Imai H, Narashima K, Arai M, Sakamoto H, Chiba N, Nakagawa Y
School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan.
J Biol Chem. 1998 Jan 23;273(4):1990-7. doi: 10.1074/jbc.273.4.1990.
The overexpression of phospholipid hydroperoxide glutathione peroxidase (PHGPx) by RBL-2H3 cells was used as the basis for an investigation of the effects of PHGPx on the formation of leukotrienes. The rates of production of leukotriene C4 (LTC4) and leukotriene B4 (LTB4) in cells that overexpressed PHGPx were 8 times lower than those in a control line of cells. The reduction in rates of production of leukotrienes apparently resulted from the increase in the PHGPx activity since control rates of formation of leukotrienes could be achieved in PHGPx-overexpressing cells upon inhibition of PHGPx activity by diethyl malate. The conversion of radioactively labeled arachidonic acid to intermediates in the lipoxygenase pathway, such as 5-hydroxyeicosatetraenoic acid (5-HETE), LTC4, and LTB4, was strongly inhibited in PHGPx-overexpressing cells that had been prelabeled with [14C]arachidonic acid. PHGPx apparently inactivated the 5-lipoxygenase that catalyzed the conversion of arachidonic acid to 5-hydroperoxyeicosatetraenoic acid (5-HPETE) since 5-HPETE is a common precursor of 5-HETE, LTC4, and LTB4. The rates of formation of LTC4 and LTB4 in PHGPx-overexpressing cells returned to control rates upon the addition of a small amount of 12-HPETE. Flow cytometric analysis revealed that the rapid burst of formation of lipid hydroperoxides induced by A23187 was suppressed in PHGPx-overexpressing cells as compared with the control lines of cells. Subcellular fractionation analysis showed that the amount of PHGPx associated with nuclear fractions from PHGPx-overexpressing cells was 3.5 times higher than that from the control line of cells. These results indicate that PHGPx might be involved in inactivation of 5-lipoxygenase via reductions in levels of the fatty acid hydroperoxides that are required for the full activation of 5-lipoxygenase. Thus, in addition to its role as an antioxidant enzyme, PHGPx appears to have a novel function as a modulator of the production of leukotrienes.
RBL - 2H3细胞中磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPx)的过表达被用作研究PHGPx对白三烯形成影响的基础。过表达PHGPx的细胞中白三烯C4(LTC4)和白三烯B4(LTB4)的产生速率比对照细胞系低8倍。白三烯产生速率的降低显然是由于PHGPx活性的增加,因为在用苹果酸二乙酯抑制PHGPx活性后,过表达PHGPx的细胞中白三烯的对照形成速率可以实现。在用[14C]花生四烯酸预标记的过表达PHGPx的细胞中,放射性标记的花生四烯酸向脂氧合酶途径中间体的转化,如5 - 羟基二十碳四烯酸(5 - HETE)、LTC4和LTB4,受到强烈抑制。PHGPx显然使催化花生四烯酸转化为5 - 氢过氧二十碳四烯酸(5 - HPETE)的5 - 脂氧合酶失活,因为5 - HPETE是5 - HETE、LTC4和LTB4的共同前体。加入少量12 - HPETE后,过表达PHGPx的细胞中LTC4和LTB4的形成速率恢复到对照速率。流式细胞术分析表明,与对照细胞系相比,过表达PHGPx的细胞中由A23187诱导的脂质氢过氧化物的快速爆发受到抑制。亚细胞分级分离分析表明,过表达PHGPx的细胞中与核级分相关的PHGPx量比对照细胞系高3.5倍。这些结果表明,PHGPx可能通过降低5 - 脂氧合酶完全激活所需的脂肪酸氢过氧化物水平而参与5 - 脂氧合酶的失活。因此,除了作为抗氧化酶的作用外,PHGPx似乎还具有作为白三烯产生调节剂的新功能。