Isoyama Naohito, Takai Kimio, Tsuchida Masahiro, Matsumura Masafumi, Naito Katsusuke
Department of Urology, Yamaguchi University School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi 755-8505, Japan.
Transpl Immunol. 2006 Apr;15(4):265-71. doi: 10.1016/j.trim.2006.02.004. Epub 2006 Mar 27.
FTY720, a novel immunomodulator with the potential to improve immunosuppressive therapy after organ transplantation, is currently under clinical investigation. FTY720 drastically decreases blood lymphocytes, especially T cells, accelerating lymphocyte homing to secondary lymphoid organs. However, its immunosuppressive effects remain unknown. We investigated these effects in rat thymocytes. Rats were intramuscularly injected with 10mg/kg/day FTY720 or saline for 7days. Thymuses were removed on days 0, 1, 3, 5, 7 and 14 after treatment. Three-color analysis was performed with a flow cytofluorometer. Apoptotic nuclei in the tissue sections were identified by TUNEL. Genomic DNA was then extracted and samples were electrophoresed on 2.0% agarose gel. FTY720 reduced the total number of thymocytes and, with time, significantly reduced the percentage of CD4+8+ TCRalphabeta(negative/low) thymocytes. Light microscopy of thymuses of FTY720-treated rats revealed obvious reductions in the size of the cortical region. TUNEL analysis showed that FTY720 induced thymocyte apoptosis in the cortical region. Furthermore, DNA fragmentation was observed in thymocytes treated with FTY720, indicating thymocyte apoptosis. FTY720 reduced the number of CD4+8+ thymocytes before TCRalphabeta expression resulting in impaired thymocyte differentiation and maturation. This might be an immunosuppressive effect of FTY720.
FTY720是一种新型免疫调节剂,具有改善器官移植后免疫抑制治疗的潜力,目前正处于临床研究阶段。FTY720能大幅减少血液中的淋巴细胞,尤其是T细胞,加速淋巴细胞归巢至次级淋巴器官。然而,其免疫抑制作用尚不清楚。我们在大鼠胸腺细胞中研究了这些作用。将大鼠肌肉注射10mg/kg/天的FTY720或生理盐水,持续7天。在治疗后的第0、1、3、5、7和14天取出胸腺。用流式细胞荧光仪进行三色分析。通过TUNEL法鉴定组织切片中的凋亡细胞核。然后提取基因组DNA,并将样品在2.0%琼脂糖凝胶上进行电泳。FTY720减少了胸腺细胞的总数,并且随着时间的推移,显著降低了CD4+8+ TCRαβ(阴性/低表达)胸腺细胞的百分比。对接受FTY720治疗的大鼠胸腺进行光学显微镜检查发现,皮质区域的大小明显减小。TUNEL分析表明,FTY720诱导皮质区域的胸腺细胞凋亡。此外,在用FTY720处理的胸腺细胞中观察到DNA片段化,表明胸腺细胞凋亡。FTY720在TCRαβ表达之前减少了CD4+8+胸腺细胞的数量,导致胸腺细胞分化和成熟受损。这可能是FTY720的一种免疫抑制作用。