MUC2 expression in human middle ear epithelium of patients with otitis media

被引:22
作者
Ubell, Matthew L. [1 ]
Kerschner, Joseph E. [1 ]
Wackym, P. Ashley [1 ,2 ]
Burrows, Amy [1 ]
机构
[1] Med Coll Wisconsin, Div Pediat Otolaryngol, Dept Otolaryngol & Commun Sci, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Div Otol & Neurootol Skull Base Surg, Milwaukee, WI 53226 USA
关键词
D O I
10.1001/archoto.2007.10
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: To compare levels of expression of mucin gene 2 (MUC2), a major secretory mucin, in the middle ear of patients with otitis media (OM) and control patients. Design: Case-control study. Setting: Children's Hospital of Wisconsin, Milwaukee. Patients: Nineteen patients aged 6 months to 15 years undergoing routine ventilation tube insertion for recurrent OM or chronic OM with effusion and 8 controls with no history of OM undergoing cochlear implantation. Interventions: Biopsy of middle ear epithelium for RNA extraction. Main Outcome Measure: Expression of MUC2 by real-time reverse transcription-polymerase chain reaction. Results: Twenty-seven OM samples (17 recurrent and 10 with effusion) from 19 patients were analyzed and compared with 9 control samples from 8 patients. The mean MUC2 expression was 6.12 (95% confidence interval, 3.32-8.89) times that of the controls in the OM samples overall, 5.00 (95% confidence interval, 2.79-7.21) times that of controls in the recurrent OM samples, and 7.98 (95% confidence interval, 1.58-14.38) times that of controls in the OM with effusion samples. Conclusions: Levels of MUC2 expression in human middle ear epithelium are significantly increased in patients with OM overall, patients with recurrent OM, and patients with OM with effusion compared with controls. Mucins are fundamentally important in the middle ear, controlling viscoelastic properties of secretions and providing mucosal protection and bacterial clearance. Demonstration of these differences between patient groups highlights the need for greater understanding of molecular responses in OM, which may provide novel interventions for this common problem.
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页码:39 / 44
页数:6
相关论文
共 19 条
[1]   Polymorphism of the human TNF-α promoter -: random variation or functional diversity? [J].
Allen, RD .
MOLECULAR IMMUNOLOGY, 1999, 36 (15-16) :1017-1027
[2]  
BLUESTONE CD, 1996, PEDIAT OTOLARYNGOLOG, V1, P388
[3]  
BROWN DT, 1985, ARCH OTOLARYNGOL, V111, P688
[4]   The innate immune response of the respiratory epithelium [J].
Diamond, G ;
Legarda, D ;
Ryan, LK .
IMMUNOLOGICAL REVIEWS, 2000, 173 :27-38
[5]   Mucosal biofilm formation on middle-ear mucosa in the chinchilla model of otitis media [J].
Ehrlich, GD ;
Veeh, R ;
Wang, X ;
Costerton, JW ;
Hayes, JD ;
Hu, FZ ;
Daigle, BJ ;
Ehrlich, MD ;
Post, JC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (13) :1710-1715
[6]   Direct detection of bacterial Biofilms on the middle-ear mucosa of children with chronic otitis media [J].
Hall-Stoodley, Luanne ;
Hu, Fen Ze ;
Gieseke, Armin ;
Nistico, Laura ;
Nguyen, Duc ;
Hayes, Jay ;
Forbes, Michael ;
Greenberg, David P. ;
Dice, Bethany ;
Burrows, Amy ;
Wackym, P. Ashley ;
Stoodley, Paul ;
Post, J. Christopher ;
Ehrlich, Garth D. ;
Kerschner, Joseph E. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 296 (02) :202-211
[7]   Promoter analysis and aberrant expression of the MUC5B gene in diffuse panbronchiolitis [J].
Kamio, K ;
Matsushita, I ;
Hijikata, M ;
Kobashi, Y ;
Tanaka, G ;
Nakata, K ;
Ishida, T ;
Tokunaga, K ;
Taguchi, Y ;
Homma, S ;
Nakata, K ;
Azuma, A ;
Kudoh, S ;
Keicho, N .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (09) :949-957
[8]   Signaling pathways in interleukin-1β-mediated middle ear mucin secretion [J].
Kerschner, JE ;
Yang, C ;
Burrows, A ;
Cioffi, JA .
LARYNGOSCOPE, 2006, 116 (02) :207-211
[9]   Chinchilla middle ear epithelial mucin gene expression in response to inflammatory cytokines [J].
Kerschner, JE ;
Meyer, TK ;
Burrows, A .
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2004, 130 (10) :1163-1167
[10]   Middle ear epithelial mucin production in response to interleukin-6 exposure in vitro [J].
Kerschner, JE ;
Meyer, TK ;
Yang, C ;
Burrows, A .
CYTOKINE, 2004, 26 (01) :30-36