The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing.
Christian VoglTanvi ButolaNatja HaagTorben J HausratMichael G LeitnerMichel MoutschenPhilippe P LefèbvreCarsten SpeckmannLillian GarrettLore BeckerHelmut FuchsMartin Hrabe de AngelisSandor NietzscheMichael M KesselsDominik OliverMatthias KneusselManfred W KilimannNicola StrenzkePublished in: EMBO reports (2017)
Lipopolysaccharide-responsive beige-like anchor protein (LRBA) belongs to the enigmatic class of BEACH domain-containing proteins, which have been attributed various cellular functions, typically involving intracellular protein and membrane transport processes. Here, we show that LRBA deficiency in mice leads to progressive sensorineural hearing loss. In LRBA knockout mice, inner and outer hair cell stereociliary bundles initially develop normally, but then partially degenerate during the second postnatal week. LRBA deficiency is associated with a reduced abundance of radixin and Nherf2, two adaptor proteins, which are important for the mechanical stability of the basal taper region of stereocilia. Our data suggest that due to the loss of structural integrity of the central parts of the hair bundle, the hair cell receptor potential is reduced, resulting in a loss of cochlear sensitivity and functional loss of the fraction of spiral ganglion neurons with low spontaneous firing rates. Clinical data obtained from two human patients with protein-truncating nonsense or frameshift mutations suggest that LRBA deficiency may likewise cause syndromic sensorineural hearing impairment in humans, albeit less severe than in our mouse model.
Keyphrases
- hearing loss
- protein protein
- mouse model
- single cell
- binding protein
- amino acid
- endothelial cells
- electronic health record
- induced apoptosis
- cell therapy
- preterm infants
- replacement therapy
- inflammatory response
- multiple sclerosis
- toll like receptor
- type diabetes
- randomized controlled trial
- small molecule
- risk assessment
- spinal cord injury
- drug delivery
- intellectual disability
- immune response
- adipose tissue
- skeletal muscle
- lps induced
- artificial intelligence
- signaling pathway
- mesenchymal stem cells
- study protocol
- wastewater treatment