Tissue remodeling in the acute otitis media mouse model

被引:17
作者
Sautter, Nathan B. [1 ]
Delaney, Katherine L. [2 ]
Hausman, Frances A. [2 ]
Trune, Dennis R. [2 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Otolaryngol Head & Neck Surg, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Oregon Hearing Res Ctr, Portland, OR 97201 USA
关键词
Otitis media; Mouse model; Tissue remodeling; Cytokines; BONE MORPHOGENETIC PROTEIN; CYTOKINE GENE-EXPRESSION; MATRIX METALLOPROTEINASES; EFFUSION; CHOLESTEATOMAS; MICE;
D O I
10.1016/j.ijporl.2011.07.026
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objectives: Otitis media is an infectious, inflammatory process involving the middle ear space. Chronic inflammation is associated with fibrosis, scarring and osteogenesis within the middle ear, which may contribute to subsequent hearing loss and increase the difficulty of treatment. Methods: Heat-killed Streptococcus pneumoniae was injected into the middle ears of 8-12 week old Balb/c mice. Control mice were treated with PBS middle ear injections. Middle ears were harvested at 1, 3, 5 and 7 days following injection (n = 8 for each time point). The middle ears were processed using standard RT-PCR techniques. Up- and down-regulation of mRNA expression of various members of the Bone Morphogenetic Protein (BMP), Fibroblast Growth Factor (FGF) and Matrix Metalloproteinase (MMP) families was quantified and compared to PBS treated controls (n = 8 for each time point). Results: Significant upregulation of MMP2, MMP3 and MMP9 was observed at varying time points (p < 0.05). Significant downregulation of BMP3, BMP4, BMP5 BMP6 and BMP8a was seen at varying time points (p < 0.05). Significant downregulation of FGF3, FGF6, FGF10 and FGFr1 was observed at varying time points (p < 0.05). No significant expression of BMP8b, BMP9, BMP10, FGF5, FGF8, MMP1a, MMP7 and MMP14 was detected within the middle ear. Conclusions: Inflammation within the middle ear following injection of bacterial products results in changes in the regulation of several tissue remodeling cytokines and proteinases in the mouse model. Further understanding of these molecular processes may allow for the development of treatment modalities aimed at preventing middle ear tissue remodeling. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1368 / 1371
页数:4
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