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Desthiobiotin-Streptavidin-Affinity Mediated Purification of RNA-Interacting Proteins in Mesothelioma Cells
Published on: April 25, 2018
Double-stranded RNA poly(I:C) enhances matrix metalloproteinase mRNA expression in human nasal polyp epithelial cells
Jiyun Wang1, So Watanabe, Satoshi Matsukura
1Department of Otorhinolaryngology, Showa University School of Medicine, Tokyo, Japan.
Conclusion:
The significant up-regulation of matrix metalloproteinase (MMP)-9 mRNA, which is not modulated by tissue inhibitor of metalloproteinase (TIMP)-1, is an additional source of increased proteolytic activity in virus-infected upper airways that might contribute to the exacerbation of chronic rhinosinusitis with nasal polyps.
Objectives:
Chronic rhinosinusitis is often exacerbated by viral infection. We hypothesized that a disruption of the mechanisms that regulate the activity of MMPs during viral infection is one possible mechanism responsible for the exacerbation. In the present study we attempted to achieve a better understanding of MMP expression in nasal epithelial cells after viral infection.
Materials And Methods:
Human nasal epithelial cells were isolated from nasal polyp specimens obtained during endoscopic endonasal surgery in chronic rhinosinusitis patients. We investigated the expression of MMP-2, MMP-9, and TIMP-1 mRNA in primary human nasal polyp epithelial cells after dsRNA stimulation.
Results:
Among the genes whose expression was evaluated, only expression of MMP-9 mRNA increased significantly after dsRNA stimulation.
Insights
Viral infection significantly increases matrix metalloproteinase (MMP)-9 mRNA in upper airways. This heightened proteolytic activity may worsen chronic rhinosinusitis with nasal polyps.
Area of Science:
- Otolaryngology
- Immunology
- Molecular Biology
Background:
- Chronic rhinosinusitis (CRS) is frequently exacerbated by viral infections.
- Viral infections may disrupt the regulation of matrix metalloproteinases (MMPs), contributing to CRS exacerbation.
- Understanding MMP expression in nasal epithelium during viral infection is crucial.
Purpose of the Study:
- To investigate the expression of MMP-2, MMP-9, and TIMP-1 mRNA in nasal polyp epithelial cells following viral stimulation.
- To elucidate the role of MMP dysregulation in viral-induced exacerbation of chronic rhinosinusitis.
Main Methods:
- Primary human nasal polyp epithelial cells were isolated from CRS patients.
- Cells were stimulated with dsRNA to mimic viral infection.
- Expression levels of MMP-2, MMP-9, and TIMP-1 mRNA were quantified.
Main Results:
- Only MMP-9 mRNA expression was significantly upregulated after dsRNA stimulation.
- TIMP-1 expression did not show significant modulation in response to dsRNA.
Conclusions:
- Significant upregulation of MMP-9 mRNA occurs in virus-infected upper airway epithelial cells.
- This increased MMP-9 contributes to elevated proteolytic activity.
- This may exacerbate chronic rhinosinusitis with nasal polyps.
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