Analysis of bone-marrow derived fibroblasts involved in asthmatic airway remodeling and its interventional control of function
| Project/Area Number |
17590802
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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 |
Respiratory organ internal medicine
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| Research Institution | Iwate Medical University |
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Principal Investigator |
YAMAUCHI Kohei Iwate Med Univ, Scl Med, associate professor, 医学部, 助教授 (20200579)
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| Co-Investigator(Kenkyū-buntansha) |
MURAI Kazunori Iwate Med Univ, Scl Med, assistant professor, 医学部, 助手 (70285592)
OHTSU Hiroshi Tohoku Univ, Dep Technology, professor, 工学部, 教授 (60250742)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2005: ¥2,100,000 (Direct Cost: ¥2,100,000)
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| Keywords | asthma / allergic airway inflammation / remodeling / fibroblast / GFP / Bone marrow derived cells / collagen / mouse / 骨髄キメラマウス / G-CSF / コラーゲン沈着 / 線維化 / 気管支喘息 / 気道リモデリング / 粘膜線維化 / 骨髄細胞 |
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| Research Abstract |
Analysis of the asthma model with bone marrow transferred chimeric mice
Method : We made the murine asthma model with bone marrow transferred chimeric C57BL/6 mice. At two weeks after sensitization with Ovalbumin (OVA), the mice were exposed to OVA every other day during one month. Twenty four hours later from final exposure with OVA, we collected blood and broncho-alveolar lavage fluid (BAL) and obtained the lung tissue from these mice on 7^<th> day, 14^<th> day and 28^<th> day. In addition, we divided these mice into two groups. One group of the mice was administered intraperitoneally with G-CSF and the other group with saline as the control.
Estimation of histological changes was performed. The pulmonary tissue was fixed with formaldehyde and were embedded in paraffin. On the tissue sections, we estimated infiltrated inflammatory cells into airway wall as a score semi-quantitatively with Hematoxylin-Eosin staining. We identified GFP-expressing cells in bronchial tissues under chemiluminescence microscopy and also GFP positive cells with immunohistochemistry using ant-GFP antibody.
Results : On 7^<th> day after OVA exposure, eosinophils as major cells, lymphocytes and monocytes were observed in peribronchial and alveolar tissue in the chimeric mice. On 14^<th> and 28^<th> day, thickening of epithelial basement membrane and deposition of collagen in submucosal layer of bronchi became prominent. Some GFP-expressing cells were spindle-like shape under epithelium and assumed fibroblast like cells. They were also confirmed by immunohistochemistry.
GFP-expressing cells increased more in the lung of the mice with G-CSF treatment than control, and collagen deposition estimated with Elastica-Masson staining decreased in G-CSF treated mice compared to control.
Conclusion : Bone marrow derived cells were recruited to peribronchial tissue with allergic inflammation and might play a regulatory role in collagen deposition in the airway.
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Report
(3 results)
Research Products
(24 results)
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[Journal Article] Increased levels of CTGF mRNA expression in a murine model of allergic airway inflammation.2005
Author(s)
Piao H-M, Yamauchi K, Pan L-H, Nakadate T, Ito H, Mouri T, Kobayashi H, Sawai T, Nakanishi T, Takigawa M, Inoue H
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Journal Title
Allergology International 54
Pages: 105-117
NAID
Description
「研究成果報告書概要(欧文)」より
Related Report
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