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Experience-dependent flexibility in a molecularly diverse central-to-peripheral auditory feedback system.
Frank, Michelle M; Sitko, Austen A; Suthakar, Kirupa; Torres Cadenas, Lester; Hunt, Mackenzie; Yuk, Mary Caroline; Weisz, Catherine J C; Goodrich, Lisa V.
Afiliação
  • Frank MM; Department of Neurobiology, Harvard Medical School, Boston, United States.
  • Sitko AA; Department of Neurobiology, Harvard Medical School, Boston, United States.
  • Suthakar K; Section on Neuronal Circuitry, National Institute on Deafness and Other Communication Disorders, Bethesda, United States.
  • Torres Cadenas L; Section on Neuronal Circuitry, National Institute on Deafness and Other Communication Disorders, Bethesda, United States.
  • Hunt M; Department of Neurobiology, Harvard Medical School, Boston, United States.
  • Yuk MC; Department of Neurobiology, Harvard Medical School, Boston, United States.
  • Weisz CJC; Section on Neuronal Circuitry, National Institute on Deafness and Other Communication Disorders, Bethesda, United States.
  • Goodrich LV; Department of Neurobiology, Harvard Medical School, Boston, United States.
Elife ; 122023 03 06.
Article em En | MEDLINE | ID: mdl-36876911
Just as our pupils dilate or shrink depending on the amount of light available to our eyes, our ears adjust their sensitivity based on the sound environment we encounter. Evidence suggests that a group of cells known as olivocochlear neurons (OCNs for short) may be involved in this process. These cells are located in the brainstem but project into the cochlea, the inner ear structure that converts sound waves into the electrical impulses relayed to the brain. OCNs may mediate how sounds are detected and encoded "at the source." Historically, OCNs have been divided into two groups (medial or lateral OCNs) based on different morphologies and roles in hearing. For instance, medial OCNs are thought to protect our ears against loud sounds by sending molecular signals to the inner ear cells that amplify certain auditory signals. However, it remains difficult to disentangle the precise function of the different types of OCNs, in part because scientists still lack markers that would allow them to distinguish between medial and lateral cells simply based on genetic activity. Frank et al. aimed to eliminate this bottleneck by identifying which genes were switched on and to what degree in individual mouse medial and lateral OCNs; this was done throughout development and after exposure to loud noises. The experiments uncovered a range of genetic markers for medial and lateral OCNs, showing that these cells switch on different sets of genes relevant to their role over development. This gene expression data also revealed that two distinct groups of lateral OCNs exist, one of which is characterised by the production of large amounts of neuropeptides, a type of chemical messenger that can modulate neural circuit activity. Further work in both developing and adult mice showed that this production is shaped by the activity of the cells, with the neuropeptide levels increasing when the animals are exposed to damaging levels of noise. This change lasts for several days, suggesting that such an experience can have long-lasting effects on how the brain provides feedback to the ear. Overall, the results by Frank et al. will help to better identify and characterize the different types of OCNs and the role that they have in hearing. By uncovering the chemical messengers that mediate the response to loud noises, this research may contribute to a better understanding of how to prevent or reduce hearing loss.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Núcleo Olivar / Perda Auditiva Provocada por Ruído Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Núcleo Olivar / Perda Auditiva Provocada por Ruído Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article