Department of Clinical Chemistry, Microbiology and Immunology, Ghent University, Ghent, Belgium.
Br J Haematol. 2013 Dec;163(5):621-30. doi: 10.1111/bjh.12588. Epub 2013 Oct 8.
Chronic lymphocytic leukaemia (CLL) is a disease with a highly variable prognosis. The clinical course can however be predicted thanks to prognostic markers. Poor prognosis is associated with expression of a B cell receptor (BCR) from unmutated immunoglobulin variable heavy-chain genes (IGHV) and expression of zeta-associated protein of 70 kDa (ZAP70). The reason why ZAP70 expression is associated with poor prognosis and whether the protein has a direct pathogenic function is at present unknown. By transfer of ZAP70 to CLL cells, we show here that expression of ZAP70 in CLL cells leads to increased expression of the nuclear factor (NF)-κB target genes interleukin-1β (IL1B), IL6 and IL8 upon BCR triggering. This could be blocked by inhibition of NF-κB signalling through inhibition of IκB kinases (IKK). Transcriptome analysis identified a NF-κB RELA signature imposed by ZAP70 expression in BCR-stimulated CLL cells. We conclude that ZAP70 acts directly as an amplifier of NF-κB signalling in CLL cells which could be an underlying mechanism for its association with poor prognosis and which may represent a therapeutic target.
慢性淋巴细胞白血病(CLL)是一种预后高度可变的疾病。然而,由于存在预后标志物,其临床过程是可以预测的。不良预后与未突变免疫球蛋白重链可变基因(IGHV)的 B 细胞受体(BCR)表达和 ζ 相关蛋白 70 kDa(ZAP70)表达相关。目前尚不清楚为什么 ZAP70 表达与不良预后相关,以及该蛋白是否具有直接的致病功能。通过将 ZAP70 转移到 CLL 细胞中,我们在这里表明,在 BCR 触发时,CLL 细胞中 ZAP70 的表达导致核因子(NF)-κB 靶基因白细胞介素 1β(IL1B)、IL6 和 IL8 的表达增加。通过抑制 IκB 激酶(IKK)抑制 NF-κB 信号转导可以阻断这种情况。转录组分析确定了 ZAP70 在 BCR 刺激的 CLL 细胞中表达所强加的 NF-κB RELA 特征。我们得出结论,ZAP70 在 CLL 细胞中直接作为 NF-κB 信号的放大器起作用,这可能是其与不良预后相关的潜在机制,并且可能代表治疗靶点。