RESUMO
Mutations in voltage-gated potassium channel KCNE1 cause Jervell and Lange-Nielsen syndrome type 2 (JLNS2), resulting in congenital deafness and vestibular dysfunction. We conducted gene therapy by injecting viral vectors using the canalostomy approach in Kcne1-/- mice to treat both the hearing and vestibular symptoms. Results showed early treatment prevented collapse of the Reissner's membrane and vestibular wall, retained the normal size of the semicircular canals, and prevented the degeneration of inner ear cells. In a dose-dependent manner, the treatment preserved auditory (16 out of 20 mice) and vestibular (20/20) functions in mice treated with the high-dosage for at least five months. In the low-dosage group, a subgroup of mice (13/20) showed improvements only in the vestibular functions. Results supported that highly efficient transduction is one of the key factors for achieving the efficacy and maintaining the long-term therapeutic effect. Secondary outcomes of treatment included improved birth and litter survival rates. Our results demonstrated that gene therapy via the canalostomy approach, which has been considered to be one of the more feasible delivery methods for human inner ear gene therapy, preserved auditory and vestibular functions in a dose-dependent manner in a mouse model of JLNS2.
Assuntos
Terapia Genética/métodos , Vetores Genéticos/administração & dosagem , Síndrome de Jervell-Lange Nielsen/terapia , Canais de Potássio de Abertura Dependente da Tensão da Membrana/genética , Canais Semicirculares/cirurgia , Animais , Animais Recém-Nascidos , Dependovirus , Modelos Animais de Doenças , Feminino , Vetores Genéticos/genética , Audição/genética , Humanos , Injeções/métodos , Síndrome de Jervell-Lange Nielsen/genética , Masculino , Camundongos , Camundongos Knockout , Parvovirinae/genética , Propriocepção/genéticaRESUMO
Wolfram syndrome (WS) is caused by recessive mutations in the Wolfram syndrome 1 (WFS1) gene. Sensorineural hearing impairment (HI) is a frequent feature in WS and, furthermore, certain mutations in WFS1 cause nonsyndromic dominantly inherited low-frequency sensorineural HI. These two phenotypes are clinically distinct indicating that WFS1 is a reasonable candidate for genetic studies in patients with other phenotypes of HI. Here we have investigated, whether the variation in WFS1 has a pathogenic role in age-related hearing impairment (ARHI). WFS1 gene was investigated in a population sample of 518 Finnish adults born in 1938-1949 and representing variable hearing phenotypes. Identified variants were evaluated with respect to pathogenic potential. A rare mutation predicted to be pathogenic was found in a family with many members with impaired hearing. Twenty members were recruited to a segregation study and a detailed clinical examination. Heterozygous p.Tyr528His variant segregated completely with late-onset HI in which hearing deteriorated first at high frequencies and progressed to mid and low frequencies later in life. We report the first mutation in the WFS1 gene causing late-onset HI with audiogram configurations typical for ARHI. Monogenic forms of ARHI are rare and our results add WFS1 to the short list of such genes.
Assuntos
Perda Auditiva Neurossensorial/genética , Audição/genética , Proteínas de Membrana/genética , Mutação , Presbiacusia/genética , Estimulação Acústica , Adolescente , Adulto , Fatores Etários , Idade de Início , Idoso , Idoso de 80 Anos ou mais , Envelhecimento/genética , Audiometria de Tons Puros , Análise Mutacional de DNA , Feminino , Finlândia , Predisposição Genética para Doença , Perda Auditiva Neurossensorial/diagnóstico , Perda Auditiva Neurossensorial/fisiopatologia , Heterozigoto , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Fenótipo , Presbiacusia/diagnóstico , Presbiacusia/fisiopatologia , Adulto JovemRESUMO
BACKGROUND: Noise-induced hearing loss (NIHL) is a multifactorial disease, and dysregulation of oxidative stress is universally acknowledged as one crucial pathogenic factor for this disease. Recently studies have found the LncRNA HOTAIR is involved in the alteration of oxidative stress level, cell proliferation, cell cycle progression, and apoptosis. Considering the effects of lncRNA HOTAIR in cellular oxidative stress, we sought to investigate the influence of lncRNA HOTAIR variants on the risk of NIHL. METHODS: To explore the effects of HOTAIR polymorphisms on individual susceptibility to NIHL, We performed genotyping of three tagSNPs (rs874945, rs4759314 and rs7958904) in HOTAIR gene in a Chinese population which consists of 570 NIHL cases and 570 controls. The luciferase assays were further performed to investigate the regulatory function of HOTAIR tagSNPs. RESULTS: Our results revealed individuals with the G allele of HOTAIR tagSNP rs4759314 and the haplotype (rs874945, rs4759314 and rs7958904) are associated with an increased risk of NIHL in a Chinese population. Meanwhile, the rs4759314 G allele could significantly increase the expression of lncRNA HOTAIR. CONCLUSIONS: The genetic polymorphism within HOTAIR gene may play a crucial role in the occurrence and development of NIHL.
Assuntos
Perda Auditiva Provocada por Ruído/genética , Audição/genética , Polimorfismo de Nucleotídeo Único , RNA Longo não Codificante/genética , Estimulação Acústica , Adulto , Animais , Povo Asiático/genética , Limiar Auditivo , Estudos de Casos e Controles , Linhagem Celular , China , Feminino , Regulação da Expressão Gênica , Frequência do Gene , Estudos de Associação Genética , Predisposição Genética para Doença , Haplótipos , Perda Auditiva Provocada por Ruído/diagnóstico , Perda Auditiva Provocada por Ruído/etnologia , Perda Auditiva Provocada por Ruído/fisiopatologia , Testes Auditivos , Humanos , Masculino , Camundongos , Pessoa de Meia-Idade , Fenótipo , Regiões Promotoras Genéticas , TransfecçãoRESUMO
Auditory efferent neurons reside in the brain and innervate the sensory hair cells of the cochlea to modulate incoming acoustic signals. Two groups of efferents have been described in mouse and this report will focus on the medial olivocochlear (MOC) system. Electrophysiological data suggest the MOC efferents function in selective listening by differentially attenuating auditory nerve fiber activity in quiet and noisy conditions. Because speech understanding in noise is impaired in age-related hearing loss, we asked whether pathologic changes in input to MOC neurons from higher centers could be involved. The present study investigated the anatomical nature of descending projections from the inferior colliculus (IC) to MOCs in 3-month old mice with normal hearing, and in 6-month old mice with normal hearing (CBA/CaH), early onset progressive hearing loss (DBA/2), and congenital deafness (homozygous Shaker-2). Anterograde tracers were injected into the IC and retrograde tracers into the cochlea. Electron microscopic analysis of double-labelled tissue confirmed direct synaptic contact from the IC onto MOCs in all cohorts. These labelled terminals are indicative of excitatory neurotransmission because they contain round synaptic vesicles, exhibit asymmetric membrane specializations, and are co-labelled with antibodies against VGlut2, a glutamate transporter. 3D reconstructions of the terminal fields indicate that in normal hearing mice, descending projections from the IC are arranged tonotopically with low frequencies projecting laterally and progressively higher frequencies projecting more medially. Along the mediolateral axis, the projections of DBA/2 mice with acquired high frequency hearing loss were shifted medially towards expected higher frequency projecting regions. Shaker-2 mice with congenital deafness had a much broader spatial projection, revealing abnormalities in the topography of connections. These data suggest that loss in precision of IC directed MOC activation could contribute to impaired signal detection in noise.
Assuntos
Cóclea/inervação , Surdez/fisiopatologia , Audição , Colículos Inferiores/fisiopatologia , Núcleo Olivar/fisiopatologia , Estimulação Acústica , Animais , Vias Auditivas/fisiopatologia , Percepção Auditiva , Comportamento Animal , Surdez/metabolismo , Surdez/patologia , Surdez/psicologia , Modelos Animais de Doenças , Potenciais Evocados Auditivos do Tronco Encefálico , Predisposição Genética para Doença , Audição/genética , Colículos Inferiores/metabolismo , Colículos Inferiores/ultraestrutura , Camundongos Endogâmicos CBA , Camundongos Endogâmicos DBA , Camundongos Knockout , Microscopia Eletrônica de Transmissão , Miosinas/deficiência , Miosinas/genética , Técnicas de Rastreamento Neuroanatômico , Núcleo Olivar/metabolismo , Núcleo Olivar/ultraestrutura , Fenótipo , Detecção de Sinal Psicológico , Sinapses/ultraestrutura , Proteína Vesicular 2 de Transporte de Glutamato/metabolismoRESUMO
Studies of congenital and early-onset deafness have demonstrated that an absence of peripheral sound-evoked activity in the auditory nerve causes pathological changes in central auditory structures. The aim of this study was to establish whether progressive acquired hearing loss could lead to similar brain changes that would degrade the precision of signal transmission. We used complementary physiologic hearing tests and microscopic techniques to study the combined effect of both magnitude and duration of hearing loss on one of the first auditory synapses in the brain, the endbulb of Held (EB), along with its bushy cell (BC) target in the anteroventral cochlear nucleus. We compared two hearing mouse strains (CBA/Ca and heterozygous shaker-2+/-) against a model of early-onset progressive hearing loss (DBA/2) and a model of congenital deafness (homozygous shaker-2-/-), examining each strain at 1, 3, and 6 months of age. Furthermore, we employed a frequency model of the mouse cochlear nucleus to constrain our analyses to regions most likely to exhibit graded changes in hearing function with time. No significant differences in the gross morphology of EB or BC structure were observed in 1-month-old animals, indicating uninterrupted development. However, in animals with hearing loss, both EBs and BCs exhibited a graded reduction in size that paralleled the hearing loss, with the most severe pathology seen in deaf 6-month-old shaker-2-/- mice. Ultrastructural pathologies associated with hearing loss were less dramatic: minor changes were observed in terminal size but mitochondrial fraction and postsynaptic densities remained relatively stable. These results indicate that acquired progressive hearing loss can have consequences on auditory brain structure, with prolonged loss leading to greater pathologies. Our findings suggest a role for early intervention with assistive devices in order to mitigate long-term pathology and loss of function.
Assuntos
Nervo Coclear/ultraestrutura , Núcleo Coclear/ultraestrutura , Perda Auditiva/patologia , Audição , Sinapses/ultraestrutura , Estimulação Acústica , Fatores Etários , Animais , Limiar Auditivo , Comportamento Animal , Nervo Coclear/fisiopatologia , Núcleo Coclear/fisiopatologia , Modelos Animais de Doenças , Progressão da Doença , Potenciais Evocados Auditivos do Tronco Encefálico , Feminino , Predisposição Genética para Doença , Audição/genética , Perda Auditiva/genética , Perda Auditiva/fisiopatologia , Perda Auditiva/psicologia , Masculino , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos CBA , Camundongos Endogâmicos DBA , Camundongos Knockout , Microscopia Eletrônica de Transmissão , Miosinas/deficiência , Miosinas/genética , Fenótipo , Índice de Gravidade de Doença , Fatores de TempoRESUMO
Age-related hearing loss (AHL) is a progressive neurodegenerative disease that is largely silent in its initial stages. There is no sensitive blood biomarker for diagnosis or early detection of AHL. MicroRNAs (miRNAs or miRs) are abundant and highly stable in blood, and have been recently described as powerful circulating biomarkers in a wide range of diseases. In the present study, we identified concordant increases in miR-34a levels in the cochlea, auditory cortex, and plasma of C57BL/6 mice during aging. These increases were accompanied by elevated hearing thresholds and greater loss of hair cells. Levels of miR-34a targets, silent information regulator 1 (SIRT1), B-cell lymphoma-2 (Bcl-2), and E2F transcription factor 3 (E2F3), in the cochlea, auditory cortex, and plasma decreased with aging inversely to miR-34a. Moreover, plasma miR-34a levels were significantly higher in patients with AHL compared with controls who had normal hearing and had a receiver-operating characteristic curve that distinguished AHL patients from controls. However, SIRT1, Bcl-2, and E2F3 showed no correlation with AHL in humans. In summary, circulating miR-34a level may potentially serve as a useful biomarker for early detection of AHL.
Assuntos
Audição/genética , MicroRNAs/sangue , Presbiacusia/genética , Estimulação Acústica , Adulto , Fatores Etários , Animais , Área Sob a Curva , Audiometria de Tons Puros , Córtex Auditivo/metabolismo , Córtex Auditivo/fisiopatologia , Limiar Auditivo , Estudos de Casos e Controles , Cóclea/metabolismo , Cóclea/fisiopatologia , Modelos Animais de Doenças , Potenciais Evocados Auditivos do Tronco Encefálico , Feminino , Marcadores Genéticos , Predisposição Genética para Doença , Células Ciliadas Auditivas/metabolismo , Humanos , Masculino , Camundongos Endogâmicos C57BL , Pessoa de Meia-Idade , Fenótipo , Valor Preditivo dos Testes , Presbiacusia/sangue , Presbiacusia/fisiopatologia , Curva ROC , Reação em Cadeia da Polimerase em Tempo Real , Regulação para CimaRESUMO
Mutations in the GJB2 gene are known to represent the commonest cause of hereditary and congenital hearing loss. In this study, a complete sequencing of the GJB2 gene in a cohort of 506 patients from a single, large cochlear implant program in Europe was performed. Audiological testing for those patients who could actively participate was performed using pure tone audiometry (PTA). Those unable to undergo PTA were measured using click-auditory brainstem response (ABR). Data analysis was performed to determine genotype-phenotype correlations of the mutational status vs. audiological profiles and vs. age at the time of presentation. An overall prevalence of biallelic mutations of 13.4% was found for the total collective. When subsets of younger patients were examined, the prevalence increased to 27% of those up to age 18 and 35% of those up to age 5 at the time of testing, respectively. This increase was found to be highly significant (p < 0.001). Analysis of the mean PTA thresholds revealed a strong correlation between allele combination status and mean PTA (p = 0.021). The prevalence of simple heterozygotes was found to be approximately 10.1%, which is around 3.3 times the value expected in the general population. As GJB2 follows a recessive pattern of inheritance, the question arises as to why such a large fraction of simple heterozygotes was observed among the hearing impaired patients included in this study.
Assuntos
Conexinas/genética , Transtornos da Audição/genética , Audição/genética , Mutação , Estimulação Acústica , Adolescente , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Audiometria de Tons Puros , Limiar Auditivo , Criança , Pré-Escolar , Conexina 26 , Análise Mutacional de DNA , Potenciais Evocados Auditivos do Tronco Encefálico , Feminino , Frequência do Gene , Estudos de Associação Genética , Predisposição Genética para Doença , Alemanha/epidemiologia , Transtornos da Audição/diagnóstico , Transtornos da Audição/epidemiologia , Transtornos da Audição/fisiopatologia , Heterozigoto , Homozigoto , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Fenótipo , Prevalência , Estudos Retrospectivos , Fatores de Risco , Fatores Sexuais , Adulto JovemRESUMO
A cornerstone technique in the study of hearing is the Auditory Brainstem Response (ABR), an electrophysiologic technique that can be used as a quantitative measure of hearing function. Previous studies have published databases of baseline ABR thresholds for mouse strains, providing a valuable resource for the study of baseline hearing function and genetic mapping of hearing traits in mice. In this study, we further expand upon the existing literature by characterizing the baseline ABR characteristics of 100 inbred mouse strains, 47 of which are newly characterized for hearing function. We identify several distinct patterns of baseline hearing deficits and provide potential avenues for further investigation. Additionally, we characterize the sensitivity of the same 100 strains to noise exposure using permanent thresholds shifts, identifying several distinct patterns of noise-sensitivity. The resulting data provides a new resource for studying hearing loss and noise-sensitivity in mice.
Assuntos
Tronco Encefálico/fisiopatologia , Potenciais Evocados Auditivos do Tronco Encefálico , Perda Auditiva Provocada por Ruído/fisiopatologia , Audição , Ruído/efeitos adversos , Estimulação Acústica , Animais , Fadiga Auditiva , Modelos Animais de Doenças , Potenciais Evocados Auditivos do Tronco Encefálico/genética , Predisposição Genética para Doença , Audição/genética , Perda Auditiva Provocada por Ruído/genética , Testes Auditivos , Fenótipo , Especificidade da EspécieRESUMO
OBJECTIVE: Noise-induced hearing loss (NIHL) is a worldwide health problem and a growing concern among young people. Although some people appear to be more susceptible to NIHL, genetic association studies lack a specific phenotype. We tested the feasibility of a bilateral 4000-6000 Hz audiometric notch as a phenotype for identifying genetic contributions to hearing loss in young adults. DESIGN: A case-control-control study was conducted to examine selected SNPs in 52 genes previously associated with hearing loss and/or expressed in the cochlea. A notch was defined as a minimum of a 15-dB drop at 4000-6000 Hz from the previous best threshold with a 5-dB 'recovery' at 8000 Hz. STUDY SAMPLE: Participants were 252 individuals of European descent taken from a population of 640 young adults who are students of classical music. Participants were grouped as No-notch (NN), Unilateral Notch (UN), or Bilateral Notch (BN). RESULTS: The strongest evidence of a genetic association with the 4000-6000 Hz notch was a nonsynonymous SNP variant in the ESRR- gene (rs61742642:C> T, P386S). Carriers of the minor allele accounted for 26% of all bilateral losses. CONCLUSION: This study indicates that the 4000-6000 Hz bilateral notch is a feasible phenotype for identifying genetic susceptibility to hearing loss.
Assuntos
Audiometria/métodos , Perda Auditiva Provocada por Ruído/diagnóstico , Perda Auditiva Provocada por Ruído/genética , Audição/genética , Ruído/efeitos adversos , Polimorfismo de Nucleotídeo Único , Estimulação Acústica , Adolescente , Adulto , Limiar Auditivo , Estudos de Casos e Controles , Estudos de Viabilidade , Feminino , Frequência do Gene , Estudos de Associação Genética , Predisposição Genética para Doença , Perda Auditiva Provocada por Ruído/fisiopatologia , Humanos , Masculino , Fenótipo , Projetos Piloto , Valor Preditivo dos Testes , Fatores de Risco , Adulto JovemRESUMO
Kv1.1 subunits of low voltage-activated (Kv) potassium channels are encoded by the Kcna1 gene and crucially determine the synaptic integration window to control the number and temporal precision of action potentials in the auditory brainstem of mammals and birds. Prior electrophysiological studies showed that auditory signaling is compromised in monaural as well as in binaural neurons of the auditory brainstem in Kv1.1 knockout mice (Kcna1(-/-)). Here we examine the behavioral effects of Kcna1 deletion on sensory tasks dependent on either binaural processing (detecting the movement of a sound source across the azimuth), monaural processing (detecting a gap in noise), as well as binaural summation of the acoustic startle reflex (ASR). Hearing thresholds measured by auditory brainstem responses (ABR) do not differ between genotypes, but our data show a much stronger performance of wild type mice (+/+) in each test during binaural hearing which was lost by temporarily inducing a unilateral hearing loss (through short term blocking of one ear) thus remarkably, leaving no significant difference between binaural and monaural hearing in Kcna1(-/-) mice. These data suggest that the behavioral effect of Kv1.1 deletion is primarily to impede binaural integration and thus to mimic monaural hearing.
Assuntos
Percepção Auditiva , Comportamento Animal , Transtornos da Audição/metabolismo , Audição , Canal de Potássio Kv1.1/deficiência , Estimulação Acústica , Animais , Vias Auditivas/fisiopatologia , Percepção Auditiva/genética , Limiar Auditivo , Potenciais Evocados Auditivos do Tronco Encefálico , Feminino , Genótipo , Audição/genética , Transtornos da Audição/genética , Transtornos da Audição/fisiopatologia , Canal de Potássio Kv1.1/genética , Masculino , Camundongos Endogâmicos C3H , Camundongos Knockout , Fenótipo , Psicoacústica , Reflexo de Sobressalto , Detecção de Sinal Psicológico , Localização de Som , Fatores de TempoRESUMO
Ribbon synapses of cochlear inner hair cells (IHCs) employ efficient vesicle replenishment to indefatigably encode sound. In neurons, neuroendocrine and immune cells, vesicle replenishment depends on proteins of the mammalian uncoordinated 13 (Munc13, also known as Unc13) and Ca(2+)-dependent activator proteins for secretion (CAPS) families, which prime vesicles for exocytosis. Here, we tested whether Munc13 and CAPS proteins also regulate exocytosis in mouse IHCs by combining immunohistochemistry with auditory systems physiology and IHC patch-clamp recordings of exocytosis in mice lacking Munc13 and CAPS isoforms. Surprisingly, we did not detect Munc13 or CAPS proteins at IHC presynaptic active zones and found normal IHC exocytosis as well as auditory brainstem responses (ABRs) in Munc13 and CAPS deletion mutants. Instead, we show that otoferlin, a C2-domain protein that is crucial for vesicular fusion and replenishment in IHCs, clusters at the plasma membrane of the presynaptic active zone. Electron tomography of otoferlin-deficient IHC synapses revealed a reduction of short tethers holding vesicles at the active zone, which might be a structural correlate of impaired vesicle priming in otoferlin-deficient IHCs. We conclude that IHCs use an unconventional priming machinery that involves otoferlin.
Assuntos
Potenciais Evocados Auditivos do Tronco Encefálico/fisiologia , Células Ciliadas Auditivas Internas/metabolismo , Proteínas de Membrana/genética , Transmissão Sináptica/fisiologia , Vesículas Sinápticas/metabolismo , Animais , Proteínas de Ligação ao Cálcio/genética , Tomografia com Microscopia Eletrônica , Exocitose/fisiologia , Feminino , Células Ciliadas Auditivas Internas/citologia , Audição/genética , Audição/fisiologia , Peptídeos e Proteínas de Sinalização Intracelular/genética , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Proteínas do Tecido Nervoso/genética , Técnicas de Cultura de Órgãos , Técnicas de Patch-ClampRESUMO
Among the major distance senses of vertebrates, the ear is unique in its complex morphological changes during evolution. Conceivably, these changes enable the ear to adapt toward sensing various physically well-characterized stimuli. This review develops a scenario that integrates sensory cell with organ evolution. We propose that molecular and cellular evolution of the vertebrate hair cells occurred prior to the formation of the vertebrate ear. We previously proposed that the genes driving hair cell differentiation were aggregated in the otic region through developmental re-patterning that generated a unique vertebrate embryonic structure, the otic placode. In agreement with the presence of graviceptive receptors in many vertebrate outgroups, it is likely that the vertebrate ear originally functioned as a simple gravity-sensing organ. Based on the rare occurrence of angular acceleration receptors in vertebrate outgroups, we further propose that the canal system evolved with a more sophisticated ear morphogenesis. This evolving morphogenesis obviously turned the initial otocyst into a complex set of canals and recesses, harboring multiple sensory epithelia each adapted to the acquisition of a specific aspect of a given physical stimulus. As support for this evolutionary progression, we provide several details of the molecular basis of ear development.
Assuntos
Evolução Biológica , Orelha Interna , Células Ciliadas Auditivas , Morfogênese/genética , Vertebrados , Estimulação Acústica , Animais , Orelha Interna/anatomia & histologia , Orelha Interna/crescimento & desenvolvimento , Orelha Interna/fisiologia , Células Ciliadas Auditivas/citologia , Células Ciliadas Auditivas/fisiologia , Audição/genética , MutaçãoRESUMO
Since deafness is the most common sensorineural disorder in humans, better understanding of the underlying causes is necessary to improve counseling and rehabilitation. A Dutch family with autosomal dominantly inherited sensorineural hearing loss was clinically and genetically assessed. The MYO6 gene was selected to be sequenced because of similarities with other, previously described DFNA22 phenotypes and a pathogenic c.3610C > T (p.R1204W) mutation was found to co-segregate with the disease. This missense mutation results in a flat configured audiogram with a mild hearing loss, which becomes severe to profound and gently to steeply downsloping later in life. The age-related typical audiograms (ARTA) constructed for this family resemble presbyacusis. Speech audiometry and results of loudness scaling support the hypothesis that the phenotype of this specific MYO6 mutation mimics presbyacusis.
Assuntos
Perda Auditiva Neurossensorial/genética , Audição/genética , Mutação de Sentido Incorreto , Cadeias Pesadas de Miosina/genética , Presbiacusia/genética , Estimulação Acústica , Adolescente , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Audiometria de Tons Puros , Audiometria da Fala , Limiar Auditivo , Criança , Análise Mutacional de DNA , Progressão da Doença , Feminino , Predisposição Genética para Doença , Perda Auditiva Neurossensorial/fisiopatologia , Perda Auditiva Neurossensorial/psicologia , Hereditariedade , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Fenótipo , Presbiacusia/fisiopatologia , Presbiacusia/psicologia , Percepção da Fala , Vestíbulo do Labirinto/fisiopatologia , Adulto JovemRESUMO
OBJECTIVE: The purpose of this review was to evaluate the current literature on phosphoribosylpyrophosphate synthetase 1 (PRPS1)-related diseases and their consequences on hearing function. DESIGN: A literature search of peer-reviewed, published journal articles was conducted in online bibliographic databases. STUDY SAMPLE: Three databases for medical research were included in this review. RESULTS: Mutations in PRPS1 are associated with a spectrum of non-syndromic to syndromic hearing loss. Hearing loss in male patients with PRPS1 mutations is bilateral, moderate to profound, and can be prelingual or postlingual, progressive or non-progressive. Audiogram shapes associated with PRPS1 deafness are usually residual and flat. Female carriers can have unilateral or bilateral hearing impairment. Gain of function mutations in PRPS1 cause a superactivity of the PRS-I protein whereas the loss-of-function mutations result in X-linked nonsyndromic sensorineural deafness type 2 (DFN2), or in syndromic deafness including Arts syndrome and X-linked Charcot-Marie-Tooth disease-5 (CMTX5). CONCLUSIONS: Lower residual activity in PRS-I leads to a more severe clinical manifestation. Clinical and molecular findings suggest that the four PRPS1 disorders discovered to date belong to the same disease spectrum. Dietary supplementation with S-adenosylmethionine (SAM) appeared to alleviate the symptoms of Arts syndrome patients, suggesting that SAM could compensate for PRS-I deficiency.
Assuntos
Perda Auditiva/genética , Audição/genética , Mutação , Ribose-Fosfato Pirofosfoquinase/genética , Suplementos Nutricionais , Feminino , Predisposição Genética para Doença , Perda Auditiva/diagnóstico , Perda Auditiva/tratamento farmacológico , Perda Auditiva/enzimologia , Perda Auditiva/fisiopatologia , Hereditariedade , Humanos , Masculino , Fenótipo , S-Adenosilmetionina/uso terapêutico , Índice de Gravidade de Doença , Fatores SexuaisRESUMO
OBJECTIVE: To explore the molecular genetic characterization of two Chinese families with aminoglycoside-induced and non-syndromic hearing loss (NSHL). DESIGN: Clinical evaluations, sequence analysis of mitochondrial DNA (mtDNA) as well as two nuclear genes TRMU and MTO1 encoding mitochondrial proteins. STUDY SAMPLE: Two Chinese families with aminoglycoside-induced and NSHL. RESULTS: Clinical evaluations revealed incomplete penetrance (28.6% vs. 40.0%) and variable phenotype of hearing losses between two families. When the effect of aminoglycosides was excluded, the penetrances were both 0%. Sequence analysis of mitochondrial genomes showed a homoplasmic 1494C > T mutation in the12S rRNA gene (MT-RNR1) in all maternal relatives, as well as distinct sets of mtDNA polymorphism belonging to Eastern Asian haplogroups D4j and D5a2, respectively. However, none of these mtDNA variants was highly evolutionarily conserved and implicated to have functional significance. No mutations were identified in either TRMU or MTO1 gene. CONCLUSIONS: Mitochondrial 1494C> T mutation is the molecular basis responsible for the NSHL of two families, and the use of aminoglycoside antibiotics can worsen the hearing of the mutation carriers. Our results indicate the importance of a systematic screening for the mitochondrial 1494C > T mutation in Chinese subjects in the prevention of aminoglycoside-induced and non-syndromic hearing loss.
Assuntos
Aminoglicosídeos/efeitos adversos , Antibacterianos/efeitos adversos , Povo Asiático/genética , DNA Mitocondrial/genética , Perda Auditiva/induzido quimicamente , Perda Auditiva/genética , Audição , Mutação , RNA Ribossômico/genética , Estimulação Acústica , Adulto , Audiometria , Limiar Auditivo , Proteínas de Transporte/genética , Criança , Pré-Escolar , China/epidemiologia , Análise Mutacional de DNA , Feminino , Predisposição Genética para Doença , Haplótipos , Audição/efeitos dos fármacos , Audição/genética , Perda Auditiva/etnologia , Perda Auditiva/fisiopatologia , Hereditariedade , Humanos , Masculino , Proteínas Mitocondriais/genética , Linhagem , Penetrância , Proteínas de Ligação a RNA , tRNA Metiltransferases/genéticaRESUMO
This study describes the heritability of audiometric shape parameters and the familial aggregation of different types of presbycusis in a healthy, otologically screened population between 50 and 75 years old. About 342 siblings of 64 families (average family-size: 5.3) were recruited through population registries. Audiometric shape was mathematically quantified by objective parameters developed to measure size, slope, concavity, percentage of frequency-dependent and frequency-independent hearing loss and Bulge Depth. The heritability of each parameter was calculated using a variance components model. Logistic regression models were used to estimate the odds ratios (ORs). Estimates of sibling recurrence risk ratios (lambda(s)) are also provided. Heritability estimates were generally higher compared to previous studies. ORs and lambda(s) for the parameters Total Hearing Loss (size), Uniform Hearing Loss (percentage of frequency-dependent hearing loss) and Bulge Depth suggest a higher heredity for severe types of presbycusis compared to moderate or mild types. Our results suggest that the separation of the parameter 'Total Hearing Loss' into the two parameters 'Uniform Hearing Loss' and 'Non-uniform Hearing Loss' could lead to the discovery of different genetic subtypes of presbycusis. The parameter 'Bulge Depth', instead of 'Concavity', seemed to be an important parameter for classifying subjects into 'susceptible' or 'resistant' to societal or intensive environmental exposure.
Assuntos
Audição/genética , Presbiacusia/genética , Estimulação Acústica , Fatores Etários , Idoso , Audiometria , Limiar Auditivo , Bélgica , Condução Óssea/genética , Feminino , Predisposição Genética para Doença , Hereditariedade , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Modelos Biológicos , Razão de Chances , Linhagem , Fenótipo , Presbiacusia/diagnóstico , Presbiacusia/fisiopatologia , Medição de Risco , Fatores de Risco , Índice de Gravidade de Doença , Fatores Sexuais , IrmãosRESUMO
The neural cell adhesion molecule (NCAM) plays important roles in development of the nervous system and in synaptic plasticity and memory formation in the adult. The present study sought to further investigate the role of NCAM in learning by testing habituation and footshock sensitization learning of the startle response (SR) in NCAM null mutant (NCAM-/-) and wildtype littermate (NCAM+/+) mice. Whereas habituation is a form of non-associative learning, footshock sensitization is induced by rapid contextual fear conditioning. Habituation was tested by repetitive presentation of acoustic and tactile startle stimuli. Although NCAM-/- mice showed differences in sensitivity in both stimulus modalities, habituation learning was intact in NCAM-/- mice, suggesting that NCAM does not play a role in the mechanisms underlying synaptic plasticity in the startle pathway. Footshock sensitization was elicited by presentation of electric footshocks between two series of acoustic stimuli. In contrast to habituation, footshock sensitization learning was attenuated in NCAM-/- mice: the acoustic SR increase after the footshocks was lower in the mutant than in wildtype mice, indicating that NCAM plays an important role in the relevant brain areas, such as amygdala and/or the hippocampus.
Assuntos
Aprendizagem por Associação/fisiologia , Habituação Psicofisiológica/fisiologia , Moléculas de Adesão de Célula Nervosa/fisiologia , Reflexo de Sobressalto/fisiologia , Estimulação Acústica , Animais , Limiar Auditivo/fisiologia , Condicionamento Operante/fisiologia , Feminino , Habituação Psicofisiológica/genética , Audição/genética , Audição/fisiologia , Camundongos , Camundongos Knockout , Moléculas de Adesão de Célula Nervosa/genética , Plasticidade Neuronal/genética , Plasticidade Neuronal/fisiologia , Reflexo de Sobressalto/genética , Tato/genética , Tato/fisiologiaRESUMO
Acid-base homeostasis of endolymph is thought to be essential for normal inner ear function. This assumption was supported by clinical data from individuals affected by autosomal recessive distal renal tubular acidosis with sensorineural hearing loss. This recessive syndrome was recently demonstrated to be due to mutations in the gene encoding the B1 subunit of H(+)-ATPase (ATP6B1). To examine the potential roles of H(+)-ATPase B1 subunit in inner ear development and function, we defined its spatial and temporal expression patterns in the developing mouse inner ear and examined the morphologic and physiologic effects of loss of its function. Standard in situ hybridization was used for the expression study with routine morphologic and physiologic assessments of hearing and balance in H(+)-ATPase B1 subunit (Atp6b1) null mutant mice. Atp6b1 mRNA was first detected at embryonic day 11.5 (E11.5) in the endolymphatic duct epithelia. From E16.5 onward, Atp6b1 was also observed in the presumptive interdental cell layer of the spiral limbus in the cochlea. Auditory brainstem response tests revealed normal hearing in mice lacking Atp6b1. The inner ears of these mice develop normally and show no overt morphological abnormalities. Our data demonstrate that Atp6b1 is not critical for normal inner ear development or normal inner ear function in mice and suggest that other proton-transporting mechanisms or pH buffering systems must allow the mouse inner ear to compensate for lack of normal Atp6b1 activity.
Assuntos
Audição/fisiologia , Subunidades Proteicas/fisiologia , ATPases Vacuolares Próton-Translocadoras/fisiologia , Estimulação Acústica , Animais , Animais Recém-Nascidos , Limiar Auditivo , Cóclea/embriologia , Orelha Interna/patologia , Embrião de Mamíferos/metabolismo , Desenvolvimento Embrionário e Fetal , Potenciais Evocados Auditivos do Tronco Encefálico , Feminino , Audição/genética , Hibridização In Situ , Masculino , Camundongos , Camundongos Knockout , Subunidades Proteicas/genética , Distribuição Tecidual , ATPases Vacuolares Próton-Translocadoras/genéticaRESUMO
The multi-subunit H+-ATPase pump is present at particularly high density on the apical (luminal) surface of -intercalated cells of the cortical collecting duct of the distal nephron, where vectorial proton transport is required for urinary acidification. The complete subunit composition of the apical ATPase, however, has not been fully agreed upon. Functional failure of -intercalated cells results in a group of disorders, the distal renal tubular acidoses (dRTA), whose features include metabolic acidosis accompanied by disturbances of potassium balance, urinary calcium solubility, bone physiology and growth. Mutations in the gene encoding the B-subunit of the apical pump (ATP6B1) cause dRTA accompanied by deafness. We previously localized a gene for dRTA with preserved hearing to 7q33-34 (ref. 4). We report here the identification of this gene, ATP6N1B, which encodes an 840 amino acid novel kidney-specific isoform of ATP6N1A, the 116-kD non-catalytic accessory subunit of the proton pump. Northern-blot analysis demonstrated ATP6N1B expression in kidney but not other main organs. Immunofluorescence studies in human kidney cortex revealed that ATP6N1B localizes almost exclusively to the apical surface of -intercalated cells. We screened nine dRTA kindreds with normal audiometry that linked to the ATP6N1B locus, and identified different homozygous mutations in ATP6N1B in eight. These include nonsense, deletion and splice-site changes, all of which will truncate the protein. Our findings identify a new kidney-specific proton pump 116-kD accessory subunit that is highly expressed in proton-secreting cells in the distal nephron, and illustrate its essential role in normal vectorial acid transport into the urine by the kidney.
Assuntos
Acidose Tubular Renal/genética , Audição/genética , Mutação , Proteínas da Gravidez , Bombas de Próton/química , Bombas de Próton/genética , ATPases Translocadoras de Prótons , Fatores Supressores Imunológicos , Acidose Tubular Renal/metabolismo , Acidose Tubular Renal/urina , Adenosina Trifosfatases/genética , Adenosina Trifosfatases/metabolismo , Adolescente , Adulto , Sequência de Aminoácidos , Audiometria , Northern Blotting , Encéfalo/metabolismo , Criança , Pré-Escolar , Cromossomos Humanos Par 7 , Mapeamento de Sequências Contíguas , DNA Complementar/metabolismo , Éxons , Feminino , Deleção de Genes , Genes Recessivos , Ligação Genética , Marcadores Genéticos , Audição/fisiologia , Homozigoto , Humanos , Rim/metabolismo , Rim/patologia , Córtex Renal/metabolismo , Masculino , Microscopia de Fluorescência , ATPases Mitocondriais Próton-Translocadoras , Modelos Genéticos , Dados de Sequência Molecular , Linhagem , Mapeamento Físico do Cromossomo , Polimorfismo Genético , Polimorfismo Conformacional de Fita Simples , Biossíntese de Proteínas , Isoformas de Proteínas , Bombas de Próton/biossíntese , Splicing de RNA , Recombinação Genética , Homologia de Sequência de Aminoácidos , Distribuição Tecidual , ATPases Vacuolares Próton-TranslocadorasRESUMO
We used a combination of subtractive hybridization and differential screening strategies to identify genes that may function normally in hearing and, when mutated, result in deafness. A human fetal cochlear (membranous labyrinth) cDNA library was subtracted against total human fetal brain RNAs by an avidin-biotin-based procedure to enrich for cochlear transcripts. Subtracted cochlear clones were differentially screened with 32P-labeled total cochlear and total brain cDNA probes. Sequence analysis of clones that hybridized more intensely with cochlear than with brain cDNA probes revealed some previously characterized genes, including mitochondrial sequences, collagen type I alpha-2 (COL1A2), collagen type II alpha-1 (COL2A1), collagen type III alpha-1 (COL3A1), spermidine/spermine N1-acetyltransferase (SAT), osteonectin (SPARC), and peripheral myelin protein 22 (PMP22). Also identified were clones that are potential novel cochlear genes. Northern blots of cochlear and brain RNAs probed with COL1A2, COL2A1, COL3A1, SAT, SPARC, PMP22, and a novel sequence, designated Coch-5B2, confirm results of the subtractive procedure by showing preferential cochlear expression. A number of these genes serve structural or regulatory functions in extracellular matrix or neural conduction; defects in some of these genes are associated with disorders involving hearing loss. Partial sequence analysis of Coch-5B2 reveals a von Willebrand factor type A-like domain in this cDNA. To assess the cochlear specificity of Coch-5B2, a Northern blot panel of 14 human fetal tissue RNAs was probed with Coch-5B2, showing differential expression of this novel gene in the cochlea.