Expression of membrane-bound and soluble receptor activator of NF-κB ligand (RANKL) in human T cells

被引:68
|
作者
Kanamaru, F
Iwai, H
Ikeda, T
Nakajima, A
Ishikawa, I
Azuma, M
机构
[1] Tokyo Med & Dent Univ, Grad Sch, Dept Mol Immunol, Bunkyo Ku, Tokyo 1138549, Japan
[2] Tokyo Med & Dent Univ, Grad Sch, Dept Periodontol, Tokyo 1138549, Japan
[3] Tokyo Med & Dent Univ, Grad Sch, Dept Pathol & Immunol, Tokyo 1138549, Japan
[4] Nippon Med Coll, Dept Joint Dis & Rheumatism, Tokyo 1138603, Japan
关键词
monoclonal antibody; RANKL/TRANCE; T cells; TNFR;
D O I
10.1016/j.imlet.2004.05.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The receptor activator of NF-kappaB ligand (RANKL) and its receptor RANK are critical regulators for immune responses as well as bone remodeling. RANKL is a type 11 transmembrane protein that has two forms-a membrane-anchored protein and a secreted protein. In this report, we demonstrate for the first time the kinetical expression of two forms of RANKL in human T cells using two monoclonal antibodies (mAbs) against human RANKL, which we newly derived. Freshly isolated T cells rarely expressed mRANKL, while the activation of T cells induced a substantial but minimal level of mRANKL as well as the accumulation of considerable amounts of sRANKL. The addition of the metalloprotease inhibitor KB-R8301 efficiently suppressed the release of sRANKL from activated T cells or RANKL-transfectants, and reciprocally enhanced the mRANKL expression. The membrane form of RANKL was also expressed on the infiltrating T cells in the rheumatoid synovial fluid and in the gingival tissues of patients with periodontitis. Our results demonstrate that the expression of mRANKL on T cells is strictly limited, and the majority of RANKL protein produced by T cells may be active in the soluble form after shedding. The mAbs that were derived in this study may be useful for investigating the regulation and function of RANKL in immune responses and bone remodeling. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 246
页数:8
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