Department of Biological Sciences, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea.
Eur J Immunol. 2012 Jan;42(1):58-68. doi: 10.1002/eji.201141846. Epub 2011 Dec 12.
The cytokine inducible SH2-domain protein (CISH) is a well-known STAT5 target gene, but its role in the immune system remains uncertain. In this study, we found that CISH is predominantly induced during dendritic cell (DC) development from mouse bone marrow (BM) cells and plays a crucial role in type 1 DC development and DC-mediated CTL activation. CISH knockdown reduced the expression of MHC class I, co-stimulatory molecules and pro-inflammatory cytokines in BMDCs. Meanwhile, the DC yield was markedly enhanced by CISH knockdown via cell-cycle activation and reduction of cell apoptosis. Down-regulation of cell proliferation at the later stage of DC development was found to be associated with CISH-mediated negative feedback regulation of STAT5 activation. In T-cell immunity, OT-1 T-cell proliferation was significantly reduced by CISH knockdown in DCs, whereas OT-2 T-cell proliferation was not affected by CISH knockdown. CTLs generated by DC vaccination were also markedly reduced by CISH knockdown, followed by significant impairment of DC-based tumor immunotherapy. Taken together, our data suggest that CISH expression at the later stage of DC development triggers the shutdown of DC progenitor cell proliferation and facilitates DC differentiation into a potent stimulator of CTLs.
细胞因子诱导的含 SH2 结构域蛋白(CISH)是一种众所周知的 STAT5 靶基因,但它在免疫系统中的作用仍不确定。在这项研究中,我们发现 CISH 在源自小鼠骨髓(BM)细胞的树突状细胞(DC)发育过程中主要被诱导,并且在 1 型 DC 发育和 DC 介导的 CTL 激活中发挥关键作用。CISH 敲低降低了 BMDC 中 MHC Ⅰ类、共刺激分子和促炎细胞因子的表达。同时,通过细胞周期激活和减少细胞凋亡,CISH 敲低显著增加了 DC 的产量。发现在 DC 发育的后期阶段,细胞增殖的下调与 CISH 介导的 STAT5 激活的负反馈调节有关。在 T 细胞免疫中,CISH 敲低显著降低了 OT-1 T 细胞在 DC 中的增殖,而 OT-2 T 细胞的增殖不受 CISH 敲低的影响。通过 DC 疫苗接种产生的 CTL 也显著减少,随后 DC 为基础的肿瘤免疫治疗受到显著损害。总之,我们的数据表明,CISH 在 DC 发育的后期表达触发了 DC 前体细胞增殖的关闭,并促进了 DC 分化为有效的 CTL 刺激剂。