TY - JOUR
T1 - Expression of Clara cell secretory protein in experimental otitis media in the rat
AU - Seo, Jin Kim
AU - Hak, Hyun Jung
N1 - Funding Information:
This study was supported by the Brain Korea Project 21, BMS Korea and the Institute of Communication Disorders of Korea University.
PY - 2005
Y1 - 2005
N2 - Conclusion. These results suggest that CCSP is upregulated in OME and may play a protective role in the pathogenesis of OME. Objective. Clara cell secretory protein (CCSP) is an abundant 16-kDa homodimeric protein and is secreted by non-ciliated secretory epithelial cells in the lung. It has an important protective role against the intrapulmonary inflammatory process. The aim of this study was to investigate the expression of CCSP in endotoxin-induced otitis media with effusion (OME) in the rat. Material and methods. We instilled endotoxin and saline (control) into the middle ear cavity of the rat. Middle ear mucosa were taken at 0, 1, 3, 6 and 12 h and 1, 3, 7 and 14 days, and the expression of both CCSP mRNA and protein were then evaluated using semi-quantitative reverse transcriptase polymerase chain reaction (RT-PCR), Western blotting and immunohistochemistry. Results. RT-PCR revealed that the expression of CCSP was first identified at 1 h after endotoxin instillation, was dramatically increased between 1 h and Day 1, with maximal expression at 12 h, and then decreased after Day 3. The expression pattern of CCSP protein identified by means of Western blotting was similar to the CCSP mRNA patterns observed using RT-PCR. Expression of CCSP at both mRNA and protein levels was not detected in either normal middle ear mucosa or saline-instilled middle ear mucosa. Immunohistochemistry revealed that some epithelial cells in the middle ear mucosa were stained.
AB - Conclusion. These results suggest that CCSP is upregulated in OME and may play a protective role in the pathogenesis of OME. Objective. Clara cell secretory protein (CCSP) is an abundant 16-kDa homodimeric protein and is secreted by non-ciliated secretory epithelial cells in the lung. It has an important protective role against the intrapulmonary inflammatory process. The aim of this study was to investigate the expression of CCSP in endotoxin-induced otitis media with effusion (OME) in the rat. Material and methods. We instilled endotoxin and saline (control) into the middle ear cavity of the rat. Middle ear mucosa were taken at 0, 1, 3, 6 and 12 h and 1, 3, 7 and 14 days, and the expression of both CCSP mRNA and protein were then evaluated using semi-quantitative reverse transcriptase polymerase chain reaction (RT-PCR), Western blotting and immunohistochemistry. Results. RT-PCR revealed that the expression of CCSP was first identified at 1 h after endotoxin instillation, was dramatically increased between 1 h and Day 1, with maximal expression at 12 h, and then decreased after Day 3. The expression pattern of CCSP protein identified by means of Western blotting was similar to the CCSP mRNA patterns observed using RT-PCR. Expression of CCSP at both mRNA and protein levels was not detected in either normal middle ear mucosa or saline-instilled middle ear mucosa. Immunohistochemistry revealed that some epithelial cells in the middle ear mucosa were stained.
KW - Gene expression
KW - Otitis media
KW - Polymerase chain reaction
UR - http://www.scopus.com/inward/record.url?scp=12344281692&partnerID=8YFLogxK
U2 - 10.1080/00016480410018151
DO - 10.1080/00016480410018151
M3 - Article
C2 - 15799573
AN - SCOPUS:12344281692
SN - 0001-6489
VL - 125
SP - 43
EP - 47
JO - Acta Oto-Laryngologica
JF - Acta Oto-Laryngologica
IS - 1
ER -