Počet záznamů: 1  

Early Deletion of Neurod1 Alters Neuronal Lineage Potential and Diminishes Neurogenesis in the Inner Ear

  1. 1.
    SYSNO ASEP0556361
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevEarly Deletion of Neurod1 Alters Neuronal Lineage Potential and Diminishes Neurogenesis in the Inner Ear
    Tvůrce(i) Filova, Iva (BTO-N) ORCID
    Bohuslavová, Romana (BTO-N) RID
    Tavakoli, Mitra (BTO-N)
    Yamoah, E. (US)
    Fritzsch, B. (US)
    Pavlínková, Gabriela (BTO-N) RID, ORCID
    Celkový počet autorů6
    Číslo článku845461
    Zdroj.dok.Frontiers in Cell and Developmental Biology. - : Frontiers Research Foundation - ISSN 2296-634X
    Roč. 10, FEB 17 2022 (2022)
    Poč.str.16 s.
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovanull mice ; sensory epithelia ; auditory-system ; hair-cells ; transcription
    Vědní obor RIVEB - Genetika a molekulární biologie
    Obor OECDDevelopmental biology
    CEPGA20-06927S GA ČR - Grantová agentura ČR
    LM2018126 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    LM2018129 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    EF18_046/0016045 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Způsob publikováníOpen access
    Institucionální podporaBTO-N - RVO:86652036
    UT WOS000771905600001
    EID SCOPUS85125859391
    DOI10.3389/fcell.2022.845461
    AnotaceNeuronal development in the inner ear is initiated by expression of the proneural basic Helix-Loop-Helix (bHLH) transcription factor Neurogenin1 that specifies neuronal precursors in the otocyst. The initial specification of the neuroblasts within the otic epithelium is followed by the expression of an additional bHLH factor, Neurod1. Although NEUROD1 is essential for inner ear neuronal development, the different aspects of the temporal and spatial requirements of NEUROD1 for the inner ear and, mainly, for auditory neuron development are not fully understood. In this study, using Foxg1(Cre) for the early elimination of Neurod1 in the mouse otocyst, we showed that Neurod1 deletion results in a massive reduction of differentiating neurons in the otic ganglion at E10.5, and in the diminished vestibular and rudimental spiral ganglia at E13.5. Attenuated neuronal development was associated with reduced and disorganized sensory epithelia, formation of ectopic hair cells, and the shortened cochlea in the inner ear. Central projections of inner ear neurons with conditional Neurod1 deletion are reduced, unsegregated, disorganized, and interconnecting the vestibular and auditory systems. In line with decreased afferent input from auditory neurons, the volume of cochlear nuclei was reduced by 60% in Neurod1 mutant mice. Finally, our data demonstrate that early elimination of Neurod1 affects the neuronal lineage potential and alters the generation of inner ear neurons and cochlear afferents with a profound effect on the first auditory nuclei, the cochlear nuclei.
    PracovištěBiotechnologický ústav
    KontaktMonika Kopřivová, Monika.Koprivova@ibt.cas.cz, Tel.: 325 873 700
    Rok sběru2023
    Elektronická adresahttps://www.frontiersin.org/articles/10.3389/fcell.2022.845461/full
Počet záznamů: 1  

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