4.5 Article

A Novel in vitro Model Delineating Hair Cell Regeneration and Neural Reinnervation in Adult Mouse Cochlea

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnmol.2021.757831

关键词

hair cell; adult; regeneration; novel model; cochlea

资金

  1. NIH [R01DC006908, R56DC006908, UG3TR002636]
  2. DOD [W81XWH1810331]
  3. Fredrick and Ines Yeatts hair cell regeneration fellowship
  4. David-Shulsky Foundation
  5. National Key R&D Program of China [2017YFA0103900]
  6. National Science Foundation for outstanding young people [81922018]
  7. National Natural Science Foundation of China [81771011]
  8. Key Laboratory of Hearing Medicine, National Health and Family Planning Commission, Shanghai, China
  9. U.S. Department of Defense (DOD) [W81XWH1810331] Funding Source: U.S. Department of Defense (DOD)

向作者/读者索取更多资源

The study describes a culture system for adult mammalian auditory system that overcomes the limitations posed by the tough bone encasement of the inner ear. The researchers use intact cochlear structures to maintain overall inner ear architecture and improve sensor epithelium survival in culture. They show successful transdifferentiation of adult supporting cells into hair cell-like cells and demonstrate their ability to attract adult ganglion neurites. The culture system holds potential for diverse studies including regeneration, hair cell-neuron pathways, and inner ear drug screening.
The study of an adult mammalian auditory system, such as regeneration, has been hampered by the lack of an in vitro system in which hypotheses can be tested efficiently. This is primarily due to the fact that the adult inner ear is encased in the toughest bone of the body, whereas its removal leads to the death of the sensory epithelium in culture. We hypothesized that we could take advantage of the integral cochlear structure to maintain the overall inner ear architecture and improve sensory epithelium survival in culture. We showed that by culturing adult mouse cochlea with the (surrounding) bone intact, the supporting cells (SCs) survived and almost all hair cells (HCs) degenerated. To evaluate the utility of the explant culture system, we demonstrated that the overexpression of Atoh1, an HC fate-determining factor, is sufficient to induce transdifferentiation of adult SCs to HC-like cells (HCLCs). Transdifferentiation-derived HCLCs resemble developmentally young HCs and are able to attract adult ganglion neurites. Furthermore, using a damage model, we showed that degenerated adult ganglions respond to regenerated HCLCs by directional neurite outgrowth that leads to HCLC-neuron contacts, strongly supporting the intrinsic properties of the HCLCs in establishing HCLC-neuron connections. The adult whole cochlear explant culture is suitable for diverse studies of the adult inner ear including regeneration, HC-neuron pathways, and inner ear drug screening.

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