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|    Can hearing loss be reversed? Research r    |
|    13 Feb 23 21:30:36    |
      MSGID: 1:317/3 63eb0e6e       PID: hpt/lnx 1.9.0-cur 2019-01-08       TID: hpt/lnx 1.9.0-cur 2019-01-08        Can hearing loss be reversed? Research reveals clues that could regrow       the cells that help us hear                Date:        February 13, 2023        Source:        University of Rochester Medical Center        Summary:        The most common cause of hearing loss is progressive because        hair cells - - the primary cells to detect sound waves -- cannot        regenerate if damaged or lost. Researchers are now getting closer        to identifying the mechanisms that may promote this type of        regeneration in mammals.                      Facebook Twitter Pinterest LinkedIN Email       FULL STORY       ==========================================================================       Taking a bite of an apple is considered a healthy choice. But have you       ever thought about putting in earplugs before your favorite band takes       the stage?              ==========================================================================       Just like your future body will thank you for the apple, your future ears       (specifically your cochlear hair cells) will thank you for protecting       them. The most common cause of hearing loss is progressive because       these hair cells - - the primary cells to detect sound waves -- cannot       regenerate if damaged or lost. People who have repeated exposure to loud       noises, like military personnel, construction workers, and musicians,       are most at risk for this type of hearing loss. But, it can happen to       anyone over time (even concert goers).              On the other hand, birds and fish can regenerate these hair cells,       and now researchers at the Del Monte Institute for Neuroscience are       getting closer to identifying the mechanisms that may promote this type       of regeneration in mammals, as explained in research recently published       in Frontiers in Cellular Neuroscience.              "We know from our previous work that expression of an active growth       gene, called ERBB2, was able to activate the growth of new hair cells       (in mammals), but we didn't fully understand why," said Patricia White,       PhD, professor of Neuroscience and Otolaryngology at the University of       Rochester Medical Center.              The 2018 study led by Jingyuan Zhang, PhD, a postdoctoral fellow in the       White lab at the time, found that activating the growth gene ERBB2 pathway       triggered a cascading series of cellular events by which cochlear support       cells began to multiply and activate other neighboring stem cells to       become new sensory hair cells.              "This new study tells us how that activation is happening -- a significant       advance toward the ultimate goal of generating new cochlear hair cells       in mammals," said White.              Using single-cell RNA sequencing in mice, researchers compared cells with       an overactive growth gene (ERBB2 signaling) with similar cells that lacked       such signaling. They found the growth gene -- ERBB2 -- promoted stem       cell-like development by initiating the expression of multiple proteins       -- including SPP1, a protein that signals through the CD44 receptor. The       CD44 receptor is known to be present in cochlear-supporting cells. This       increase in cellular response promoted mitosis in the supporting cells,       a key event for regeneration.              "When we checked this process in adult mice, we were able to show       that ERBB2 expression drove the protein expression of SPP1 that is       necessary to activate CD44 and grow new hair cells," said Dorota       Piekna-Przybylska, PhD, a staff scientist in the White Lab and first       author of the study. "This discovery has made it clear that regeneration       is not only restricted to the early stages of development. We believe       we can use these findings to drive regeneration in adults." "We plan to       further investigation of this phenomenon from a mechanistic perspective       to determine whether it can improve auditory function after damage in       mammals. That is the ultimate goal," said White.              Additional authors include Daxiang Na, Cameron Baker, and John Ashton,       PhD, at the University of Rochester and Medical Center. The research       was supported by the U.S. Army Medical Research Mechanism, the National       Institute on Deafness and Other Communication Disorders, UR Ventures,       and the Schmitt Program on Integrative Neuroscience.               * RELATED_TOPICS        o Health_&_Medicine        # Stem_Cells # Hearing_Loss # Immune_System # Hair_Loss        o Mind_&_Brain        # Hearing_Impairment # Neuroscience # Dementia #        Perception        * RELATED_TERMS        o Adult_stem_cell o Hearing_impairment o Hair o Healing o        Somatic_cell o Baldness o Stem_cell o Pernicious_anemia              ==========================================================================       Story Source: Materials provided by       University_of_Rochester_Medical_Center. Original written by Kelsie Smith       Hayduk. Note: Content may be edited for style and length.                     ==========================================================================       Journal Reference:        1. Dorota Piekna-Przybylska, Daxiang Na, Jingyuan Zhang, Cameron        Baker, John        M. Ashton, Patricia M. White. Single cell RNA sequencing analysis        of mouse cochlear supporting cell transcriptomes with activated        ERBB2 receptor indicates a cell-specific response that promotes        CD44 activation. Frontiers in Cellular Neuroscience, 2023; 16 DOI:        10.3389/ fncel.2022.1096872       ==========================================================================              Link to news story:       https://www.sciencedaily.com/releases/2023/02/230213201054.htm              --- up 50 weeks, 10 hours, 50 minutes        * Origin: -=> Castle Rock BBS <=- Now Husky HPT Powered! (1:317/3)       SEEN-BY: 15/0 106/201 114/705 123/120 153/7715 226/30 227/114 229/110       SEEN-BY: 229/111 112 113 114 307 317 400 426 428 470 664 700 292/854       SEEN-BY: 298/25 305/3 317/3 320/219 396/45       PATH: 317/3 229/426           |
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