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首页> 外文期刊>Neuroscience Research: The Official Journal of the Japan Neuroscience Society >Administration of hematopoietic cytokines increases the expression of anti-inflammatory cytokine (IL-10) mRNA in the subacute phase after stroke.
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Administration of hematopoietic cytokines increases the expression of anti-inflammatory cytokine (IL-10) mRNA in the subacute phase after stroke.

机译:给予造血细胞因子可增加中风后亚急性期抗炎细胞因子(IL-10)mRNA的表达。

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摘要

We investigated the effect of the subcutaneous administration of hematopoietic cytokines, granulocyte colony-stimulating factor (G-CSF)+stem cell factor (SCF), on mRNA expression of tissue cytokines in the acute or subacute phase after focal ischemia in male C57 BL/6J mice. The expression of IL-10 mRNA was elevated at 4-14 days after occlusion when cytokines were given in the acute phase (days 1-10). The expression of IL-10 mRNA was markedly elevated at 14 days after occlusion, then remained high until 28 days when cytokines were given in the subacute phase (days 11-20). However, there were no significant changes in IL-6, TGF-beta1, TNF, G-CSF, SCF and iNOS expression following either acute- or subacute-phase treatment. Further, hematopoietic cytokine treatment in the subacute phase, but not in the acute phase, reduced ED1-positive microglia/macrophages in the infarcted brain. Our recent study showed that the subacute-phase treatment is effective for functional recovery, enhancing generation of neuronal cells from both bone-marrow-derived and neural stem/progenitor cells. Taken together, these results suggest that cytokine treatment in the subacute phase may provide a favorable microenvironment for neurogenesis after ischemic stroke through the up-regulation of IL-10.
机译:我们调查了皮下注射造血细胞因子,粒细胞集落刺激因子(G-CSF)+干细胞因子(SCF)对雄性C57 BL /急性或亚急性期组织细胞因子mRNA表达的影响6J小鼠。当在急性期(第1-10天)给予细胞因子时,在闭塞后4-14天IL-10 mRNA的表达升高。 IL-10 mRNA的表达在闭塞后14天明显升高,然后保持高水平,直到亚急性期(第11至20天)给予细胞因子的28天为止。然而,急性或亚急性期治疗后,IL-6,TGF-β1,TNF,G-CSF,SCF和iNOS表达无明显变化。此外,在亚急性期而不是急性期的造血细胞因子治疗减少了梗死脑中ED1阳性的小胶质细胞/巨噬细胞。我们最近的研究表明,亚急性期治疗可有效恢复功能,增强来自骨髓和神经干/祖细胞的神经元细胞的生成。综上所述,这些结果表明亚急性期的细胞因子治疗可通过上调IL-10来为缺血性中风后的神经发生提供有利的微环境。

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