Health / Health News

    Protein involved in hearing loss recovery

    The snail-shaped cochlea is an organ in the inner ear that helps us to hear sounds. Within the cochlea, thousands of sensory cells known as hair cells are arranged in inner and outer rows. Vibrations from sound waves cause these hair cells to move up and down and create an electrical signal that travels to the brain. Long or repeated exposure to loud noises can damage and even destroy hair cells. This noise-induced hearing loss can be permanent.



    Loud and long-lasting sounds can damage sensitive structures in the inner ear.


    A team led by Dr. Patricia White of the University of Rochester previously showed that a protein called Forkhead Box O3 (FOXO3) is expressed in both inner and outer hair cells.

    FOXO3 is a transcription factor—a type of protein that plays a role in gene regulation. Upon noise exposure, FOXO3 travels into the hair cell nucleus, suggesting it might play a role in the protective response to noise-induced damage. To test this hypothesis, the scientists used mice that had been genetically modified to lack the gene for FOXO3.

    The scientists first explored the effect of noise on hearing. One day afterward, the researchers found that the mice lacking FOXO3 had become profoundly deaf.

    The mice with FOXO3 also had hearing loss, but it was far less severe. Two weeks afterward, the mice lacking FOXO3 continued to have severe hearing loss, but the normal mice seemed to mostly recover their hearing.

    The team examined the effect of noise on structural damage to hair cells and other parts of the cochlea. They found that FOXO3 is needed for outer hair cell survival after loud noise.

    They linked the hearing loss in the FOXO3-deficient mice with outer hair cell loss and structural damage. Inner hair cells survived and appeared to be relatively undamaged. Finally, the scientists found FOXO3 in cochlear hair cells from a human cadaver, supporting the idea that it may also play a role in human hearing. (NIH)

    MAY 13, 2017



    YOU MAY ALSO LIKE

    Scientists have identified differences in a group of genes they say might help explain why some people need a lot more sleep — and others less — than most.
    If the standard supplementation of 400 IUs of vitamin D is increased to 800 IUs daily there are reductions in the number of premature and preterm babies with extremely low bone density.
    A connection between common household chemicals and birth defects has been uncovered by new research.
    Brazil ranks tenth for preterm birth, with approximately 300 thousand premature babies every year—11.7% of the total births in the country. Most cases stem from teenage or late pregnancies, precarious prenatal care, or illnesses afflicting the mother.
    Traumatic head injury can have widespread effects in the brain, but now scientists can look in real time at how head injury affects thousands of individual cells and genes simultaneously in mice.
    In a study of four patients with a rare genetic disorder, researchers found that PIEZO2, a gene previously shown to control our sense of our bodies in space and gentle touch, may also be responsible for tactile allodynia: the skin’s reaction to injury that makes normally gentle touches feel painful.

    © 1991-2023 The Titi Tudorancea Bulletin | Titi Tudorancea® is a Registered Trademark | Terms of use and privacy policy
    Contact