Mucin gene expression in human middle ear epithelium

被引:69
作者
Kerschner, Joseph Edward [1 ]
机构
[1] Med Coll Wisconsin, Childrens Hosp Wisconsin, Dept Otolaryngol & Commun Sci, Div Pediat Otolaryngol, Milwaukee, WI 53226 USA
关键词
mucin gene; human middle ear epithelium; otitis media;
D O I
10.1097/MLG.0b013e31806db531
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives: To investigate the expression of recently identified human mucin genes in human middle ear epithelial (MEE) specimens from in vivo middle ear (ME) tissue and to compare this mucin gene. expression with mucin gene expression in an immortalized cell culture in vitro source of human MEE. Methods: Human MEE was harvested as in vivo specimens, and human MEE cell cultures were established for in vitro experimentation. RNA was extracted from MEE and primers designed for reverse-transcription polymerase chain reaction to assess for mucin gene MUC1, MUC2, MUC3, MUC4, MUC5AC, MUC5B, MUC6, MUC7, MUC8, MUC9, MUC11, MUC12, MUC13, MUC15, MUC16, MUC18, MUC19, and MUC20 expression. Mucin gene expression in the in vivo and in vitro ME tissue was compared against tissues with known expression of the mucin genes in question. Results: Mucin genes MUC1, MUC2, MUC3, MUC4, MUC5AC, MUC5B, MUC7, MUC8, MUC9, MUC11, MUC13, MUC15, MUC16, MUC18, MUC19, and MUC20 were identified and expressed in both the in vivo and in vitro samples of MEE. Mucin genes MUC6, MUC12, and MUC17 were not identified in either tissue samples. Conclusion: Many of the mucin genes that have been recently identified are expressed in human MEE. These genes are expressed in a similar manner in both in vivo and in vitro models. Understanding the mechanisms in which these genes regulate the physiology and pathophysiology of MEE will provide a more thorough understanding of the molecular mechanics of the MEE and disease conditions such as otitis media.
引用
收藏
页码:1666 / 1676
页数:11
相关论文
共 49 条
[1]  
Ars B., 1997, Acta Oto-Rhino-Laryngologica Belgica, V51, P181
[2]  
Ball SS, 1997, ANN OTO RHINOL LARYN, V106, P633
[3]  
BLUESTONE CD, 1996, PEDIAT OTOLARYNGOLOG, P388
[4]   MUC7 20-mer: Investigation of antimicrobial activity, secondary structure, and possible mechanism of antifungal action [J].
Bobek, LA ;
Situ, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (02) :643-652
[5]  
BOBEK LA, 1993, J BIOL CHEM, V268, P20563
[6]   Effect of nitric oxide donation on mucin production in vitro [J].
Capper, R ;
Guo, L ;
Pearson, JP ;
Birchall, JP .
CLINICAL OTOLARYNGOLOGY, 2003, 28 (01) :51-54
[7]   OTITIS-MEDIA WITH EFFUSION - COMPONENTS WHICH CONTRIBUTE TO THE VISCOUS PROPERTIES [J].
CARRIE, S ;
HUTTON, DA ;
BIRCHALL, JP ;
GREEN, GGR ;
PEARSON, JP .
ACTA OTO-LARYNGOLOGICA, 1992, 112 (03) :504-511
[8]   Genome-wide search and identification of a novel gel-forming mucin MUC19/Muc19 in glandular tissues [J].
Chen, Y ;
Zhao, YH ;
Kalaslavadi, TB ;
Halmati, E ;
Nehrke, K ;
Le, AD ;
Ann, DK ;
Wu, R .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2004, 30 (02) :155-165
[9]   IL-1β promotes the ciliogenesis of human middle ear epithelial cells:: Possible linkage with the expression of mucin gene 8 [J].
Choi, JY ;
Kim, JY ;
Kim, CW ;
Ho, JS ;
Lee, KD ;
Yoo, JB ;
Ahn, YE ;
Yoon, JH .
ACTA OTO-LARYNGOLOGICA, 2005, 125 (03) :260-265
[10]  
Chonmaitree T, 1996, ANN OTO RHINOL LARYN, V105, P968