microRNA‑183 is involved in the differentiation and regeneration of Notch signaling‑prohibited hair cells from mouse cochlea

Zhou,Wei; Du,Jintao; Jiang,Di; Wang,Xianren; Chen,Kaitian; Tang,Haocheng; Zhang,Xuemei; Cao,Hui; Zong,Ling; Dong,Chang; Jiang,Hongyan

doi:10.3892/mmr.2018.9127

August-2018 Volume 18 Issue 2

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August-2018 Volume 18 Issue 2

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Article Open Access

microRNA‑183 is involved in the differentiation and regeneration of Notch signaling‑prohibited hair cells from mouse cochlea

Authors:
- Wei Zhou
- Jintao Du
- Di Jiang
- Xianren Wang
- Kaitian Chen
- Haocheng Tang
- Xuemei Zhang
- Hui Cao
- Ling Zong
- Chang Dong
- Hongyan Jiang
View Affiliations / Copyright

Affiliations: Department of Otolaryngology, The First Affiliated Hospital and Institute of Otorhinolaryngology, Sun Yat‑sen University, Guangzhou, Guangdong 510080, P.R. China

Copyright: © Zhou et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Pages: 1253-1262
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Published online on: June 5, 2018

https://doi.org/10.3892/mmr.2018.9127
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Abstract

Auditory hair cell regeneration following injury is critical to hearing restoration. The Notch signaling pathway participates in the regulation of inner ear development and cell differentiation. Recent evidence suggests that microRNA (miR)‑183 has a similar role in the inner ear. However, it is unclear how Notch signaling functions in hair cell regeneration in mammals and if there is cross‑talk between Notch signaling and miR‑183. The present study used a gentamicin‑induced cochlear injury mouse model. Gentamicin‑induced damage of the hair cells activated the Notch signaling pathway and downregulated miR‑183 expression. Notch signaling inhibition by the γ‑secretase inhibitor, 24‑diamino‑5‑phenylthiazole (DAPT), attenuated gentamicin‑induced hair cell loss and reversed the downregulation of miR‑183 expression. Further investigation revealed that the novel hair cells produced, induced by DAPT, were derived from transdifferentiated supporting cells. Additionally, myosin VI‑positive hair cell numbers were increased by Notch signaling inhibition in in vitro experiments with cultured neonatal mouse inner ear precursor cells. This effect was reversed by miR‑183 inhibition. These findings indicate that the Notch signaling pathway served a repressing role during the regeneration of hair cells. Inhibiting this signal improved hair cell regeneration in the gentamicin‑damaged cochlear model. miR‑183 was demonstrated to be involved in hair cell differentiation and regeneration, and was required for the differentiation of the Notch‑inhibited hair cells.

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Journals

International Journal of Molecular Medicine

International Journal of Oncology

Molecular Medicine Reports

Oncology Reports

Experimental and Therapeutic Medicine

Oncology Letters

Biomedical Reports

Molecular and Clinical Oncology

World Academy of Sciences Journal

International Journal of Functional Nutrition

International Journal of Epigenetics

Medicine International

microRNA‑183 is involved in the differentiation and regeneration of Notch signaling‑prohibited hair cells from mouse cochlea

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