論文

国際誌
2016年

Activation of NLRP3 inflammasome in human middle ear cholesteatoma and chronic otitis media.

Acta oto-laryngologica
  • Shin Kariya
  • ,
  • Mitsuhiro Okano
  • ,
  • Pengfei Zhao
  • ,
  • Yuko Kataoka
  • ,
  • Junko Yoshinobu
  • ,
  • Yukihide Maeda
  • ,
  • Hisashi Ishihara
  • ,
  • Takaya Higaki
  • ,
  • Kazunori Nishizaki

136
2
開始ページ
136
終了ページ
40
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.3109/00016489.2015.1093171

CONCLUSIONS: The nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) inflammasome plays an important role in the pathogenesis of middle ear diseases. Modulation of inflammasome-mediated inflammation may be a novel therapeutic strategy for cholesteatoma and chronic otitis media. OBJECTIVE: NLRP3 inflammasome is a critical molecule mediating interleukin (IL)-1β responses. However, the expression of NLRP3 in the pathogenesis of cholesteatoma and chronic otitis media has not been fully examined. This study sought to assess the expression of NLRP3, ASC (apoptosis-associated speck-like protein containing a caspase recruitment domain and a pyrin domain), and caspase-1 in middle ear tissues in patients with cholesteatoma or chronic otitis media. METHODS: Middle ear tissue samples were obtained from patients with cholesteatoma or chronic otitis media. Control middle ear samples were collected during cochlear implant surgery of patients without middle ear inflammation. The expression of NLRP3, ASC, and caspase-1 were examined by reverse transcription polymerase chain reaction (RT-PCR) assay and immunohistochemical study. RESULTS: The levels of mRNA of NLRP3, ASC, and caspase-1 were significantly elevated in cholesteatoma and chronic otitis media as compared with that of normal controls. The proteins of NLRP3, ASC, and caspase-1 were observed in infiltrating inflammatory cells in cholesteatoma and chronic otitis media.

リンク情報
DOI
https://doi.org/10.3109/00016489.2015.1093171
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/26457439
ID情報
  • DOI : 10.3109/00016489.2015.1093171
  • PubMed ID : 26457439

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