Hung W C, Chang H C, Chuang L Y
School of Technology for Medical Sciences, Kaohsiung Medical College, Taiwan, Republic of China.
Biochem J. 1999 Feb 15;338 ( Pt 1)(Pt 1):161-6.
Sphingosine and other long-chain bases (including sphinganine, dimethylsphingosine and stearylamine), but not octylamine (a short-chain analogue of sphinganine), induced apoptosis in Hep3B hepatoma cells. Because both D- and L-erythrosphingosine and stearylamine exert potent apoptotic effects on Hep3B cells, it is possible that these long-chain bases may activate apoptosis by inhibiting protein kinase C (PKC) activity. However, pretreatment with the PKC activator PMA could not rescue cells from apoptosis triggered by long-chain bases. Therefore the involvement of PKC in this apoptotic process requires further characterization. We also investigated whether these long-chain bases might be metabolized into ceramide in order to elicit their apoptotic action. We found that long-chain bases acted independently of ceramide in the induction of apoptosis, since addition of fumonisin B1, a fungal agent which effectively inhibits ceramide synthesis from sphingosine, did not protect against apoptosis. Additionally, we found that sphingosine-induced apoptosis was accompanied by activation of caspases. The functional role of caspases in this apoptotic process was examined by using specific caspase inhibitors. The general caspase inhibitor benzyloxycarbonyl-Val-Ala-Asp fluoromethyl ketone, which exhibits a broad specificity for caspase-family proteases, effectively blocked sphingosine-induced apoptosis. Furthermore, our results indicate that caspase-3-like proteases, but not caspase-1, are activated during apoptosis triggered by sphingosine. Enhancement of caspase-3-like activity and cleavage of poly(ADP-ribose) polymerase, an in vivo substrate for caspase-3, was clearly demonstrated in sphingosine-treated Hep3B cells. Considered together, these results suggest that caspase-3-like proteases participate in apoptotic cell death induced by sphingosine.
鞘氨醇和其他长链碱(包括二氢鞘氨醇、二甲基鞘氨醇和硬脂胺)可诱导Hep3B肝癌细胞凋亡,但辛胺(二氢鞘氨醇的短链类似物)则不能。由于D-和L-赤藓糖型鞘氨醇以及硬脂胺对Hep3B细胞均有强大的凋亡作用,因此这些长链碱可能通过抑制蛋白激酶C(PKC)活性来激活凋亡。然而,用PKC激活剂佛波酯(PMA)预处理并不能使细胞免于长链碱引发的凋亡。因此,PKC在这一凋亡过程中的作用还需要进一步明确。我们还研究了这些长链碱是否可能代谢生成神经酰胺以引发其凋亡作用。我们发现长链碱在诱导凋亡过程中独立于神经酰胺发挥作用,因为添加伏马菌素B1(一种可有效抑制鞘氨醇合成神经酰胺的真菌制剂)并不能防止细胞凋亡。此外,我们发现鞘氨醇诱导的凋亡伴随着半胱天冬酶的激活。通过使用特异性半胱天冬酶抑制剂来研究半胱天冬酶在这一凋亡过程中的功能作用。对半胱天冬酶家族蛋白酶具有广泛特异性的通用半胱天冬酶抑制剂苄氧羰基-Val-Ala-Asp氟甲基酮可有效阻断鞘氨醇诱导的凋亡。此外,我们的结果表明,在鞘氨醇引发的凋亡过程中,激活的是类半胱天冬酶-3蛋白酶,而非半胱天冬酶-1。在经鞘氨醇处理的Hep3B细胞中,类半胱天冬酶-3活性增强以及聚(ADP-核糖)聚合酶(半胱天冬酶-3在体内的底物)的裂解均得到了明确证实。综合来看,这些结果表明类半胱天冬酶-3蛋白酶参与了鞘氨醇诱导的细胞凋亡死亡过程。