Yui Satoru, Kudo Tomoya, Hodono Kazumi, Mimaki Yoshihiro, Kuroda Minpei, Sashida Yutaka, Yamazaki Masatoshi
Faculty of Pharmaceutical Sciences, Teikyo University, 199-0195 Kanagawa, Japan.
Mediators Inflamm. 2003 Jun;12(3):157-66. doi: 10.1080/0962935031000134879.
Since the growth state of macrophages in local pathological sites is considered a factor that regulates the processes of many disease, such as tumors, inflammation, and atherosclerosis, the substances that regulate macrophage growth or survival may be useful for disease control. We previously reported that securiosides A and B, novel triterpene saponins, exerted macrophage-oriented cytotoxicity in the presence of a L-cell-conditioned medium containing macrophage colony-stimulating factor (M-CSF), while the compounds did not exhibit an effect on macrophages in the absence of the growth-stimulating factors.
This study was undertaken to characterize the growth-inhibitory and the apoptosis-inducing activities of securioside B, focusing on the effects of the macrophage-growth factor(s), and to examine the implication of a mitochondria pathway in apoptosis induction.
The effect of securioside B on a murine macrophage cell line (BAC1.2F5) was examined by MTT assay and lactose dehydrogenase release assay in the presence of L-cell-conditioned medium, M-CSF, or granulocyte-macrophage CSF (GM-CSF).
Securioside B inhibited the growth of the cells stimulated by recombinant M-CSF or GM-CSF, but it scarcely induced cytolysis of the cells under the same conditions. Moreover, securioside B did not induce cell death when the compound only was added to the cells. On the other hand, the compound extensively induced apoptotic cell death in the presence of L-cell-conditioned medium, suggesting that apoptosis induction by securioside B requires the additional factor(s) present in L-cell-conditioned medium. Securioside B plus L-cell-conditioned medium induced the activation of caspase-3 and caspase-9, but not caspase-8. In addition, cytochrome c release from the mitochondria into the cytosol, and disrupted mitochondria membrane potential, was also observed in the apoptotic BAC1.2F5 cells.
These data suggest that securioside B has growth-inhibitory activity against growth factor-stimulated macrophages, and that it induces apoptotic macrophage death through the activation of a mitochondrial pathway in the presence of L-cell-conditioned medium.
由于巨噬细胞在局部病理部位的生长状态被认为是调节许多疾病进程的一个因素,如肿瘤、炎症和动脉粥样硬化,因此调节巨噬细胞生长或存活的物质可能对疾病控制有用。我们之前报道过,新型三萜皂苷securiosides A和B在含有巨噬细胞集落刺激因子(M-CSF)的L细胞条件培养基存在的情况下,对巨噬细胞具有细胞毒性,而在没有生长刺激因子的情况下,这些化合物对巨噬细胞没有影响。
本研究旨在表征securioside B的生长抑制和凋亡诱导活性,重点关注巨噬细胞生长因子的作用,并研究线粒体途径在凋亡诱导中的意义。
在L细胞条件培养基、M-CSF或粒细胞-巨噬细胞集落刺激因子(GM-CSF)存在的情况下,通过MTT法和乳酸脱氢酶释放试验检测securioside B对小鼠巨噬细胞系(BAC1.2F5)的影响。
Securioside B抑制重组M-CSF或GM-CSF刺激的细胞生长,但在相同条件下几乎不诱导细胞溶解。此外,当仅将该化合物添加到细胞中时,securioside B不会诱导细胞死亡。另一方面,在L细胞条件培养基存在的情况下,该化合物广泛诱导凋亡细胞死亡,这表明securioside B诱导凋亡需要L细胞条件培养基中存在的其他因子。Securioside B加L细胞条件培养基诱导caspase-3和caspase-9激活,但不诱导caspase-8激活。此外,在凋亡的BAC1.2F5细胞中也观察到细胞色素c从线粒体释放到细胞质中,以及线粒体膜电位的破坏。
这些数据表明,securioside B对生长因子刺激的巨噬细胞具有生长抑制活性,并且在L细胞条件培养基存在的情况下,它通过激活线粒体途径诱导巨噬细胞凋亡死亡。