Yaguchi Masae, Ohta Shigeki, Toyama Yoshiaki, Kawakami Yutaka, Toda Masahiro
Neuroimmunology Research Group, Keio University School of Medicine, Tokyo, Japan.
J Neurosci Res. 2008 Jul;86(9):1972-80. doi: 10.1002/jnr.21658.
We have previously reported that the transplantation of dendritic cells (DCs) brings about functional recovery after spinal cord injury in mice through the activation of endogenous microglia/macrophages and neural stem/progenitor cells. In this study, the effect of interleukin-12 (IL-12), which is secreted from DCs, was evaluated for the treatment of spinal cord injury in mice. Administration of IL-12 into the injured site significantly increased the number of activated microglia/macrophages and DCs as well as the expression of brain-derived neurotrophic factor surrounding the lesion site. Immunohistochemical analyses showed that de novo neurogenesis and remyelination were induced by IL-12 treatment. Furthermore, an open field test using Basso-Beattie-Brenham scoring revealed a significant improvement of locomotor function in mice treated with IL-12. These results suggest that IL-12 administration into the injured spinal cord results in a functional recovery through the activation of microglia/macrophages and DCs.
我们之前曾报道,树突状细胞(DCs)移植可通过激活内源性小胶质细胞/巨噬细胞和神经干/祖细胞,使小鼠脊髓损伤后实现功能恢复。在本研究中,我们评估了DCs分泌的白细胞介素-12(IL-12)对小鼠脊髓损伤治疗的效果。将IL-12注入损伤部位可显著增加活化的小胶质细胞/巨噬细胞和DCs的数量,以及损伤部位周围脑源性神经营养因子的表达。免疫组织化学分析表明,IL-12治疗可诱导新生神经发生和髓鞘再生。此外,使用Basso-Beattie-Brenham评分进行的旷场试验显示,接受IL-12治疗的小鼠运动功能有显著改善。这些结果表明,向损伤的脊髓注射IL-12可通过激活小胶质细胞/巨噬细胞和DCs实现功能恢复。