Association between human beta defensin expression and cholesteatoma formation

Auris Nasus Larynx. 2006 Jun;33(2):159-65. doi: 10.1016/j.anl.2005.11.023. Epub 2006 Jan 23.

Abstract

Objective: To investigate an association between human beta defensin (hBD) expression and cholesteatoma formation.

Methods: hBD-2 mRNA expressions were assessed in healthy external acoustic meatus skin organ cultures before and after stimulation with Pseudomonas aeruginosa. In addition, hBD-1 and hBD-2 protein production of stimulated and non-stimulated external acoustic meatus skin was visualized by immunohistochemistry. Furthermore, hBD-1 and hBD-2 mRNA expression was analyzed in 25 external acoustic meatus skin, 29 cholesteatoma, and 18 non-cholesteatoma control samples. Non-stimulated meatal tissue preparation did not express hBD-2, whereas incubation with P. aeruginosa demonstrated hBD-2 induction.

Results: The hBD-1 mRNA expression was detected in cholesteatoma (14/17), meatal skin, and middle ear mucosa (11/18). hBD-2 mRNA expression was shown in eight cholesteatoma (28.5%) and in three middle ear mucosa tissue samples (37.5%).

Conclusion: Our data suggest constitutional hBD-1 and inducible hBD-2 expression in chronic middle ear infection and cholesteatoma. Failure of hBD-1 and hBD-2 expression might dispose to exacerbation of cholesteatoma disease. The organ culture model of the external acoustic meatus skin is effective in order to evaluate germ stimulation experiments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Child
  • Child, Preschool
  • Cholesteatoma, Middle Ear / genetics*
  • Cholesteatoma, Middle Ear / metabolism*
  • Cholesteatoma, Middle Ear / pathology
  • DNA Primers / genetics
  • DNA Primers / metabolism
  • DNA, Complementary / genetics
  • DNA, Complementary / metabolism
  • Defensins / genetics*
  • Defensins / metabolism*
  • Disease Progression
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mucous Membrane / metabolism
  • Polymerase Chain Reaction
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcription / genetics

Substances

  • DNA Primers
  • DNA, Complementary
  • Defensins
  • RNA, Messenger