Morita Yuko, Takizawa Shunya, Kamiguchi Hiroshi, Uesugi Tsuyoshi, Kawada Hiroshi, Takagi Shigeharu
Division of Neurology, Department of Internal Medicine, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
Neurosci Res. 2007 Aug;58(4):356-60. doi: 10.1016/j.neures.2007.04.006. Epub 2007 Apr 19.
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.
我们研究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/6J小鼠局灶性缺血后急性期或亚急性期组织细胞因子mRNA表达的影响。在急性期(第1 - 10天)给予细胞因子时,闭塞后4 - 14天白细胞介素10(IL-10)mRNA的表达升高。在亚急性期(第11 - 20天)给予细胞因子时,闭塞后14天IL-10 mRNA的表达显著升高,然后一直保持高水平直至28天。然而,急性期或亚急性期治疗后,白细胞介素6(IL-6)、转化生长因子β1(TGF-β1)、肿瘤坏死因子(TNF)、G-CSF、SCF和诱导型一氧化氮合酶(iNOS)的表达均无显著变化。此外,亚急性期而非急性期的造血细胞因子治疗可减少梗死脑中ED1阳性的小胶质细胞/巨噬细胞。我们最近的研究表明,亚急性期治疗对功能恢复有效,可增强骨髓源性和神经干细胞/祖细胞产生神经元细胞的能力。综上所述,这些结果表明亚急性期的细胞因子治疗可能通过上调IL-10为缺血性中风后的神经发生提供有利的微环境。