兰克尔
细胞分化
分子生物学
CD8型
细胞毒性T细胞
细胞生物学
单核细胞
抗原提呈细胞
CD40
免疫学
生物
T细胞
医学
抗原
免疫系统
体外
内科学
受体
生物化学
激活剂(遗传学)
基因
作者
Masahiro Kondo,Yohko Murakawa,Takafumi Matsumura,Mako Moriyama,Yoshimasa Sumita,Nanae Harashima,Mamoru Harada
标识
DOI:10.1136/annrheumdis-2014-eular.1416
摘要
Background
Activated T cells express RANKL and have been considered to pomote osteoclast (OC) differentiation. Alternatively, activated T cells were suggested to suppress OC differentiation via the production of IL-4 and IL-10. Additionally, in a mouse model, activated T cells were reported to drive monocytes to differentiate into dendritic cells (DCs) through GM-CSF production. 1) Objectives
In this study, we investigated effects of CD4+ T cells or CD8+ T cells with or without IL-2 on the induction of OC from human monocytes. Methods
Monocytes, CD4+ T cells, and CD8+ T cells were prepared from PBMC of healthy volunteers. After incubation of monocytes with RANKL (50 ng/ml) and M-CSF (20 ng/ml) for 14 days, OC differentiation was evaluated by the TRAP staining. Additionally, we added CD4+T cells or CD8+T cells with or without IL-2 (20U/ml) at the initiation of the culture. Results
Apparent OCs were induced from human monocytes by the culture with RANKL and M-CSF. The addition of CD8+ T cells facilitated the OC differentiation. Conversely, the addition of CD4+ T cells with IL-2 remarkably inhibited the OC differentiation, with preferential induction of DCs. Conclusions
CD8+ T cells seem to facilitate OC differentiation from monocytes. Alternatively, irrespective of the presence of RANKL and M-CSF, CD4+ T cells with IL-2 facilitate DC differentiation, thereby resulting in drastic inhibition of OC differentiation. References
Miyamoto T, Ohneda O, Arai F, Iwamoto K, Okada S, Takagi K, et al. Bifurcation of osteoclasts and dendritic cells from common progenitors. Blood. 2001,15;98(8):2544-54. Disclosure of Interest
None declared DOI
10.1136/annrheumdis-2014-eular.1416
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