Intracellular signal transduction mechanisms of airway epithelial cells in allergic conditions
| Project/Area Number |
16591705
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Otorhinolaryngology
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| Research Institution | Mie University |
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Principal Investigator |
TAKEUCHI Kazuhiko Mie University, School of Medicine, Associate professor, 大学院・医学系研究科, 助教授 (50206942)
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| Co-Investigator(Kenkyū-buntansha) |
YUTA Atsushi Mie University, Department of University Hospital, Assistant professor, 医学部附属病院, 講師 (80293778)
岸岡 睦子 三重大学, 医学部, 助手 (10314113)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 2005: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2004: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | NF-κB / thrombin / mucin / leukotrienes / signal transduction / PAR / cellular structural proteins / permeability / G-protein / PKC / MEK |
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| Research Abstract |
Recently, it is believed that epithelial cells play important roles in allergic conditions as in allergic rhinitis. We tried to elucidate the intracellular signal transduction mechanisms by which mediators have effects on functional changes in epithelial cells.
1.Mechanism by which leukotrienes activate mucin gene transcription
Leukotriene D_4 (LTD_4) has been shown to induce mucus secretion in the airway. However, nothing has previously been known about the effect of LTD_4 on mucin gene expression. Reporter gene assay was mainly used for analysis. We found that NF-κB is required for LTD_4-induced MUC2 gene transcription in a CysLT_1R-dependent manner. Taken together, our findings suggest that LTD_4 up-regulates MUC2 gene transcription via a signaling pathway involving CysLT_1R, G-protein, PKC, MEK, ERK and NF-κB.
2.Mechanism by which thrombin increases permeability in epithelial cells
Recently, thrombin was reported to be increased in the airway of patients with asthma, and thrombin has b
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een shown to increase the permeability of endothelial cell monolayers. Therefore, we suspected that thrombin affects airway permeability. Calu-3 cell monolayers were established on microporous membranes of tissue culture cell inserts. We examined the effects of topically applied thrombin or thrombin receptor activating peptide (TRAP) on : (1) transepithelial permeability (luminal to serosal transfer) of radiolabeled mannitol and albumin, (2) changes in electrical resistance, and (3) actin fiber content as assessed by fluorescence microscopy. Compared with untreated control cultures, treatment of the monolayers for 24 h with thrombin or TRAP significantly decreased the electrical resistance and increased the permeability to mannitol and albumin. In addition, these treatments enhanced the appearance of actin stress fibers, and small gaps became visible at areas of cell-cell contact. Thrombin appears to increase epithelial permeability by receptor-mediated reorganization of the actin network in airway epithelial cells. This is likely to contribute to the impairment of the airway barrier function. Less
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Report
(3 results)
Research Products
(12 results)
