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Neurod1 Is Essential for the Primary Tonotopic Organization and Related Auditory Information Processing in the Midbrain
I. Macova, K. Pysanenko, T. Chumak, M. Dvorakova, R. Bohuslavova, J. Syka, B. Fritzsch, G. Pavlinkova,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
R01 AG060504
NIA NIH HHS - United States
NLK
Free Medical Journals
od 1981 do Před 6 měsíci
PubMed Central
od 1981 do Před 6 měsíci
Europe PubMed Central
od 1981 do Před 6 měsíci
Open Access Digital Library
od 1981-01-01
Open Access Digital Library
od 1981-01-01
- MeSH
- chování zvířat fyziologie MeSH
- colliculus inferior anatomie a histologie fyziologie MeSH
- ganglion spirale cytologie fyziologie MeSH
- mapování mozku MeSH
- mezencefalon embryologie fyziologie MeSH
- myši knockoutované MeSH
- myši MeSH
- nucleus cochlearis anatomie a histologie fyziologie MeSH
- sluch fyziologie MeSH
- sluchová percepce genetika fyziologie MeSH
- těhotenství MeSH
- transkripční faktory bHLH genetika fyziologie MeSH
- úleková reakce genetika fyziologie MeSH
- vestibulární aparát anatomie a histologie fyziologie MeSH
- vnímání výšky zvuku fyziologie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
Hearing depends on extracting frequency, intensity, and temporal properties from sound to generate an auditory map for acoustical signal processing. How physiology intersects with molecular specification to fine tune the developing properties of the auditory system that enable these aspects remains unclear. We made a novel conditional deletion model that eliminates the transcription factor NEUROD1 exclusively in the ear. These mice (both sexes) develop a truncated frequency range with no neuroanatomically recognizable mapping of spiral ganglion neurons onto distinct locations in the cochlea nor a cochleotopic map presenting topographically discrete projections to the cochlear nuclei. The disorganized primary cochleotopic map alters tuning properties of the inferior colliculus units, which display abnormal frequency, intensity, and temporal sound coding. At the behavioral level, animals show alterations in the acoustic startle response, consistent with altered neuroanatomical and physiological properties. We demonstrate that absence of the primary afferent topology during embryonic development leads to dysfunctional tonotopy of the auditory system. Such effects have never been investigated in other sensory systems because of the lack of comparable single gene mutation models.SIGNIFICANCE STATEMENT All sensory systems form a topographical map of neuronal projections from peripheral sensory organs to the brain. Neuronal projections in the auditory pathway are cochleotopically organized, providing a tonotopic map of sound frequencies. Primary sensory maps typically arise by molecular cues, requiring physiological refinements. Past work has demonstrated physiologic plasticity in many senses without ever molecularly undoing the specific mapping of an entire primary sensory projection. We genetically manipulated primary auditory neurons to generate a scrambled cochleotopic projection. Eliminating tonotopic representation to auditory nuclei demonstrates the inability of physiological processes to restore a tonotopic presentation of sound in the midbrain. Our data provide the first insights into the limits of physiology-mediated brainstem plasticity during the development of the auditory system.
Department of Biology University of Iowa Iowa City Iowa 52242 and
Citace poskytuje Crossref.org
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