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DOI 10.1080/00016489.2016.1179786

Медицинская библиотека · Acta oto-laryngologica · 2016

Expression of macrophage migration inhibitory factor and CD74 in the inner ear and middle ear in lipopolysaccharide-induced otitis media.

Ishihara Hisashi, Kariya Shin, Okano Mitsuhiro, Zhao Pengfei, Maeda Yukihide, Nishizaki Kazunori

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Аннотация

CONCLUSION

Significant expression of macrophage migration inhibitory factor and its receptor (CD74) was observed in both the middle ear and inner ear in experimental otitis media in mice. Modulation of macrophage migration inhibitory factor and its signaling pathway might be useful in the management of inner ear inflammation due to otitis media.

OBJECTIVES

Inner ear dysfunction secondary to otitis media has been reported. However, the specific mechanisms involved are not clearly understood. The aim of this study is to investigate the expression of macrophage migration inhibitory factor and CD74 in the middle ear and inner ear in lipopolysaccharide-induced otitis media.

METHOD: BALB/c mice received a transtympanic injection of either lipopolysaccharide or phosphate-buffered saline (PBS). The mice were sacrificed 24 h after injection, and temporal bones were processed for polymerase chain reaction (PCR) analysis, histologic examination, and immunohistochemistry.

RESULTS

PCR examination revealed that the lipopolysaccharide-injected mice showed a significant up-regulation of macrophage migration inhibitory factor in both the middle ear and inner ear as compared with the PBS-injected control mice. The immunohistochemical study showed positive reactions for macrophage migration inhibitory factor and CD74 in infiltrating inflammatory cells, middle ear mucosa, and inner ear in the lipopolysaccharide-injected mice.

Для цитирования: Ishihara Hisashi, Kariya Shin, Okano Mitsuhiro, Zhao Pengfei, Maeda Yukihide, Nishizaki Kazunori. Expression of macrophage migration inhibitory factor and CD74 in the inner ear and middle ear in lipopolysaccharide-induced otitis media.. Acta oto-laryngologica. 2016. DOI: 10.1080/00016489.2016.1179786.

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