GJB2 gene mutations are the most common causes of autosomal recessive non-syndromic hereditary deafness.For individuals suffering from severe to profound GJB2-related deafness,cochlear implants have emerged as the sol...GJB2 gene mutations are the most common causes of autosomal recessive non-syndromic hereditary deafness.For individuals suffering from severe to profound GJB2-related deafness,cochlear implants have emerged as the sole remedy for auditory improvement.Some previous studies have highlighted the crucial role of preserving cochlear neural components in achieving favorable outcomes after cochlear implantation.Thus,we generated a conditional knockout mouse model(Cx26-CKO)in which Cx26 was completely deleted in the cochlear supporting cells driven by the Sox2 promoter.The Cx26-CKO mice showed severe hearing loss and massive loss of hair cells and Deiter’s cells,which represented the extreme form of human deafness caused by GJB2 gene mutations.In addition,multiple pathological changes in the peripheral auditory nervous system were found,including abnormal innervation,demyelination,and degeneration of spiral ganglion neurons as well as disruption of heminodes in Cx26-CKO mice.These findings provide invaluable insights into the deafness mechanism and the treatment for severe deafness in Cx26-null mice.展开更多
基金supported by the National Key Research and Development Program of China(2021YFF0702303)the National Natural Science Foundation of China(82301324,82301323,and 82071058).
文摘GJB2 gene mutations are the most common causes of autosomal recessive non-syndromic hereditary deafness.For individuals suffering from severe to profound GJB2-related deafness,cochlear implants have emerged as the sole remedy for auditory improvement.Some previous studies have highlighted the crucial role of preserving cochlear neural components in achieving favorable outcomes after cochlear implantation.Thus,we generated a conditional knockout mouse model(Cx26-CKO)in which Cx26 was completely deleted in the cochlear supporting cells driven by the Sox2 promoter.The Cx26-CKO mice showed severe hearing loss and massive loss of hair cells and Deiter’s cells,which represented the extreme form of human deafness caused by GJB2 gene mutations.In addition,multiple pathological changes in the peripheral auditory nervous system were found,including abnormal innervation,demyelination,and degeneration of spiral ganglion neurons as well as disruption of heminodes in Cx26-CKO mice.These findings provide invaluable insights into the deafness mechanism and the treatment for severe deafness in Cx26-null mice.
