Efficacy of the coadministration of granulocyte colony-stimulating factor and stem cell factor in the activation of intrinsic cells after spinal cord injury in mice

被引:28
作者
Osada, Takahiro [2 ]
Watanabe, Masahiko [1 ]
Hasuo, Atsuhiro [1 ]
Imai, Masaaki [2 ]
Suyama, Kaori [1 ]
Sakai, Daisuke [1 ]
Kawada, Hiroshi [3 ]
Matsumae, Mitsunori [2 ]
Mochida, Joji [1 ]
机构
[1] Tokai Univ, Sch Med, Dept Orthopaed Surg, Kanagawa 2591193, Japan
[2] Tokai Univ, Sch Med, Dept Neurosurg, Kanagawa 2591193, Japan
[3] Tokai Univ, Sch Med, Dept Internal Med, Kanagawa 2591193, Japan
关键词
spinal cord injury; granulocyte colony-stimulating factor; stem cell factor; intrinsic cell; bone marrow-derived cell; microglia; oligodendrocyte progenitor cell; NEURAL STEM/PROGENITOR CELLS; PROMOTES FUNCTIONAL RECOVERY; FOCAL CEREBRAL-ISCHEMIA; MYOCARDIAL-INFARCTION; NEUROTROPHIC FACTOR; CONTUSION INJURY; PROGENITOR CELLS; PARAPLEGIC RATS; NERVOUS-SYSTEM; IN-VITRO;
D O I
10.3171/2010.4.SPINE09973
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Granulocyte colony-stimulating factor (G-CSF) is a hematopoietic cytokine that induces undifferentiated stem cells from the bone marrow (BM) into the peripheral blood. Stem cell factor (SCF) is also a hematopoietic cytokine that stimulates the differentiation and proliferation of neural stem cells and has neuroprotective effects. In cerebrally infarcted mice, the combination of G-CSF and SCF promotes the differentiation of BM-derived cells into neural cells, stimulates the proliferation of intrinsic neural stem cells, and improves motor function. The object of this study was to investigate the effects of these cytokines on BM stem cells, intrinsic cells, and motor function recovery in spinal cord injured mice. Methods. For marking BM-derived cells, the authors induced contusive spinal cord injury in mice transplanted with BM cells from green fluorescent protein (GFP)-transgenic mice after whole-body irradiation. These mice were treated with G-CSF and SCF in the subacute injury phase. Bromodeoxyuridine (BrdU) was injected into these mice to label proliferating cells. The cell numbers and phenotype of the BM-derived cells were evaluated, and the change in intrinsic cells (proliferation, accumulation, and differentiation) was noted using immunohistological analysis at 4 weeks postinjury (wpi). A behavior analysis was conducted until 12 wpi using the Basso, Beattie, Bresnahan locomotor rating scale. Results. In the SCF + G-CSF group, improvement in hindlimb motor function was significantly greater than in the SCF group, G-CSF group, and sham-treatment (vehicle) group after 8 wpi. At 4 wpi, the number of GFP+ BM-derived cells induced in the lesion did not significantly differ between groups. At 4 wpi, the authors evaluated perilesional GFP intrinsic spinal cord cells. The number of GFP and F4/80+ cells was significantly greater in the SCF + G-CSF group than in the other 3 groups. As compared with the sham group, the number of NG2+/BrdU+ cells was significantly increased in the SCF + G-CSF group. Conclusions. In this study, the combined administration of SCF and G-CSF in traumatic spinal cord injury not only improved motor function, but also induced the accumulation of intrinsic microglia and the active proliferation of intrinsic oligodendrocyte precursor cells. (DOI: 10.3171/2010.4.SPINE09973)
引用
收藏
页码:516 / 523
页数:8
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