Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Miao, H. | Xue, Q.F. | Hu, Q.H. | Zhang, H. | Wang, L.R. | Niimi, H. | Zhuang, F.Y.
Affiliations: Department of Biorheology, China–Japan Friendship Institute of Clinical Medical Sciences, Beijing 100029, China | Department of Pathophysiology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing 100005, China | National Cardiovascular Center Research Institute, Suita, Osaka 565, Japan
Abstract: In situ expression of ICAM‐1 and ICAM‐1 mRNA on the lung tissue of asthmatic rats was studied by immunohistochemical staining and in situ hybridization, respectively. The results showed that in normal rats ICAM‐1 expression was rare on the endothelium of pulmonary artery and vein, and on the bronchial and alveolar epithelium. The distribution of ICAM‐1 expression on the different part of lung tissue of asthmatic rats was similar to that of normal rats, but the level of ICAM‐1 expression was significantly increased on the endothelium of pulmonary artery (EPA) and vein (EPV), bronchial epithelium (BEP) and alveolar epithelium (AEP) compared with those of normal and sensitized controls. The distribution and expression of ICAM‐1 mRNA on the different part of lung tissue of normal and asthmatic rats were similar to that of ICAM‐1 expression. In asthmatic rats, the expression of ICAM‐1 mRNA on AEP and EPV was increased significantly compared with those of normal and sensitized controls. It is concluded that the increase of ICAM‐1 expression on endothelium of pulmonary vessels, epithelium of broncheoli and alveoli may play an important role of inflammatory cell infiltration in asthmatic rats, and the increased expression of ICAM‐1 in asthmatic rats was caused by the increase of expression of ICAM‐1 mRNA.
Keywords: ICAM‐1, ICAM‐1 mRNA, asthma, rat
Journal: Clinical Hemorheology and Microcirculation, vol. 17, no. 4, pp. 325-331, 1997
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]