Z39Ig is expressed on macrophages and may mediate inflammatory reactions in arthritis and atherosclerosis

被引:36
作者
Lee, Min-Young
Kim, Won-Jung
Kang, Yoon-Joong
Jung, Young-Mi
Kang, Young-Mo
Suk, Kyoungho
Park, Jeong-Euy
Choi, Eun-Mi
Choi, Beom-Kyu
Kwon, Byoung S.
Lee, Won-Ha [1 ]
机构
[1] Kyungpook Natl Univ, Dept Genet Engn, Coll Nat Sci, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Sch Med, Agrobiotechnol Educ Ctr, Taegu 702701, South Korea
[3] Kyungpook Natl Univ, Sch Med, Dept Rheumatol, Taegu 702701, South Korea
[4] Kyungpook Natl Univ, Sch Med, Dept Pharmacol, Taegu 702701, South Korea
[5] Sungkyunkwan Univ, Samsung Med Ctr, Div Cardiol, Seoul, South Korea
[6] Univ Ulsan, Immunomodulat Res Ctr, Ulsan 680749, South Korea
关键词
matrix metalloproteinase; extracellular matrix; rheumatoid arthritis;
D O I
10.1189/jlb.0306160
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Z39Ig is a transmembrane protein containing two Ig homology domains with unknown functions. Immunohistochemical analyses of human carotid atherosclerotic plaques detected Z39Ig staining in areas rich in foamy macrophages. Z39Ig staining was also observed in macrophages in the lining layers and sublining areas of rheumatoid arthritis synovium. Z39Ig staining in the osteoarthritis synovium was restricted to macrophages in the lining layers. To identify the role(s) of Z39Ig in the function of macrophages, we used human monocytic cell lines TF-1A (Z39Ig-negative) and THP-1 (Z39Ig-positive). The expression of Z39Ig was induced in TF-1A cells,when they were differentiated into macrophages by treatment with PMA. The stimulation of PMA-treated TF-1A or THP-1 cells with immobilized anti-Z39Ig mAb induced the secretion of IL-8 and matrix metalloproteinase (MMP)-9, which was dependent on NF-kappa B activation. These data indicate that the macrophage Z39Ig is involved in the pathogenesis of inflammatory diseases through chemokine induction, which will promote the migration of inflammatory cells into the lesion area, and MMP-9 induction, which will contribute to cartilage destruction or extracellular matrix degradation.
引用
收藏
页码:922 / 928
页数:7
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