Kim Dong-Seok, Kim So-Young, Jeong Yun-Mi, Jeon Sang-Eun, Kim Myo-Kyoung, Kwon Sun-Bang, Park Kyoung-Chan
Research Division for Human Life Sciences, Seoul National University, Korea.
Biol Pharm Bull. 2006 Aug;29(8):1625-9. doi: 10.1248/bpb.29.1625.
Recently, we showed that a combination of indole-3-acetic acid (IAA) and horseradish peroxidase (HRP) produces hydrogen peroxide (H2O2), and that this leads to the apoptosis of G361 human melanoma cells. In the present study, flow cytometric analysis confirmed that H2O2 is involved the IAA/HRP-induced apoptotic process. We also found that IAA/HRP increases cell surface CD95 (Fas/APO-1) expression, and that this is blocked by catalase treatment. Furthermore, blocking CD95 with a neutralizing antibody significantly restored IAA/HRP-induced apoptosis. In addition, the IAA/HRP-induced activations of CD95 downstream molecules, i.e., caspase-8, Bid, and caspase-3, were also inhibited by catalase. Moreover, a caspase-8 inhibitor significantly blocked IAA/HRP-induced apoptosis. These results indicate that IAA/HRP-induced apoptosis involves a CD95-initiated death receptor signaling pathway initiated by hydrogen peroxide.
最近,我们发现吲哚 - 3 - 乙酸(IAA)和辣根过氧化物酶(HRP)的组合可产生过氧化氢(H₂O₂),并且这会导致G361人黑素瘤细胞凋亡。在本研究中,流式细胞术分析证实H₂O₂参与了IAA/HRP诱导的凋亡过程。我们还发现IAA/HRP可增加细胞表面CD95(Fas/APO - 1)的表达,而过氧化氢酶处理可阻断这种增加。此外,用中和抗体阻断CD95可显著恢复IAA/HRP诱导的凋亡。另外,过氧化氢酶也抑制了IAA/HRP诱导的CD95下游分子即半胱天冬酶 - 8、Bid和半胱天冬酶 - 3的激活。此外,半胱天冬酶 - 8抑制剂可显著阻断IAA/HRP诱导的凋亡。这些结果表明,IAA/HRP诱导的凋亡涉及由过氧化氢引发的CD95启动的死亡受体信号通路。