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Anti-inflammatory effects of Tat-Annexin protein on ovalbumin-induced airway inflammation in a mouse model of asthma

Authors
Lee, Sun HwaKim, Dae WonKim, Hye RiWoo, Su JungKim, So MiJo, Hyo SangJeon, Seong GyuCho, Sung-WooPark, Jong HoonWon, Moo HoPark, JinseuEum, Won SikChoi, Soo Young
Issue Date
Jan-2012
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Tat-Annexin-1; Asthma; MAPK; Cytokine; Protein therapy
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.417, no.3, pp 1024 - 1029
Pages
6
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
417
Number
3
Start Page
1024
End Page
1029
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/11997
DOI
10.1016/j.bbrc.2011.12.084
ISSN
0006-291X
1090-2104
Abstract
Chronic airway inflammation is a key feature of bronchial asthma. Annexin-1 (ANX1) is an anti-inflammatory protein that is an important modulator and plays a key role in inflammation. Although the precise action of ANX1 remains unclear, it has emerged as a potential drug target for inflammatory diseases such as asthma. To examine the protective effects of ANX1 protein on ovalbumin (OVA)-induced asthma in animal models, we used a cell-permeable Tat-ANX1 protein. Mice sensitized and challenged with OVA antigen had an increased amount of cytokines and eosinophils in their bronchoalveolar lavage (BAL) fluid. However, administration of Tat-ANX1 protein before OVA challenge significantly decreased the levels of cytokines (interleukin (IL)-4, IL-5, and IL-13) and BAL fluid in lung tissues. Furthermore, OVA significantly increased the activation of mitogen-activated protein kinase (MAPK) in lung tissues, whereas Tat-ANX1 protein markedly reduced phosphorylation of MAPKs such as extracellular signal-regulated protein kinase, p38, and stress-activated protein kinase/c-Jun N-terminal kinase. These results suggest that transduced Tat-ANX1 protein may be a potential protein therapeutic agent for the treatment of lung disorders including asthma. (C) 2011 Elsevier Inc. All rights reserved.
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