Modulation of Mcl-1 expression reduces age-related cochlear degeneration

Neurobiol Aging. 2013 Nov;34(11):2647-58. doi: 10.1016/j.neurobiolaging.2013.05.012. Epub 2013 Jun 19.

Abstract

Mcl-1 is an anti-apoptotic member of the Bcl-2 family that modulates apoptosis-related signaling pathways and promotes cell survival. We have previously demonstrated a reduction of Mcl-1 expression in aging cochleae. To investigate whether restoring Mcl-1 expression would reduce aging-related cochlear degeneration, we developed a rat model of Mcl-1 overexpression. A plasmid encoding human Mcl-1/enhanced green fluorescent protein was applied to the round window of the cochlea. This in vivo treatment transfected both the sensory and supporting cells of the cochlear sensory epithelium and enhanced Mcl-1 expression at both the mRNA and the protein level. The upregulation of Mcl-1 expression reduced the progression of age-related cochlear dysfunction and sensory cell death. Furthermore, the transfection of Mcl-1 exerted its protective effect by suppressing cochlear apoptosis at the mitochondrial level. This study demonstrates that the genetic modulation of Mcl-1 expression reduces the progression of age-related cochlear degeneration.

Keywords: Aging; Cochlea; Gene delivery; Hair cells; Intervention; Mcl-1; Rat.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / metabolism*
  • Age Factors
  • Aging / metabolism
  • Aging / pathology*
  • Animals
  • Apoptosis / genetics
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism*
  • Cochlea / metabolism*
  • Cochlea / pathology*
  • Copper-Transporting ATPases
  • Epithelium / metabolism
  • Epithelium / pathology
  • Evoked Potentials, Auditory, Brain Stem / physiology
  • Female
  • Green Fluorescent Proteins / genetics
  • Humans
  • In Vitro Techniques
  • Male
  • Nerve Degeneration / metabolism
  • Nerve Degeneration / pathology*
  • Rats
  • Rats, Inbred F344
  • Rats, Sprague-Dawley
  • Sensory Receptor Cells / metabolism
  • Sensory Receptor Cells / pathology*
  • Transfection
  • Up-Regulation / genetics

Substances

  • Cation Transport Proteins
  • Green Fluorescent Proteins
  • Adenosine Triphosphatases
  • ATP7A protein, human
  • Copper-Transporting ATPases