Department of Paediatrics, The Chinese University of Hong Kong, Shatin, Hong Kong.
Blood. 2011 Feb 10;117(6):1840-50. doi: 10.1182/blood-2010-04-281329. Epub 2010 Nov 9.
The stromal cell-derived factor-1 (SDF-1)/chemokine C-X-C receptor 4 (CXCR4) axis plays a critical role in homing and engraftment of hematopoietic stem/progenitor cells (HSCs) during bone marrow transplantation. To investigate the transcriptional regulation provided by this axis, we performed the first differential transcriptome profiling of human cord blood CD34(+) cells in response to short-term exposure to SDF-1 and identified a panel of genes with putative homing functions. We demonstrated that CD9, a member of the tetraspanin family of proteins, was expressed in CD34(+)CD38(-/lo) and CD34(+)CD38(+) cells. CD9 levels were enhanced by SDF-1, which simultaneously down-regulated CXCR4 membrane expression. Using specific inhibitors and activators, we demonstrated that CD9 expression was modulated via CXCR4, G-protein, protein kinase C, phospholipase C, extracellular signal-regulated kinase, and Janus kinase 2 signals. Pretreatment of CD34(+) cells with the anti-CD9 monoclonal antibody ALB6 significantly inhibited SDF-1-mediated transendothelial migration and calcium mobilization, whereas adhesion to fibronectin and endothelial cells was enhanced. Pretreatment of CD34(+) cells with ALB6 significantly impaired their homing to bone marrow and spleen of sublethally irradiated NOD/SCID (nonobese diabetic/severe combined immune-deficient) mice. Sorted CD34(+)CD9(-) cells displayed lower bone marrow homing capacity compared with that of total CD34(+) cells. CD9 expression on homed CD34(+) cells was significantly up-regulated in vivo. Our results indicate that CD9 might possess specific functions in HSC homing.
基质细胞衍生因子-1(SDF-1)/趋化因子 C-X-C 受体 4(CXCR4)轴在骨髓移植过程中造血干细胞/祖细胞(HSCs)的归巢和植入中起着关键作用。为了研究该轴提供的转录调控,我们首次对人脐血 CD34(+)细胞对 SDF-1 短期暴露的反应进行了差异转录组谱分析,并确定了一组具有潜在归巢功能的基因。我们证明,CD9 是四跨膜蛋白家族的成员之一,在 CD34(+)CD38(-/lo)和 CD34(+)CD38(+)细胞中表达。SDF-1 增强了 CD9 的表达,同时下调了 CXCR4 膜表达。使用特异性抑制剂和激活剂,我们证明 CD9 的表达通过 CXCR4、G 蛋白、蛋白激酶 C、磷脂酶 C、细胞外信号调节激酶和 Janus 激酶 2 信号进行调节。用抗 CD9 单克隆抗体 ALB6 预处理 CD34(+)细胞可显著抑制 SDF-1 介导的跨内皮迁移和钙动员,而黏附到纤维连接蛋白和内皮细胞的能力增强。用 ALB6 预处理 CD34(+)细胞可显著损害其向亚致死照射的 NOD/SCID(非肥胖型糖尿病/严重联合免疫缺陷)小鼠骨髓和脾脏的归巢。与总 CD34(+)细胞相比,分选的 CD34(+)CD9(-)细胞的骨髓归巢能力较低。体内归巢的 CD34(+)细胞上的 CD9 表达明显上调。我们的结果表明,CD9 可能在 HSC 归巢中具有特定的功能。