白细胞介素-10驱动人单核细胞转化为CD16阳性巨噬细胞。

Journal of inflammation Pub Date : 1996-01-01
J C Calzada-Wack, M Frankenberger, H W Ziegler-Heitbrock
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引用次数: 0

摘要

单核细胞/巨噬细胞谱系的细胞是异质的,一些类型表达CD16分子(IgG的Fc受体,III型),而另一些则是阴性的。我们现在表明,用白细胞介素-10 (IL-10)培养人血液单核细胞将在18小时内诱导高水平的细胞表面CD16,并且这与转录物水平的增加有关。在长时间培养36小时后,对照培养物也成为CD16阳性,抗il -10可以阻止这种诱导,但抗肿瘤坏死因子(TNF)抗体或同型对照不能阻止这种诱导。体外培养血单核细胞导致骨髓单核细胞干细胞抗原CD33的自发降低,表明细胞成熟。IL-10处理将加速这一过程,并导致细胞表面CD33的进一步减少。这些数据表明,IL-10促进单核细胞成熟,并指导这些细胞发育成CD16阳性巨噬细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interleukin-10 drives human monocytes to CD16 positive macrophages.

Cells of the monocyte/macrophage lineage are heterogenous in that some types express the CD16 molecule (Fc receptor for IgG, type III), while others are negative. We now show that culture of human blood monocytes with interleukin-10 (IL-10) will induce high levels of cell surface CD16 within 18 hr, and this goes along with increased transcript levels. After prolonged culture for 36 hr, control cultures also become CD16 positive and this induction can be prevented by anti-IL-10, but not by anti-tumor necrosis factor (TNF) antibody or isotype control. In vitro culture of blood monocytes results in a spontaneous decrease of the myelomonocytic stem cell antigen CD33, suggesting that the cells undergo maturation. IL-10 treatment will accelerate this process and result in a further reduction of cell surface CD33. These data indicate that IL-10 promotes monocyte maturation and directs these cells to develop into CD16 positive macrophages.

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