications for how it modulates the KCNQ1 potassium channel. Biochemistry 47:7999–8006PubMedPubMedCentralCrossRef Kang C, Tian C, SoÌnnichsen FD, Smith JA, Meiler J, George AL Jr, Vanoye CG, Kim HJ, Sanders CR (2008) Structure of KCNE1 and implications for how it modulates the KCNQ1 potassium channel. Biochemistry 47:7999–8006PubMedPubMedCentralCrossRef
Zurück zum Zitat Kazmierczak M, Harris SL, Kazmierczak P, Shah P, Starovoytov V, Ohlemiller KK, Schwander M (2015) Progressive hearing loss in mice carrying a mutation in Usp53. J Neurosci 35:15582–15598PubMedCrossRef Kazmierczak M, Harris SL, Kazmierczak P, Shah P, Starovoytov V, Ohlemiller KK, Schwander M (2015) Progressive hearing loss in mice carrying a mutation in Usp53. J Neurosci 35:15582–15598PubMedCrossRef
Zurück zum Zitat Kim H-J, Oh G-S, Lee J-H, Lyu A-R, Ji H-M, Lee S-H, Song J, Park S-J, You Y-O, Sul J-D, Park C, Chung S-Y, Moon S-K, Lim DJ, So H-S, Park R (2011) Cisplatin ototoxicity involves cytokines and STAT6 signaling network. Cell Res 21:944–956PubMedPubMedCentralCrossRef Kim H-J, Oh G-S, Lee J-H, Lyu A-R, Ji H-M, Lee S-H, Song J, Park S-J, You Y-O, Sul J-D, Park C, Chung S-Y, Moon S-K, Lim DJ, So H-S, Park R (2011) Cisplatin ototoxicity involves cytokines and STAT6 signaling network. Cell Res 21:944–956PubMedPubMedCentralCrossRef
Zurück zum Zitat Kim KX, Sanneman JD, Kim H-M, Harbidge DG, Xu J, Soleimani M, Wangemann P, Marcus DC (2014) Slc26a7 chloride channel activity and localization in mouse Reissner's membrane epithelium. PLoS One 9, e97191PubMedPubMedCentralCrossRef Kim KX, Sanneman JD, Kim H-M, Harbidge DG, Xu J, Soleimani M, Wangemann P, Marcus DC (2014) Slc26a7 chloride channel activity and localization in mouse Reissner's membrane epithelium. PLoS One 9, e97191PubMedPubMedCentralCrossRef
Zurück zum Zitat Kitajiri S-I, Fukumoto K, Hata M, Sasaki H, Katsuno T, Nakagawa T, Ito J, Tsukita S, Tsukita S (2004) Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia. J Cell Biol 166:559–570PubMedPubMedCentralCrossRef Kitajiri S-I, Fukumoto K, Hata M, Sasaki H, Katsuno T, Nakagawa T, Ito J, Tsukita S, Tsukita S (2004) Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia. J Cell Biol 166:559–570PubMedPubMedCentralCrossRef
Zurück zum Zitat Kitajiri S-I, Katsuno T, Sasaki H, Ito J, Furuse M, Tsukita S (2014) Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells. Biology Open, BIO20147799 Kitajiri S-I, Katsuno T, Sasaki H, Ito J, Furuse M, Tsukita S (2014) Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells. Biology Open, BIO20147799
Zurück zum Zitat Kobayashi T, Aslan A, Chiba T, Takasaka T, Sanna M (1996) Measurement of endocochlear DC potentials in ears with acoustic neuromas: a preliminary report. Acta Otolaryngol 116:791–795PubMedCrossRef Kobayashi T, Aslan A, Chiba T, Takasaka T, Sanna M (1996) Measurement of endocochlear DC potentials in ears with acoustic neuromas: a preliminary report. Acta Otolaryngol 116:791–795PubMedCrossRef
Zurück zum Zitat Kohonen A, Jauhiainen T, Liewendahl K, Tarkkanen J, Kaimio M (1971) Deafness in experimental hypo- and hyperthyroidism. Laryngoscope 81:947–956PubMedCrossRef Kohonen A, Jauhiainen T, Liewendahl K, Tarkkanen J, Kaimio M (1971) Deafness in experimental hypo- and hyperthyroidism. Laryngoscope 81:947–956PubMedCrossRef
Zurück zum Zitat Konishi T, Salt AN, Hamrick PE (1979) Effects of exposure to noise on ion movement in guinea pig cochlea. Hear Res 1:325–342PubMedCrossRef Konishi T, Salt AN, Hamrick PE (1979) Effects of exposure to noise on ion movement in guinea pig cochlea. Hear Res 1:325–342PubMedCrossRef
Zurück zum Zitat Lee JH, Chiba T, Marcus DC (2001) P2X2 receptor mediates stimulation of parasensory cation absorption by cochlear outer sulcus cells and vestibular transitional cells. J Neurosci 21:9168–9174PubMed Lee JH, Chiba T, Marcus DC (2001) P2X2 receptor mediates stimulation of parasensory cation absorption by cochlear outer sulcus cells and vestibular transitional cells. J Neurosci 21:9168–9174PubMed
Zurück zum Zitat Leonova EV, Fairfield DA, Lomax MI, Altschuler RA (2002) Constitutive expression of Hsp27 in the rat cochlea. Hear Res 163:61–70PubMedCrossRef Leonova EV, Fairfield DA, Lomax MI, Altschuler RA (2002) Constitutive expression of Hsp27 in the rat cochlea. Hear Res 163:61–70PubMedCrossRef
Zurück zum Zitat Melichar I, Syka J, Ulehlova L (1980) Recovery of the endocochlear potential and the K+ concentrations in the cochlear fluids after acoustic trauma. Hear Res 2:55–63PubMedCrossRef Melichar I, Syka J, Ulehlova L (1980) Recovery of the endocochlear potential and the K+ concentrations in the cochlear fluids after acoustic trauma. Hear Res 2:55–63PubMedCrossRef
Zurück zum Zitat Meltser I, Tahera Y, Simpson EM, Hultcrantz M, Charitidi K, Gustafsson J-A, Canlon B (2008) Estrogen receptor B protects against acoustic trauma in mice. J Clin Investig 118:1563–1570PubMedPubMedCentralCrossRef Meltser I, Tahera Y, Simpson EM, Hultcrantz M, Charitidi K, Gustafsson J-A, Canlon B (2008) Estrogen receptor B protects against acoustic trauma in mice. J Clin Investig 118:1563–1570PubMedPubMedCentralCrossRef
Zurück zum Zitat Meyer zum Gottesberge AM, Massing T, Hansen S (2012) Missing mitochondrial Mpv17 gene function induces tissue-specific dell-death pathway in the degenerating inner ear. Cell Tissue Res 347:343–356PubMedCrossRef Meyer zum Gottesberge AM, Massing T, Hansen S (2012) Missing mitochondrial Mpv17 gene function induces tissue-specific dell-death pathway in the degenerating inner ear. Cell Tissue Res 347:343–356PubMedCrossRef
Zurück zum Zitat Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC (2002) Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6. Hum Mol Genet 11:1887–1898PubMedCrossRef Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC (2002) Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6. Hum Mol Genet 11:1887–1898PubMedCrossRef
Zurück zum Zitat Mockett BG, Housley GD, Thorne PR (1994) Fluorescence imaging of extracellular purinergic sites and putative ecto-ATPase sites on isolated cochlear hair cells. J Neurosci 14:1692–1707 Mockett BG, Housley GD, Thorne PR (1994) Fluorescence imaging of extracellular purinergic sites and putative ecto-ATPase sites on isolated cochlear hair cells. J Neurosci 14:1692–1707
Zurück zum Zitat Morozko EL, Nishio A, Ingham NJ, Chandra R, Fitzgerald T, Martelletti E, Borck G, Wilson E, Riordan GP, Wangemann P, Forge A, Steel KP, Liddle RA, Friedman TB, Belyantseva IA (2014) ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells. Hum Mol Genet 24(3):609–624PubMedPubMedCentralCrossRef Morozko EL, Nishio A, Ingham NJ, Chandra R, Fitzgerald T, Martelletti E, Borck G, Wilson E, Riordan GP, Wangemann P, Forge A, Steel KP, Liddle RA, Friedman TB, Belyantseva IA (2014) ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells. Hum Mol Genet 24(3):609–624PubMedPubMedCentralCrossRef
Zurück zum Zitat Nagashima R, Yamaguchi T, Tanaka H, Ogita K (2010) Mechanism underlying the protective effect of tempol and Nw-Nitro-L-Arginine Methyl Ester on acoustic injury: possible involvement of c-Jun N-Terminal Kinase pathway and Connexin26 in the cochlear spiral ligament. J Pharmacol 114:50–62 Nagashima R, Yamaguchi T, Tanaka H, Ogita K (2010) Mechanism underlying the protective effect of tempol and Nw-Nitro-L-Arginine Methyl Ester on acoustic injury: possible involvement of c-Jun N-Terminal Kinase pathway and Connexin26 in the cochlear spiral ligament. J Pharmacol 114:50–62
Zurück zum Zitat Nagtegaal AP, Spijker S, Crins TTH, Borst JGG (2012) A novel QTL underlying early-onset, low-frequency hearing loss in BXD recombinant inbred strains. Genes Brain Behav 11:911–920PubMed Nagtegaal AP, Spijker S, Crins TTH, Borst JGG (2012) A novel QTL underlying early-onset, low-frequency hearing loss in BXD recombinant inbred strains. Genes Brain Behav 11:911–920PubMed
Zurück zum Zitat Nakano Y, Kim SH, Kim H-M, Sanneman JD, Zhang Y, Smith RJH, Marcus DC, Wangemann P, Nessler RA, Banfi B (2009) A claudin-9-based ion permeability barrier is essential for hearing. PLoS Genet 5, e1000610PubMedPubMedCentralCrossRef Nakano Y, Kim SH, Kim H-M, Sanneman JD, Zhang Y, Smith RJH, Marcus DC, Wangemann P, Nessler RA, Banfi B (2009) A claudin-9-based ion permeability barrier is essential for hearing. PLoS Genet 5, e1000610PubMedPubMedCentralCrossRef
Zurück zum Zitat Nayak G, Lee SI, Yousaf R, Edelmann SE, Trincot C, Van Itallie CM, Sinha GP, Rafeeq M, Jones SM, Belyantseva IA, Anderson JM, Forge A, Frolenkov G, Riazuuddin S (2013) Tricellulin deficiency affects tight junction architecture and cochlear hair cells. J Clin Investig 123:4036–4049PubMedPubMedCentralCrossRef Nayak G, Lee SI, Yousaf R, Edelmann SE, Trincot C, Van Itallie CM, Sinha GP, Rafeeq M, Jones SM, Belyantseva IA, Anderson JM, Forge A, Frolenkov G, Riazuuddin S (2013) Tricellulin deficiency affects tight junction architecture and cochlear hair cells. J Clin Investig 123:4036–4049PubMedPubMedCentralCrossRef
Zurück zum Zitat Nemoto M, Morita Y, Mishima Y, Takahashi S, Nomura T, Ushiki T, Shiroishi T, Kikkawa Y, Yonekawa H, Kominami R (2004) Ahl3, a third locus on mouse chromosome 17 affecting age-related hearing loss. Biochem Biophys Res Commun 324:1283–1288PubMedCrossRef Nemoto M, Morita Y, Mishima Y, Takahashi S, Nomura T, Ushiki T, Shiroishi T, Kikkawa Y, Yonekawa H, Kominami R (2004) Ahl3, a third locus on mouse chromosome 17 affecting age-related hearing loss. Biochem Biophys Res Commun 324:1283–1288PubMedCrossRef
Zurück zum Zitat Nie L, Xu T, Mo J, Zhang Y, Feng W, Vazquez AE, Morris K, Beisel K, Yamoah EN (2006) Molecular cloning and functional study of KCNQ4 channels in the mouse inner ear. FASEB J 20:A1368 Nie L, Xu T, Mo J, Zhang Y, Feng W, Vazquez AE, Morris K, Beisel K, Yamoah EN (2006) Molecular cloning and functional study of KCNQ4 channels in the mouse inner ear. FASEB J 20:A1368
Zurück zum Zitat Nin F, Hibino H, Doi KS, Suzuki T, Hisa Y, Kurachi Y (2008) The endocochlear potential depends on two K+ diffusion potentials and an electrical barrier in the stria vascularis of the inner ear. Proc Natl Acad Sci U S A 105:1751–1756PubMedPubMedCentralCrossRef Nin F, Hibino H, Doi KS, Suzuki T, Hisa Y, Kurachi Y (2008) The endocochlear potential depends on two K+ diffusion potentials and an electrical barrier in the stria vascularis of the inner ear. Proc Natl Acad Sci U S A 105:1751–1756PubMedPubMedCentralCrossRef
Zurück zum Zitat Noben-Trauth K, Zheng QY, Johnson KR (2003) Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet 35:21–23PubMedPubMedCentralCrossRef Noben-Trauth K, Zheng QY, Johnson KR (2003) Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet 35:21–23PubMedPubMedCentralCrossRef
Zurück zum Zitat Noben-Trauth K, Latoche JR, Neely HR, Bennett B (2010) Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice. PLoS One 5, e11459PubMedPubMedCentralCrossRef Noben-Trauth K, Latoche JR, Neely HR, Bennett B (2010) Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice. PLoS One 5, e11459PubMedPubMedCentralCrossRef
Zurück zum Zitat Nordmann AS, Bohne BA, Harding GW (2000) Histopathological differences between temporary and permanent threshold shift. Hear Res 139:13–30PubMedCrossRef Nordmann AS, Bohne BA, Harding GW (2000) Histopathological differences between temporary and permanent threshold shift. Hear Res 139:13–30PubMedCrossRef
Zurück zum Zitat Oh SH, Adler HJ, Raphael Y, Lomax MI (2002) WDR1 colocalizes with ADF and actin in the normal and noise-damaged chick cochlea. J Comp Neurol 448:399–409PubMedCrossRef Oh SH, Adler HJ, Raphael Y, Lomax MI (2002) WDR1 colocalizes with ADF and actin in the normal and noise-damaged chick cochlea. J Comp Neurol 448:399–409PubMedCrossRef
Zurück zum Zitat Ohlemiller KK (2002) Reduction in sharpness of frequency tuning but not endocochlear potential in aging and noise-exposed BALB/cJ mice. J Assoc Res Otolaryngol 3:444–456PubMedPubMedCentralCrossRef Ohlemiller KK (2002) Reduction in sharpness of frequency tuning but not endocochlear potential in aging and noise-exposed BALB/cJ mice. J Assoc Res Otolaryngol 3:444–456PubMedPubMedCentralCrossRef
Zurück zum Zitat Ohlemiller KK, Lett JM, Gagnon PM (2006) Cellular correlates of age-related endocochlear potential reduction in a mouse model. Hear Res 220:10–26PubMedCrossRef Ohlemiller KK, Lett JM, Gagnon PM (2006) Cellular correlates of age-related endocochlear potential reduction in a mouse model. Hear Res 220:10–26PubMedCrossRef
Zurück zum Zitat Ohlemiller KK, Rice MR, Lett JM, Gagnon PM (2009) Absence of strial melanin coincides with age associated marginal cell loss and endocochlear potential decline. Hear Res 249:1–14PubMedCrossRef Ohlemiller KK, Rice MR, Lett JM, Gagnon PM (2009) Absence of strial melanin coincides with age associated marginal cell loss and endocochlear potential decline. Hear Res 249:1–14PubMedCrossRef
Zurück zum Zitat Ohlemiller KK, Rosen AD, Gagnon PM (2010a) A major effect QTL on chromosome 18 for noise injury to the mouse cochlear lateral wall. Hear Res 260:47–53PubMedPubMedCentralCrossRef Ohlemiller KK, Rosen AD, Gagnon PM (2010a) A major effect QTL on chromosome 18 for noise injury to the mouse cochlear lateral wall. Hear Res 260:47–53PubMedPubMedCentralCrossRef
Zurück zum Zitat Ohlemiller KK, Dahl AR, Gagnon PM (2010b) Divergent aging characteristics in CBA/J and CBA/CaJ mouse cochleae. J Assoc Res Otolaryngol 11:605–623PubMedPubMedCentralCrossRef Ohlemiller KK, Dahl AR, Gagnon PM (2010b) Divergent aging characteristics in CBA/J and CBA/CaJ mouse cochleae. J Assoc Res Otolaryngol 11:605–623PubMedPubMedCentralCrossRef
Zurück zum Zitat Ohlemiller KK, Rosen AR, Rellinger EA, Montgomery SC, Gagnon PM (2011) Different cellular and genetic basis of noise-related endocochlear potential reduction in CBA/J and BALB/cJ mice. J Assoc Res Otolaryngol 12:45–58PubMedPubMedCentralCrossRef Ohlemiller KK, Rosen AR, Rellinger EA, Montgomery SC, Gagnon PM (2011) Different cellular and genetic basis of noise-related endocochlear potential reduction in CBA/J and BALB/cJ mice. J Assoc Res Otolaryngol 12:45–58PubMedPubMedCentralCrossRef
Zurück zum Zitat Okamoto Y, Hoya N, Kamiya K, Fujii M, Ogawa K, Matsunaga T (2005) Permanent threshold shift caused by acute cochlear mitochondrial dysfunction is primarily mediated by degeneration of the lateral wall of the cochlea. Audiol Neuro Otol 10:220–233CrossRef Okamoto Y, Hoya N, Kamiya K, Fujii M, Ogawa K, Matsunaga T (2005) Permanent threshold shift caused by acute cochlear mitochondrial dysfunction is primarily mediated by degeneration of the lateral wall of the cochlea. Audiol Neuro Otol 10:220–233CrossRef
Zurück zum Zitat Oyamada M, Takebe K, Oyamada Y (2013) Regulation of connexin expression by transcription factors and epigenetic mechanisms. Biochim Biophys Acta Biomembr 1828:118–133CrossRef Oyamada M, Takebe K, Oyamada Y (2013) Regulation of connexin expression by transcription factors and epigenetic mechanisms. Biochim Biophys Acta Biomembr 1828:118–133CrossRef
Zurück zum Zitat Riccomagno MM, Martinu L, Mulheisen M, Wu DK, Epstein DJ (2002) Specification of the mammalian cochlea is dependent on Sonic hedgehog. Genes Dev 16:2365–2378PubMedPubMedCentralCrossRef Riccomagno MM, Martinu L, Mulheisen M, Wu DK, Epstein DJ (2002) Specification of the mammalian cochlea is dependent on Sonic hedgehog. Genes Dev 16:2365–2378PubMedPubMedCentralCrossRef
Zurück zum Zitat Royaux IE, Suzuki K, Mori A, Katoh R, Everett LA, Kohn LD, Green ED (2000) Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. Endocrinology 141:839–845PubMedCrossRef Royaux IE, Suzuki K, Mori A, Katoh R, Everett LA, Kohn LD, Green ED (2000) Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. Endocrinology 141:839–845PubMedCrossRef
Zurück zum Zitat Rudnicki A, Isakov O, Ushakov K, Shivatzki S, Weiss I, Friedman LM, Shomron N, Avraham KB (2014) Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways. BMC Genomics 15:484PubMedPubMedCentralCrossRef Rudnicki A, Isakov O, Ushakov K, Shivatzki S, Weiss I, Friedman LM, Shomron N, Avraham KB (2014) Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways. BMC Genomics 15:484PubMedPubMedCentralCrossRef
Zurück zum Zitat Salt AN, Konishi T (1979) Effects of noise on cochlear potentials and endolymph potassium concentrations recorded with ion-selective electrodes. Hear Res 1:343–363PubMedCrossRef Salt AN, Konishi T (1979) Effects of noise on cochlear potentials and endolymph potassium concentrations recorded with ion-selective electrodes. Hear Res 1:343–363PubMedCrossRef
Zurück zum Zitat Schmiedt RA (1993) Cochlear potentials in quiet-aged gerbils: does the aging cochlea need a jump start? In: Verillo RT (ed) Sensory research: multimodal perspectives. Lawrence Erlbaum, Hillsdale, pp 91–103 Schmiedt RA (1993) Cochlear potentials in quiet-aged gerbils: does the aging cochlea need a jump start? In: Verillo RT (ed) Sensory research: multimodal perspectives. Lawrence Erlbaum, Hillsdale, pp 91–103
Zurück zum Zitat Schuknecht HF, Gacek MR (1993) Cochlear pathology in presbycusis. Ann Otol Rhinol Laryngol 102:1–16PubMedCrossRef Schuknecht HF, Gacek MR (1993) Cochlear pathology in presbycusis. Ann Otol Rhinol Laryngol 102:1–16PubMedCrossRef
Zurück zum Zitat Schuknecht HF, Watanuki K, Takahashi T, Belal AA, Kimura RS, Jones DD (1974) Atrophy of the stria vascularis, a common cause for hearing loss. Laryngoscope 84:1777–1821PubMedCrossRef Schuknecht HF, Watanuki K, Takahashi T, Belal AA, Kimura RS, Jones DD (1974) Atrophy of the stria vascularis, a common cause for hearing loss. Laryngoscope 84:1777–1821PubMedCrossRef
Zurück zum Zitat Selvakumar D, Drescher MJ, Dowdall JR, Khan KM, Hatfield JS, Ramakrishnan NA, Drescher DG (2012) CNGA3 is expressed in inner ear hair cells and binds to an intracellular C-terminus domain of EMILIN1. Biochem J 443:463–476PubMedCrossRef Selvakumar D, Drescher MJ, Dowdall JR, Khan KM, Hatfield JS, Ramakrishnan NA, Drescher DG (2012) CNGA3 is expressed in inner ear hair cells and binds to an intracellular C-terminus domain of EMILIN1. Biochem J 443:463–476PubMedCrossRef
Zurück zum Zitat Sewell W (1984) The effects of furosemide on the endocochlear potential and auditory nerve fiber tuning curves in cats. Hear Res 14:305–314PubMedCrossRef Sewell W (1984) The effects of furosemide on the endocochlear potential and auditory nerve fiber tuning curves in cats. Hear Res 14:305–314PubMedCrossRef
Zurück zum Zitat Spicer SS, Schulte BA (2005) Pathologic changes of presbycusis begin in secondary processes and spread to primary processes of strial marginal cells. Hear Res 205:225–240PubMedCrossRef Spicer SS, Schulte BA (2005) Pathologic changes of presbycusis begin in secondary processes and spread to primary processes of strial marginal cells. Hear Res 205:225–240PubMedCrossRef
Zurück zum Zitat Spiess AC, Lang H, Schulte BA, Spicer SS, Schmiedt RA (2002) Effects of gap junction uncoupling in the gerbil cochlea. Laryngoscope 112:1635–1641PubMedCrossRef Spiess AC, Lang H, Schulte BA, Spicer SS, Schmiedt RA (2002) Effects of gap junction uncoupling in the gerbil cochlea. Laryngoscope 112:1635–1641PubMedCrossRef
Zurück zum Zitat Summers KM, Bokil NJ, Lu FT, Low JT, Baisden JM, Duffy D, Radford DJ (2010) Mutations at KCNQ1 and an unknown locus cause long QT syndrome in a large Australian family: implications for genetic testing. Am J Med Genet A 152:613–621CrossRef Summers KM, Bokil NJ, Lu FT, Low JT, Baisden JM, Duffy D, Radford DJ (2010) Mutations at KCNQ1 and an unknown locus cause long QT syndrome in a large Australian family: implications for genetic testing. Am J Med Genet A 152:613–621CrossRef
Zurück zum Zitat Takumida M, Takumida S, Anniko M (2014) Localization of sirtuins in the mouse inner ear. Acta Otolaryngol 134:331–338PubMedCrossRef Takumida M, Takumida S, Anniko M (2014) Localization of sirtuins in the mouse inner ear. Acta Otolaryngol 134:331–338PubMedCrossRef
Zurück zum Zitat Tran Ba Huy P, Ferrary E, Roinel N (1989) Electrochemical and clinical observations in 11 cases of Meniere's disease. In: Nadol JB (ed) Meniere's disease. Kugler and Ghedini, Amsterdam, pp 241–246 Tran Ba Huy P, Ferrary E, Roinel N (1989) Electrochemical and clinical observations in 11 cases of Meniere's disease. In: Nadol JB (ed) Meniere's disease. Kugler and Ghedini, Amsterdam, pp 241–246
Zurück zum Zitat Varma S, Cao Y, Tagne J-B, Lakshminarayanan M, Li J, Friedman TB, Morell RJ, Warburton D, Kotton DN, Ramirez MI (2012) The transcription factors Grainyhead-like 2 and NK2-homeobox 1 form a regulatory loop that coordinates lung epithelial cell morphogenesis and differentiation. J Biol Chem 287:37282–37295PubMedPubMedCentralCrossRef Varma S, Cao Y, Tagne J-B, Lakshminarayanan M, Li J, Friedman TB, Morell RJ, Warburton D, Kotton DN, Ramirez MI (2012) The transcription factors Grainyhead-like 2 and NK2-homeobox 1 form a regulatory loop that coordinates lung epithelial cell morphogenesis and differentiation. J Biol Chem 287:37282–37295PubMedPubMedCentralCrossRef
Zurück zum Zitat Vassout P (1984) Effects of pure tone on endocochlear potential and potassium ion concentration in the guinea pig cochlea. Acta OtoLaryngol 98:199–203PubMedCrossRef Vassout P (1984) Effects of pure tone on endocochlear potential and potassium ion concentration in the guinea pig cochlea. Acta OtoLaryngol 98:199–203PubMedCrossRef
Zurück zum Zitat Wang W, Lufkin T (2005) Hmx homeobox gene function in inner ear and nervous system cell-type specification and development. Exp Cell Res 306:373–379PubMedCrossRef Wang W, Lufkin T (2005) Hmx homeobox gene function in inner ear and nervous system cell-type specification and development. Exp Cell Res 306:373–379PubMedCrossRef
Zurück zum Zitat Wang J, Li Q, Dong W, Chen J (1992) Effects of various noise exposures on endocochlear potentials correlated with cochlear gross responses. Hear Res 59:31–38PubMedCrossRef Wang J, Li Q, Dong W, Chen J (1992) Effects of various noise exposures on endocochlear potentials correlated with cochlear gross responses. Hear Res 59:31–38PubMedCrossRef
Zurück zum Zitat Wang Y, Hirose K, Liberman MC (2002) Dynamics of noise-induced cellular injury and repair in the mouse cochlea. J Assoc Res Otolaryngol 3:248–268PubMedPubMedCentralCrossRef Wang Y, Hirose K, Liberman MC (2002) Dynamics of noise-induced cellular injury and repair in the mouse cochlea. J Assoc Res Otolaryngol 3:248–268PubMedPubMedCentralCrossRef
Zurück zum Zitat Watanabe K, Takeda K, Katori Y, Ikeda K, Oshima T, Yasumoto K, Saito H, Takasaka T, Shibahara S (2000) Expression of the Sox10 gene during mouse inner ear development. Mol Brain Res 84:141–145PubMedCrossRef Watanabe K, Takeda K, Katori Y, Ikeda K, Oshima T, Yasumoto K, Saito H, Takasaka T, Shibahara S (2000) Expression of the Sox10 gene during mouse inner ear development. Mol Brain Res 84:141–145PubMedCrossRef
Zurück zum Zitat Willott JF, Turner JG, Carlson S, Ding D, Bross LS, Falls WA (1998) The BALB/c mouse as an animal model for progressive sensorineural hearing loss. Hear Res 115:162–174PubMedCrossRef Willott JF, Turner JG, Carlson S, Ding D, Bross LS, Falls WA (1998) The BALB/c mouse as an animal model for progressive sensorineural hearing loss. Hear Res 115:162–174PubMedCrossRef
Zurück zum Zitat Xiao S-M, Kung AWC, Gao Y, Lau KS, Ma A, Zhang ZL, Liu JM, Xia W, He J-W, Zhao L, Nie M, Fu WZ, Zhang MJ, Sun J, Kwan JSH, Tso GHW, Dai ZJ, Cheung CL, Bow CH, Leung AYH, Tan KCB, Sham PC (2012) Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density. Hum Mol Genet 21:1648–1657PubMedCrossRef Xiao S-M, Kung AWC, Gao Y, Lau KS, Ma A, Zhang ZL, Liu JM, Xia W, He J-W, Zhao L, Nie M, Fu WZ, Zhang MJ, Sun J, Kwan JSH, Tso GHW, Dai ZJ, Cheung CL, Bow CH, Leung AYH, Tan KCB, Sham PC (2012) Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density. Hum Mol Genet 21:1648–1657PubMedCrossRef
Zurück zum Zitat Yang H, Zhao X, Xu Y, Wang L, He A, Lundberg YW (2011) Matrix recruitment and calcium sequestration for spatial specific otoconia development. PLoS One 6, e20498PubMedPubMedCentralCrossRef Yang H, Zhao X, Xu Y, Wang L, He A, Lundberg YW (2011) Matrix recruitment and calcium sequestration for spatial specific otoconia development. PLoS One 6, e20498PubMedPubMedCentralCrossRef
Metadaten
Titel
QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice
verfasst von
Kevin K. Ohlemiller
Anna L. Kiener
Patricia M. Gagnon
Publikationsdatum
15.03.2016
Verlag
Springer US
Erschienen in
Journal of the Association for Research in Otolaryngology / Ausgabe 3/2016
Print ISSN: 1525-3961
Elektronische ISSN: 1438-7573
DOI
https://doi.org/10.1007/s10162-016-0558-8

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