UVA Scientists Discover Process for Fixing Damaged Hearing Cells

University of Virginia School of Medicine researchers have discovered how cells that let us hear can repair themselves after being damaged, an insight that could benefit efforts to treat and prevent hearing loss.

“Hair cells” found in the inner ear are important both for the ability to hear and for a sense of balance. They are known as hair cells because they are covered in hair-like structures that serve as mechanical antennas for sound detection. When auditory hair cells are killed, they are gone for good, but the new UVA Health research shows these delicate cells can repair themselves from damage caused by loud noises or other forms of stress.

For many years, research has focused on regeneration of sensory hair cells. Although those efforts continue, it is equally important to better understand the mechanisms that govern repair and maintenance of the cells, said researcher Jung-Bum Shin, of UVA’s Department of Neuroscience.

“By gaining a deeper understanding of these inherent repair processes, we can uncover strategies to fortify them effectively,” Shin said.

One future approach may use drugs to stimulate cell repair, he said.

“When replacement of hair cells proves challenging, the focus shifts toward repairing them instead. This dual strategy of regeneration and repair holds strong potential in advancing treatments for hearing loss and associated conditions,” Shin said.

Hearing Repair

Hair cells are naturally fragile. They must be delicate so they can sense sound, but they must also withstand the continuous mechanical stress inherent in their jobs.

Researcher Jung-Bum Shin, of UVA’s Department of Neuroscience, says the discovery could lead to hearing loss treatments that involve stimulating the nerves to repair themselves. (Photo by Dan Addison, University Communications)

Prolonged exposure to loud noise harms hair cells in a variety of ways, and one of those is by damaging the cores of the “hairs” themselves. These hair-like structures are known as stereocilia, and Shin’s new research shows a process they use to repair themselves.

The hair cells deploy a protein called XIRP2, which can sense damage to the cores that are made of a substance called actin. Shin and his team found that XIRP2 first senses damage, then migrates to the damage site and repairs the cores by filling in new actin.

This process is also relevant to the broader study of cell biology, Shin said.

The pioneering work netted Shin and his colleagues more than $2.3 million from the National Institutes of Health (grant R01DC021176) to fund additional research into how the cores are repaired. By understanding this, scientists will be better positioned to develop new ways to battle hearing loss – even loss due to aging, the researchers say.

“Age-related hearing loss affects at least a third of all older adults,” Shin said. “Understanding and harnessing internal mechanisms by which hair cells counteract wear and tear will be crucial in identifying ways to prevent age-related hearing loss. Furthermore, this knowledge holds potential implications for associated conditions such as Alzheimer’s disease and other dementia conditions.”

Findings Published

The researchers published their findings in the scientific journal eLife. The article is open access, meaning it is free to read.

The research team consisted of Elizabeth L. Wagner, Jun-Sub Im, Stefano Sala, Maura I. Nakahata, Terence E. Imbery, Sihan Li, Daniel Chen, Katherine Nimchuk, Yael Noy, David W. Archer, Wenhao Xu, George Hashisaki, Karen B. Avraham, Patrick W. Oakes and Shin. The researchers have no financial interest in the work.

The research was supported by the National Institutes of Health’s National Institute on Deafness and Other Communication Disorders, grants R01DC014254, R56DC017724, R01DC018842, R01DC011835 and 1F31DC017370-01. Additional support was provided by the Owens Family Foundation, the Virginia Lions Hearing Foundation, and a National Science Foundation CAREER Award.

Article originally appeared on UVA Today