Interleukin-4 directly inhibits tumor necrosis factor-α-mediated osteoclast formation in mouse bone marrow macrophages

被引:31
作者
Kitaura, H
Nagata, N
Fujimura, Y
Hotokezaka, H
Tatamiya, M
Nakao, N
Yoshida, N
Nakayama, K
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Dev & Reconstruct Med, Div Microbiol & Oral Infect, Nagasaki 8528588, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Dept Dev & Reconstruct Med, Div Orthodont & Biomed Engn, Nagasaki 8528588, Japan
关键词
TNF-alpha; IL-4; osteoclast; RANKL;
D O I
10.1016/S0165-2478(03)00082-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Recently it has been found that osteoclast differentiation is induced by tumor necrosis factor (TNF)-alpha. Interleukin (IL)-4 was reported to suppress osteoclast differentiation and bone resorption. However, no study has investigated the effect of IL-4 on TNF-alpha-induced osteoclast formation. In this study, we investigated whether IL-4 inhibits TNF-alpha-mediated osteoclast formation in mouse bone marrow derived macrophages (BMM). First, IL-4 suppresses RANKL-induced osteoclast formation and bone resorption. Next, when BMM were cultured with TNF-alpha, osteoclast-like cells were formed. When they were cultured with both TNF-alpha. and IL-4, osteoclast formation and bone resorption was suppressed by IL-4 in a dose-dependent manner. It has been recently found that TNF-alpha and RANKL synergistically promote osteoclastogenesis. Finally, we investigated whether IL-4 had the ability to inhibit synergistic TNF-alpha and RANKL-induced osteoclastogenesis, with the result that it effectively inhibited the synergistic osteoclast formation in a dose-dependent manner. We conclude that IL-4 can strongly inhibit osteoclast formation that is related to both physiological bone resorption induced by RANKL and pathological bone resorption induced by TNF-alpha. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:193 / 198
页数:6
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