Jin Feng-Yan, Qiu Lu-Gui, Li Qiao-Chuan, Meng Heng-Xing, Wang Ya-Fei, Yu Zhen, Li Qian, Han Jun-Lin
State Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Zhonghua Xue Ye Xue Za Zhi. 2007 Feb;28(2):98-102.
To explore the role of stromal cell-derived factor (SDF-1) and its specific receptor CXCR4 in the G-CSF-induced hematopoietic stem/progenitor cells (HSPCs) mobilization in human healthy donor.
The changes of SDF-1/CXCR4 in bone marrow (BM) and peripheral blood (PB) of healthy donors during G-CSF-induced mobilization were detected by enzyme-linked immunosorbent assay (ELISA), immunohistological staining and flow cytometry. SDF-1 neutralizing antibody wes injected into BALB/c mice to further test its effect on mobilization.
SDF-1 concentration in mobilized BM (mBM), steady state BM (ssBM) and PB were(7.23 +/- 0.66) microg/L, (5.43 +/- 0.35) microg/L and (5.42 +/- 0.52) microg/L, respectively. SDF-1 protein levels were decreased in the BM (P < 0.05) after 5-day G-CSF injection, and its concentration gradient between BM and PB disappeared (P > 0.05). Significant up-regulation of CXCR4 expression was observed on mBM CD34 cells in healthy donors. The rate of CXCR4 expression on CD34 cells in ssBM, mBM and mobilized PB were (40.98 +/- 21.56)%, (65.80 +/- 24.68)% and (27.54 +/- 26.03)%, respectively. Comparing with that in ssBM and mBM, CXCR4 expression on mobilized PB CD34+ cells were significantly decreased (P < 0.05). Inhibition of SDF-1 signal by blocking monoclonal antibodies significantly reduced G-CSF-induced mobilization in BALB/c mice. This resulted in significant decrease of white blood cell count and progenitors mobilized into peripheral circulation.
G-CSF induces HSPCs mobilization by decreasing bone marrow SDF-1 and down-regulating CXCR4 expression on HSPCs.
探讨基质细胞衍生因子(SDF-1)及其特异性受体CXCR4在粒细胞集落刺激因子(G-CSF)诱导健康供者造血干/祖细胞(HSPCs)动员中的作用。
采用酶联免疫吸附测定(ELISA)、免疫组织化学染色及流式细胞术检测健康供者在G-CSF诱导动员过程中骨髓(BM)和外周血(PB)中SDF-1/CXCR4的变化。将SDF-1中和抗体注射到BALB/c小鼠体内,进一步检测其对动员的影响。
动员骨髓(mBM)、稳态骨髓(ssBM)和外周血中SDF-1浓度分别为(7.23±0.66)μg/L、(5.43±0.35)μg/L和(5.42±0.52)μg/L。注射G-CSF 5天后,骨髓中SDF-1蛋白水平降低(P<0.05),骨髓与外周血之间的浓度梯度消失(P>0.05)。健康供者mBM CD34细胞上CXCR4表达显著上调。ssBM、mBM和动员外周血中CD34细胞上CXCR4表达率分别为(40.98±21.56)%、(65.80±24.68)%和(27.54±26.03)%。与ssBM和mBM相比,动员外周血CD34+细胞上CXCR4表达显著降低(P<0.05)。通过阻断单克隆抗体抑制SDF-1信号可显著降低BALB/c小鼠中G-CSF诱导的动员。这导致白细胞计数显著降低,进入外周循环的祖细胞减少。
G-CSF通过降低骨髓SDF-1并下调HSPCs上CXCR4的表达来诱导HSPCs动员。