Pattern changes of mucin gene expression with pneumococcal otitis media

被引:20
作者
Tsuboi, Y
Kim, Y
Paparella, MM
Chen, NQ
Schachern, PA
Lin, JZ
机构
[1] Univ Minnesota, Sch Med, Dept Otolaryngol, Otitis Media Res Ctr, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Pediat, Minneapolis, MN 55455 USA
[3] Minnesota Ear Head & Neck Clin, Minneapolis, MN 55454 USA
关键词
otitis media; mucin genes; S; pneumoniae; middle ear; rats;
D O I
10.1016/S0165-5876(01)00540-7
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: mucins, known to be important components of the mucociliary transport system in the middle ear and Eustachian tube, are subject to changes under inflammatory conditions. Which mucin genes are up-regulated or activated during an inflammatory reaction of the middle ear and Eustachian tube, however, is poorly understood. The purpose of this study was to characterize mucin gene expression in middle ears and Eustachian tubes with pneumococcal ear infection. Methods: sixteen rats received intrabullar inoculation of Streptococcus pneumoniae type 6A at 2,5 x 10(6) colony forming units (CFU). Four animals were sacrificed on days 1, 3, 7, and 14, respectively. The profile of mucin gene expression in the middle car and Eustachian tube was examined by reverse transcription polymerase chain reaction (RT-PCR) at the above time points. Sixteen rats that received intrabullar inoculation of phosphate-buffered saline (PBS) served as controls. Results: the Muc2 mucin gene was expressed in middle ear mucosa of the control rats. Following pneumococcal inoculation, Muc1-Muc-5 mucin genes were expressed in the middle ear mucosa in a time-dependent manner. In the Eustachian tube. the Muc2, Muc4 and Muc5 mucin genes were expressed in both control and pneumococcal inoculation groups. Conclusion: Muc1, Muc3, Muc4, and Muc5 mucin genes were activated in the middle ear mucosa by pneumococci, which may contribute to hyper-production of mucin in acute pneumococcal otitis media. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
相关论文
共 40 条
[1]   IDENTIFICATION OF AN ACTIVE DISACCHARIDE UNIT OF A GLYCOCONJUGATE RECEPTOR FOR PNEUMOCOCCI ATTACHING TO HUMAN PHARYNGEAL EPITHELIAL-CELLS [J].
ANDERSSON, B ;
DAHMEN, J ;
FREJD, T ;
LEFFLER, H ;
MAGNUSSON, G ;
NOORI, G ;
EDEN, CS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 158 (02) :559-570
[2]   EVIDENCE FOR DIFFERENT HUMAN TRACHEOBRONCHIAL MUCIN PEPTIDES DEDUCED FROM NUCLEOTIDE CDNA SEQUENCES [J].
AUBERT, JP ;
PORCHET, N ;
CREPIN, M ;
DUTERQUECOQUILLAUD, M ;
VERGNES, G ;
MAZZUCA, M ;
DEBUIRE, B ;
PETITPREZ, D ;
DEGAND, P .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 5 (02) :178-185
[3]   FROM THE CENTER-FOR-DISEASE-CONTROL - EPIDEMIOLOGY OF PNEUMOCOCCAL SEROTYPES IN THE UNITED-STATES, 1978-1979 [J].
BROOME, CV ;
FACKLAM, RR ;
ALLEN, JR ;
FRASER, DW ;
AUSTRIAN, R .
JOURNAL OF INFECTIOUS DISEASES, 1980, 141 (01) :119-123
[4]  
BROWN DT, 1985, ARCH OTOLARYNGOL, V111, P688
[5]   PSEUDOMONAS-AERUGINOSA OUTER-MEMBRANE ADHESINS FOR HUMAN RESPIRATORY MUCUS GLYCOPROTEINS [J].
CARNOY, C ;
SCHARFMAN, A ;
VANBRUSSEL, E ;
LAMBLIN, G ;
RAMPHAL, R ;
ROUSSEL, P .
INFECTION AND IMMUNITY, 1994, 62 (05) :1896-1900
[6]   An intramembrane modulator of the ErbB2 receptor tyrosine kinase that potentiates neuregulin signaling [J].
Carraway, KL ;
Rossi, EA ;
Komatsu, M ;
Price-Schiavi, SA ;
Huang, DM ;
Guy, PM ;
Carvajal, ME ;
Fregien, N ;
Carraway, CAC ;
Carraway, KL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) :5263-5266
[7]   Multiple facets of sialomucin complex/MUC4, a membrane mucin and ErbB2 ligand, in tumors and tissues (Y2K update) [J].
Carraway, KL ;
Price-Schiavi, SA ;
Komatsu, M ;
Idris, N ;
Perez, A ;
Li, P ;
Jepson, S ;
Zhu, XY ;
Carvajal, ME ;
Carraway, CAC .
FRONTIERS IN BIOSCIENCE, 2000, 5 :D95-D107
[8]   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
[9]  
CARROLL SM, 1981, J BIOL CHEM, V256, P8357
[10]  
CHONCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156