| Literature DB >> 16168397 |
Naomi Yamashita1, Hiroyuki Tashimo, Hirofuni Ishida, Yukiko Matsuo, Hidenori Arai, Hiroyuki Nagase, Tetsuya Adachi, Ken Ohta.
Abstract
Insulin-like growth factor (IGF)-I is known to act on fibroblasts as a progression factor to push cells toward proliferation and activation to synthesize collagen. Subepithelial fibrosis, collagen deposition at the lamina reticularis, is part of the process of so-called remodeling and is a characteristic finding in the asthmatic airway. To study the role of IGF in the evolution of asthma, we used a model that involved immunization of mice with ovalbumin and alum, followed by an inhaled challenge of ovalbumin. IGF-I neutralizing antibody was continuously infused with an osmotic pump. Pulmonary function was analyzed using whole-body plethysmography before and after acetylcholine administration. It was found that OVA inhalation induced IGF-I expression at the site of the airway. IGF-I neutralizing Ab inhibited the elevation of airway resistance, airway inflammation, and an increase in airway wall thickening. The depression of ICAM-1 expression was accompanied by a diminution in airway inflammation. In conclusion, these results suggest that IGF-I is likely to be an important mediator of inflammation and remodeling in the asthmatic airway.Entities:
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Year: 2005 PMID: 16168397 DOI: 10.1016/j.cellimm.2005.07.006
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868