King's College London

A new King’s-led study, published in The Proceedings of the National Academy of Sciences, has found that a single factor (a protein coding gene known as Sox8) can make non-ear cells adopt ear character during embryo development. The findings not only demonstrate how cell fate decisions are regulated in the embryo but may also inform reprogramming and regenerative strategies for the ear developmental malformations. 

Responsible for the sense of hearing and balance, the inner ear is critically important for communication with the environment. In humans, developmental malformations of the ear have life-long consequences, while age-related hearing defects affect a large proportion of the population. Currently, there are no therapies that involve biological approaches – only hearing aids or cochlear implants, as how the ear normally develops is not fully understood and many of the controlling factors are poorly characterised.

Researchers from the Faculty of Dentistry, Oral and Craniofacial Sciences at King’s, in collaboration with colleagues from the Francis Crick Institute, explored the earliest steps in ear development to determine what causes cells to become ear cells, and what makes them different from cells which form other sense organs.

The adult inner ear has a very complex anatomy. It contains many different cell types such as sensory hair cells, which receive sound and balance information from the outside world and transform it into an electrical signal that is transmitted to the brain by neurons of the cochlear-vestibular ganglion. Supporting cells help the hair cells in their role, while other cells are specialised to ensure the right composition of inner ear fluids.

Despite this complexity, during embryo development the ear develops from a simple sheet of cells that first make a vesicle, which is then gradually transformed into the adult structure. While this happens, different cell types differentiate at the right place and time. This incredibly complicated and requires coordination of many different processes.

Using a combination of different methods ranging from embryological approaches to state-of-the-art molecular methods the King’s team identified a single factor that initiates the ear program: the transcription factor Sox8. Transcription factors regulate other genes to make sure that they are expressed in the desired cells at the right time and in the right amount throughout the life of the cell and the organism.

Expressing Sox8 in non-ear cells that normally generate other sense organs makes them to form vesicles that look like ear vesicles and have a genetic make-up similar to normal ear vesicles. More surprisingly, they can be found not just near the normal ear, but all over the head and generate neurons like the normal ear. This is a key finding as it is the first time that a factor not only induced the morphological changes that happen during normal ear formation, but also activates the programme to produce specialised cell types in the ear: the neurons.

Future research will need to identify how Sox8 works, and whether it works alone or with co-factors. The authors hope this will lead to a pathway towards reprogramming other cells into ear cells and inform regenerative strategy for ear developmental malformations.

‘Sox8 remodels the cranial ectoderm to generate the ear’ (DOI: 10.1073/pnas.2118938119) (Ailin Leticia Buzzi, Jingchen Chen, Alexandre Thiery, Julien Delile, & Andrea Streit) was published in The Proceedings of the National Academy of Sciences.