PTEN attenuates PIP3/Akt signaling in the cochlea of the aging CBA/J mouse

Hear Res. 2010 Jun 1;264(1-2):86-92. doi: 10.1016/j.heares.2009.09.002. Epub 2009 Sep 15.


We have previously reported the activation of cell death pathways in the sensory cells of the aging cochlea. Here we investigate age-associated changes in survival mechanisms focusing on phosphatidylinositol 3,4,5-trisphosphate (PIP(3))/Akt signaling. The animal model is the CBA/J mouse of 18 months of age prior to the onset of major functional loss (ABR thresholds, 26+/-8 dB SPL) which is compared to young animals of 3 months of age (ABR thresholds, 19+/-7 dB SPL). Immunostaining on cochlear cryosections revealed a wide-spread distribution of PIP(3) in the cochlea which was markedly attenuated in old animals in inner and outer hair cells, Deiters cells and pillar cells. Protein levels of the lipid phosphatase PTEN which regulates PIP(3) increased in those cells with aging while its mRNA did not, suggesting an age-related reduction of PTEN degradation. Furthermore, staining intensity of phosphorylated PTEN (ser380) and its nuclear localization increased. Consistent with a reduction of PIP(3), the phosphorylation of the downstream target Akt at threonine 308 significantly decreased in outer hair cells. The results suggest a decline of the survival capacity of aging outer hair cells due to a decrease in PIP(3)/Akt signaling caused by an increase of PTEN.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acoustic Stimulation
  • Age Factors
  • Aging / metabolism*
  • Aging / pathology
  • Animals
  • Auditory Threshold
  • Blotting, Western
  • Cell Survival
  • Cochlea / metabolism*
  • Cochlea / pathology
  • Hair Cells, Auditory, Outer / metabolism
  • Hair Cells, Auditory, Outer / pathology
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Inbred CBA
  • PTEN Phosphohydrolase / genetics
  • PTEN Phosphohydrolase / metabolism*
  • Phosphatidylinositol Phosphates / metabolism*
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / metabolism*
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction*
  • Threonine


  • Phosphatidylinositol Phosphates
  • RNA, Messenger
  • phosphatidylinositol 3,4,5-triphosphate
  • Threonine
  • Proto-Oncogene Proteins c-akt
  • PTEN Phosphohydrolase
  • Pten protein, mouse