Kim C H, Pelus L M, White J R, Broxmeyer H E
Department of Microbiology/Immunology, Indiana University School of Medicine, Indianapolis 46202, USA.
J Immunol. 1998 Sep 1;161(5):2580-5.
Chemoattractants are potential factors influencing cell migration. Stromal cell-derived factor-1, a CXC chemokine, is the only chemokine reported to have chemotactic activity for hemopoietic progenitor cells (HPC). We report in this work another chemokine of the CC subfamily, which is chemotactic for HPC. Macrophage-inflammatory protein (MIP)-3 beta/EBI1-ligand chemokine/CK beta-11 attracted bone marrow and cord blood CD34+ cells. In contrast to stromal cell-derived factor-1, which attracts multiple types of HPC, MIP-3beta attracted mainly CFU granulocyte macrophage, but not other HPC such as burst-forming unit erythrocyte or CFU granulocyte, erythrocyte, macrophage, and megakaryocyte. Chemoattracted CD34+ cells formed CFU granulocyte macrophage-like colonies, which were morphologically determined as large macrophages. These progenitors were selectively responsive to stimulation by macrophage CSF, demonstrating that MIP-3 beta attracts macrophage progenitors. Expression of CCR7, the receptor for MIP-3 beta, was detected at a mRNA level in the attracted CD34+ cells as well as input CD34+HPC. Expression of MIP-3 beta mRNA was not constitutive, but was inducible in bone marrow stromal cells by inflammatory agents such as bacterial LPS, IFN-gamma, and TNF-alpha. Taken together, our findings suggest that MIP-3 beta is expressed in the bone marrow environment after induction with certain inflammatory cytokines and LPS, and may play a role in trafficking of macrophage progenitors in and out of the bone marrow in inflammatory conditions.
趋化因子是影响细胞迁移的潜在因素。基质细胞衍生因子-1是一种CXC趋化因子,是唯一被报道对造血祖细胞(HPC)具有趋化活性的趋化因子。我们在这项研究中报告了CC亚家族的另一种趋化因子,它对HPC具有趋化作用。巨噬细胞炎性蛋白(MIP)-3β/EBI1配体趋化因子/CKβ-11可吸引骨髓和脐血中的CD34+细胞。与吸引多种类型HPC的基质细胞衍生因子-1不同,MIP-3β主要吸引CFU粒巨噬细胞,而不吸引其他HPC,如爆式红细胞集落形成单位或CFU粒、红、巨噬和巨核细胞。被趋化的CD34+细胞形成了CFU粒巨噬细胞样集落,形态学上确定为大巨噬细胞。这些祖细胞对巨噬细胞集落刺激因子的刺激有选择性反应,表明MIP-3β吸引巨噬细胞祖细胞。在被趋化的CD34+细胞以及输入的CD34+HPC中,在mRNA水平检测到MIP-3β的受体CCR7的表达。MIP-3βmRNA的表达不是组成性的,而是可被细菌脂多糖、干扰素-γ和肿瘤坏死因子-α等炎性因子在骨髓基质细胞中诱导表达。综上所述,我们的研究结果表明,MIP-3β在某些炎性细胞因子和脂多糖诱导后在骨髓环境中表达,可能在炎症条件下巨噬细胞祖细胞进出骨髓的运输中起作用。