Kasono K, Sato K, Sato Y, Tsushima T, Shizume K, Demura H
Department of Medicine, Tokyo Women's Medical College, Japan.
Bone Miner. 1993 Jun;21(3):179-88. doi: 10.1016/s0169-6009(08)80229-2.
Recently, interleukin 4 (IL-4) was reported to inhibit bone resorption in mouse long bone culture. To test the effect of IL-4 on the formation of osteoclast-like cells, we used a mouse bone marrow culture system that formed mononuclear and multinucleated cells with osteoclast characteristics. Recombinant mouse IL-4 dose-dependently inhibited the formation of tartrate-resistant acid phosphatase-positive multinucleated cells [TRAP(+)MNC] induced by 1,25(OH)2D3, PTH(1-34) or Interleukin-1 alpha (IL-1 alpha). The minimum effective inhibitory concentration was 0.01 ng/ml, and 1 ng/ml IL-4 completely inhibited TRAP(+)MNC formation. IL-4 also dose-dependently inhibited the formation of tartrate-resistant acid phosphatase-positive mononuclear cells. Treatment of cultures with IL-4 for the first or last 48 h of an 8-day culture period inhibited TRAP(+)MNC formation to the same extent, whereas IFN-gamma and calcitonin suppressed TRAP(+)MNC formation mainly at the early and the late phase, respectively. IL-4, as a macrophage fusion factor, at higher concentrations (0.1-10 ng/ml), increased formation of tartrate-resistant acid phosphatase-negative multinucleated cells [TRAP(-)MNC] with giant macrophage characteristics. The half-maximal concentrations inhibiting TRAP(+)MNC formation and stimulating TRAP(-)MNC formation were 0.05 ng/ml and 2 ng/ml, respectively. These results demonstrate that IL-4 inhibits bone resorption by inhibiting the recruitment of osteoclast precursor and formation of multinucleated osteoclast-like cells, and by stimulating the formation of macrophage polykaryons.
最近,有报道称白细胞介素4(IL-4)可抑制小鼠长骨培养中的骨吸收。为了测试IL-4对破骨细胞样细胞形成的影响,我们使用了一种小鼠骨髓培养系统,该系统可形成具有破骨细胞特征的单核和多核细胞。重组小鼠IL-4剂量依赖性地抑制了由1,25(OH)2D3、甲状旁腺激素(1-34)或白细胞介素-1α(IL-1α)诱导的抗酒石酸酸性磷酸酶阳性多核细胞[TRAP(+)MNC]的形成。最小有效抑制浓度为0.01 ng/ml,1 ng/ml的IL-4可完全抑制TRAP(+)MNC的形成。IL-4也剂量依赖性地抑制抗酒石酸酸性磷酸酶阳性单核细胞的形成。在8天培养期的第1个或最后48小时用IL-4处理培养物,对TRAP(+)MNC形成的抑制程度相同,而干扰素-γ和降钙素分别主要在早期和晚期抑制TRAP(+)MNC的形成。IL-4作为一种巨噬细胞融合因子,在较高浓度(0.1-10 ng/ml)下,可增加具有巨大巨噬细胞特征的抗酒石酸酸性磷酸酶阴性多核细胞[TRAP(-)MNC]的形成。抑制TRAP(+)MNC形成和刺激TRAP(-)MNC形成的半数最大浓度分别为0.05 ng/ml和2 ng/ml。这些结果表明,IL-4通过抑制破骨细胞前体的募集和多核破骨细胞样细胞的形成,以及刺激巨噬细胞多核体的形成来抑制骨吸收。