RETRACTED: Activation of discoidin domain receptor 1 on CD14-positive pronchoalveolar lavage fluid cells induces chemokine production in idiopathic pulmonary fibrosis (Retracted Article. See vol 181, pg 6672, 2008)

被引:34
作者
Matsuyama, W
Watanabe, M
Shirahama, Y
Oonakahara, KI
Higashimoto, I
Yoshimura, T
Osame, M
Arimura, K
机构
[1] Kagoshima Univ Hosp, Resp & Stress Care Ctr, Div Resp Med, Kagoshima 8908520, Japan
[2] NCI, Frederick Canc Res & Dev Ctr, Mol Immunoregulat Lab, Canc Res Ctr, Frederick, MD 21702 USA
关键词
D O I
10.4049/jimmunol.174.10.6490
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Discoidin domain receptor. 1 (DDR1) is a receptor tyrosine kinase activated by collagen. We previously reported the functional expression of DDR1 on human monocyte-derived macrophages in vitro; however, information regarding its role in diseases is limited. Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease, and the lesions contain an abundance of collagen. In this study, we examined DDR1 expression on bronchoalveolar lavage fluid (BALF) cells and investigated its functionality using samples obtained from 28 IPF patients, 13 chronic obstructive pulmonary disease patients, and 14 healthy volunteers. The DDR1 expression level in CD14-positive BALF cells was higher in IPF patients than in chronic obstructive pulmonary disease patients or healthy volunteers. The predominant isoform was DDR1b in the IPF group, while DDR1a was predominant in the other two groups. Using immunohistochemical analysis, we also detected DDR1 expression on infiltrating inflammatory cells in the IPF lesion. In IPF patients, DDR1 activation induced the production of MCP-1, IL-8, MIP-1 alpha, and matrix metalloproteinase-9 (MMP-9) from CD14-positive BALF cells in a p38 MAPK-dependent manner. In contrast, DDRI activation of CD14-positive BALF cells in the other groups did not induce the production of these chemokines or MMP-9. These chemokines and MMP-9 contribute to the development of IPF and, therefore, we suggest that DDRI might be associated with the pathogenesis of IPF in the tissue microenvironment.
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页码:6490 / 6498
页数:9
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