Cao Xu-Qing, Arai Hiroyuki, Ren Yong-Ri, Oizumi Hideki, Zhang Ning, Seike Shiho, Furuya Tsuyoshi, Yasuda Toru, Mizuno Yoshikuni, Mochizuki Hideki
Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
J Neurochem. 2006 Nov;99(3):861-7. doi: 10.1111/j.1471-4159.2006.04125.x.
Granulocyte colony-stimulating factor (G-CSF) has been used for the treatment of neutropenia in hematologic disorders. The neuroprotective effects of G-CSF were reported in neurological disease models. In the present study, we examined whether G-CSF can protect dopaminergic neurons against MPTP-induced cell death in a mouse model of Parkinson's disease. Mice of one group were injected intraperitoneally with MPTP for five consecutive days, those of another group with MPTP and intraperitoneal G-CSF at 2 days and 1 day before the first MPTP injection, and 30 min before each MPTP injection, while control mice received saline injections. Immunohistochemistry, western blotting analysis, and HPLC were performed to evaluate damage of substantia nigra dopaminergic neurons and expression of Bcl-2 and Bax protein. MPTP induced dopaminergic cell death in the substantia nigra. G-CSF significantly prevented MPTP-induced loss of tyrosine hydroxylase-positive neurons (p < 0.05), increased Bcl-2 protein and decreased Bax protein expression. Our findings indicate that G-CSF provides neuroprotection against MPTP-induced cell death and this effect is mediated by increasing Bcl-2 expression levels and decreasing Bax expression levels in C57BL/6 mice.
粒细胞集落刺激因子(G-CSF)已被用于治疗血液系统疾病中的中性粒细胞减少症。在神经疾病模型中已报道了G-CSF的神经保护作用。在本研究中,我们检测了在帕金森病小鼠模型中G-CSF是否能保护多巴胺能神经元免受MPTP诱导的细胞死亡。一组小鼠连续5天腹腔注射MPTP,另一组在首次注射MPTP前2天和1天以及每次注射MPTP前30分钟腹腔注射MPTP和G-CSF,而对照小鼠注射生理盐水。进行免疫组织化学、蛋白质印迹分析和高效液相色谱法以评估黑质多巴胺能神经元的损伤以及Bcl-2和Bax蛋白的表达。MPTP诱导黑质中的多巴胺能细胞死亡。G-CSF显著预防了MPTP诱导的酪氨酸羟化酶阳性神经元的损失(p<0.05),增加了Bcl-2蛋白表达并降低了Bax蛋白表达。我们的研究结果表明,G-CSF对MPTP诱导的细胞死亡具有神经保护作用,并且这种作用是通过增加C57BL/6小鼠中Bcl-2表达水平和降低Bax表达水平来介导的。