Indispensable role of Mdm2/p53 interaction during the embryonic and postnatal inner ear development

M Laos1, M Sulg1, A Herranen1

  • 1Division of Physiology and Neuroscience, Department of Biosciences, University of Helsinki, 00014 Helsinki, Finland.

Scientific Reports
|February 10, 2017
PubMed

Insights

Excess p53 protein, regulated by Mdm2, is lethal to developing auditory cells. Maturation reduces sensitivity, but postmitotic cells remain vulnerable, potentially explaining auditory issues in developmental syndromes.

Area of Science:

  • Cellular biology
  • Developmental biology
  • Genetics

Background:

  • p53 is crucial for cellular stress response.
  • Mdm2 negatively regulates p53 levels.
  • The role of balanced p53 in normal tissue development is unclear.

Purpose of the Study:

  • Investigate the in vivo effects of Mdm2/p53 interaction disruption.
  • Analyze the impact on early-embryonic otic progenitor cells and their auditory descendants.
  • Determine if p53 restricts auditory supporting cell regeneration.

Main Methods:

  • Studied Mdm2 abrogation in vivo.
  • Examined otic progenitor cells, auditory supporting cells, and hair cells.
  • Investigated p53's role in supporting cell proliferation and transdifferentiation in vitro.

Main Results:

  • p53 accumulation due to Mdm2 abrogation proved lethal to both proliferative and differentiating otic cells.
  • Sensitivity of postmitotic supporting cells to excess p53 decreased with maturation.
  • p53 inactivation did not affect supporting cell proliferative quiescence or transdifferentiation capacity in vitro.

Conclusions:

  • Developing hair and supporting cells lack protection against p53 upregulation.
  • Maturation-related mechanisms may limit p53's pro-apoptotic activity.
  • Findings may link p53 dysregulation to auditory disturbances in developmental syndromes.