A research team from Nanjing University has used cochlear organoids to identify drugs that can promote the regeneration of hair cells. The study, published in Stem Cell Reports, also identifies a signaling pathway as a potential target for hearing restoration.
The resulting vibrations are transmitted to the ossicles comprising a chain of three small bones called malleus, incus and stape located within the middle ear. Movement of the bones transmits the sound vibrations to the inner ear, sending a signal to the cochlea (a hollow spiraling structure filled with fluid). Vibrations cause the fluid within the cochlea to ripple, forming waves that stimulate the movement of hair cells positioned on the top of the basilar membrane that separates the two fluid-filled chambers running along the cochlea.
Cochlea hair cells are tuned to respond to various pitches of sound: those positioned at the widest part of the cochlea detect higher-pitched sounds whereas the cells located towards the center detect lower-pitched sounds. The hairs generate an electrical signal that is carried by the auditory nerve to the brain converting it to a sound that we can recognize.
While birds and amphibians are able to regenerate lost hair cells, this isnt the case for mammalian cochlea hair cells they cannot be repaired or replaced, and so their destruction results in hearing loss. In the cochlea, hair cells are surrounded by a group of supporting cells, which share common ancestors as the hair cells and are less vulnerable to damage, says Wan.
He notes that current efforts to treat hearing loss have been directed to induce conversion or reprogramming of these supporting cells to produce functional hair cells: Some of the known reprogramming signals include Notch inhibition, Wnt activation and expression of transcription factors such as Atoh1 or Pou4f3. However, it is likely that additional mechanisms are involved in efficient regeneration of mature and functional hair cells.
Wan explains that the key benefit to using organoids, compared to two-dimensional cultures, is that they can faithfully recapture some of the key inner ear development processes and are able to differentiate into hair cells with remarkable structural and functional similarities to the native hair cells.
The organoids were used to screen a library of US Food and Drug Administration (FDA)-approved drugs to determine if any were able to stimulate the formation of hair cells. The high-throughput screen identified an anti-cancer drug called regorafenib that could do just that.
Regorafenib is a clinically-approved drug for the treatment of gastrointestinal tumors. It works by suppressing the formation of new blood vessels required by tumors. Interestingly, in our study, regorafenib promotes hair cell regeneration in a different mechanism, whereby it inhibits the production of an anti-differentiation molecule TGFB1. It is a fine example of how unbiased screening can uncover new drugs with previously unrecognized effects, says Wan.
Until now, according to Wan, a key obstacle to the large-scale screening of modulators for hair cell regeneration was the lack of a high-throughput mammalian hair cell culture platform. Wan elaborates, We believe that the development and application of cochlear organoids, along with recent advances in multiomics and gene editing tools, should greatly move this area forward.
Several further studies are ongoing in the laboratory. As for regorafenib, the researchers are currently investigating its hair cell-inducing effects in vivo in preclinical rodent models. We are also expanding the drug library to identify new molecules and signaling pathways for differentiation and maturation of hair cells.
Lastly and importantly, the cochlear organoid system enables us to perform multiomics and large-scale gene editing studies to uncover secrets in the development and regeneration of mammalian hair cells, concludes Wan.Reference: Lui Q, Zhang L, Zhu M-S, Wan G. High-throughput screening on cochlear organoids identifies VEGFR-MEKTGFB1 signaling promoting hair cell reprogramming. Stem Cell Rep. 2021;16:1-17. doi: 10.1016/j.stemcr.2021.08.010Guoqiang Wan was speaking with Laura Elizabeth Lansdowne, Managing Editor for Technology Networks.
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