NeuroD-null mice are deaf due to a severe loss of the inner ear sensory neurons during development

  • Kim WY; 
  • Fritzsch B; 
  • Serls A; 
  • Bakel LA; 
  • Huang EJ; 
  • 외 3명
Citations

WEB OF SCIENCE

271
Citations

SCOPUS

292

초록

A key factor in the genetically programmed development of the nervous system is the death of massive numbers of neurons. Therefore, genetic mechanisms governing cell survival are of fundamental importance to developmental neuroscience. We report that inner ear sensory neurons are dependent on a basic helix-loop-helix transcription factor called NeuroD for survival during differentiation. Mice lacking NeuroD protein exhibit no auditory evoked potentials, reflecting a profound deafness. DiI fiber staining, immunostaining and cell death assays reveal that the deafness is due to the failure of inner ear sensory neuron survival during development. The affected inner ear sensory neurons fail to express neurotrophin receptors, TrkB and T-kC, suggesting that the ability of NeuroD to support neuronal survival may be directly mediated through regulation of responsiveness to the neurotrophins.

키워드

basic helix-loop-helix protein; NeuroD; inner ear; cell death; TrkC; TrkB; deafness; mouse; AUDITORY EVOKED-POTENTIALS; HAIR-CELLS; FUNCTIONAL-ANATOMY; EXPRESSION; GENE; DIFFERENTIATION; ECTODERM; CORTEX; TRKB; RAT
제목
NeuroD-null mice are deaf due to a severe loss of the inner ear sensory neurons during development
저자
Kim WY; Fritzsch B; Serls A; Bakel LA; Huang EJ; Reichardt LF; Barth DS; Lee JE
DOI
10.1242/dev.128.3.417
발행일
2001-02
저널명
Development (Cambridge)
권
128
호
3
페이지
417 ~ 426