Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease

Proc Natl Acad Sci U S A. 2024 Dec 3;121(49):e2322124121. doi: 10.1073/pnas.2322124121. Epub 2024 Nov 25.

Abstract

Variants in the gene NDP cause Norrie disease, a severe dual-sensory disorder characterized by congenital blindness due to disrupted retinal vascular development and progressive hearing loss accompanied by sensory hair cell death. NDP encodes the secreted signaling molecule norrin. The role of norrin in the cochlea is incompletely understood. We investigated whether the Norrie disease cochlear pathology can be ameliorated in an Ndp-knockout (Ndp-KO) mouse model by conditional activation of stabilized β-catenin in vascular endothelial cells. We hypothesized that in the cochlea microvasculature, β-catenin is the primary downstream intracellular effector of norrin binding to endothelial cell surface receptors and that restoration of this signaling pathway is sufficient to prevent sensory hair cell death and hearing loss. We show that tamoxifen induction of Cdh5CreERT2;Ctnnb1flex3/+;Ndp-KO mice stabilizing β-catenin in vascular endothelial cells alone rescued defects in cochlear vascular barrier function, restored dysregulated expression of endothelial cell disease biomarkers (Cldn5, Abcb1a, Slc7a1, and Slc7a5), and prevented progressive outer hair cell death and hearing loss. Single-cell transcriptome profiling of human cochleas showed NDP expression by fibrocytes and glial cells while receptor gene expression (FZD4, TSPAN12, LRP5, and LRP6) coincided in vascular endothelial cells. Our findings support the conclusion that vascular endothelial cells are a primary target of norrin signaling in the cochlea of mice and humans and restoration of β-catenin regulation of target gene expression within cochlear endothelial cells is sufficient to maintain a cochlear microenvironment critical for hair cell survival.

Keywords: NDP; cochlea; norrin; vascular endothelial cells.

MeSH terms

  • Animals
  • Blindness / congenital
  • Blindness / genetics
  • Blindness / metabolism
  • Blindness / pathology
  • Blindness / prevention & control
  • Cochlea* / blood supply
  • Cochlea* / metabolism
  • Cochlea* / pathology
  • Disease Models, Animal
  • Endothelial Cells / metabolism
  • Eye Proteins / genetics
  • Eye Proteins / metabolism
  • Genetic Diseases, X-Linked / genetics
  • Genetic Diseases, X-Linked / metabolism
  • Genetic Diseases, X-Linked / pathology
  • Hair Cells, Auditory* / metabolism
  • Hair Cells, Auditory* / pathology
  • Hearing Loss, Sensorineural* / genetics
  • Hearing Loss, Sensorineural* / metabolism
  • Hearing Loss, Sensorineural* / pathology
  • Humans
  • Mice
  • Mice, Knockout*
  • Nerve Tissue Proteins* / genetics
  • Nerve Tissue Proteins* / metabolism
  • Nervous System Diseases
  • Retinal Degeneration / genetics
  • Retinal Degeneration / metabolism
  • Retinal Degeneration / pathology
  • Retinal Degeneration / prevention & control
  • Signal Transduction
  • Spasms, Infantile* / genetics
  • Spasms, Infantile* / metabolism
  • Spasms, Infantile* / pathology
  • beta Catenin* / genetics
  • beta Catenin* / metabolism

Substances

  • beta Catenin
  • Ndph protein, mouse
  • Nerve Tissue Proteins
  • Eye Proteins
  • CTNNB1 protein, mouse

Supplementary concepts

  • Norrie disease