Yang Lu-Lu, Sun Zi-Min, Liu Xin, Zhu Xiao-Yu, Wang Xing-Bing, Wang Jian
Department of Hematology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei 23001, Auhui Province, China.
Department of Hematology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei 23001, Auhui Province, China. E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014 Oct;22(5):1415-21. doi: 10.7534/j.issn.1009-2137.2014.05.044.
This study was aimed to investigate the effect of high mobility group box1(HMGB1) and/or stromal cell derived factor-1(SDF-1) on the migration of cord blood CD34⁺ cells, and to explore whether HMGB1 promotes cord blood CD34⁺ cell migration via SDF-1/CXCR4 axis. Cord blood mononuclear cells were isolated by Ficoll-Paque density centrifugation, CD34⁺ cells were collected by a positive immunoselection procedure (CD34 MicroBeads) according to the manufacturer's instructions, the purity of the isolated CD34⁺ cells was detected by flow cytometry. In vitro chemotaxis assays were performed using Transwell cell chambers to detect cells migration. 1 × 10⁵ cells/well cord blood CD34⁺ cells were added into the upper chambers. Different concentrations of HMGB1 and/or SDF-1 (0, 10, 25, 50, 100, 200 ng/ml) were used to detect the optimal concentrations of HMGB1 and/or SDF-1 for inducing migration of cord blood CD34⁺ cells. Freshly isolated cord blood CD34⁺ cells express CXCR4 (SDF-1 receptor), and HMGB1 receptor TLR-2,TLR-4 and RAGE. To explore which receptors were required for the synergy of HGMB1 and/or SDF-1 on cells migration, the anti-SDF-1, anti-CXCR4 and anti-RAGE antibodies were used to detect the effect of HGMB1 alone or with SDF-1 on cord blood CD34⁺ cells migration. The results showed that the purity of CD34⁺ cells isolated from cord blood mononuclear cells by magnetic cell sorting was 97.40 ± 1.26%, the 25 ng/ml SDF-1 did not induce migration of cord blood CD34⁺ cells, whereas the optimal migration was observed at 100 ng/ml. HMGB1 alone did not induce migration up to 100 ng/ml. The dose test found that the the best synergistic concentrations for cells migration were 100 ng/ml HMGB1 combined with 50 ng/ml SDF-1. The blocking test showed that both the anti-SDF-1 (4 µg/ml) and anti-CXCR4 (5 µg/ml) antibodies could block cell migration induced by HMGB1 or combined with SDF-1, but the cord blood CD34⁺ cells in the presence of anti-RAGE, anti-TLR-2 and anti-TLR-4 antibodies did not modify the response to SDF-1 in the presence of HMGB1. It is concluded that both HMGB1 and SDF-1 can induce cord blood CD34⁺ cells migration, HMGB1 enhances SDF-1-induced migration exclusively via CXCR4 and in a RAGE and TLR receptors-independent manner, the exact mechanism needs to be further explored.
本研究旨在探讨高迁移率族蛋白B1(HMGB1)和/或基质细胞衍生因子-1(SDF-1)对脐血CD34⁺细胞迁移的影响,并探讨HMGB1是否通过SDF-1/CXCR4轴促进脐血CD34⁺细胞迁移。采用Ficoll-Paque密度梯度离心法分离脐血单个核细胞,按照制造商的说明通过阳性免疫筛选程序(CD34微珠)收集CD34⁺细胞,采用流式细胞术检测分离的CD34⁺细胞的纯度。使用Transwell细胞小室进行体外趋化试验以检测细胞迁移。将1×10⁵个细胞/孔的脐血CD34⁺细胞加入上室。使用不同浓度的HMGB1和/或SDF-1(0、10、25、50、100、200 ng/ml)来检测诱导脐血CD34⁺细胞迁移的HMGB1和/或SDF-1的最佳浓度。新鲜分离的脐血CD34⁺细胞表达CXCR4(SDF-1受体)以及HMGB1受体TLR-2、TLR-4和RAGE。为了探究HGMB1和/或SDF-1协同作用于细胞迁移需要哪些受体,使用抗SDF-1、抗CXCR4和抗RAGE抗体来检测单独的HGMB1或与SDF-1联合使用时对脐血CD34⁺细胞迁移的影响。结果显示,通过磁性细胞分选从脐血单个核细胞中分离出的CD34⁺细胞的纯度为97.40±1.26%,25 ng/ml的SDF-1未诱导脐血CD34⁺细胞迁移,而在100 ng/ml时观察到最佳迁移效果。单独的HMGB1在高达100 ng/ml时未诱导迁移。剂量试验发现细胞迁移的最佳协同浓度为100 ng/ml的HMGB1与50 ng/ml的SDF-1联合使用。阻断试验表明,抗SDF-1(4 µg/ml)和抗CXCR4(5 µg/ml)抗体均可阻断由HMGB1或与SDF-1联合诱导的细胞迁移,但在存在抗RAGE、抗TLR-2和抗TLR-4抗体的情况下,脐血CD34⁺细胞对存在HMGB1时SDF-1的反应未发生改变。结论是,HMGB1和SDF-1均可诱导脐血CD34⁺细胞迁移,HMGB1仅通过CXCR4以RAGE和TLR受体非依赖性方式增强SDF-1诱导的迁移,确切机制有待进一步探索。