Manevich Yefim, Fisher Aron B
Institute for Environmental Medicine, University of Pennsylvania Medical Center, Philadelphia, PA 19104, USA.
Free Radic Biol Med. 2005 Jun 1;38(11):1422-32. doi: 10.1016/j.freeradbiomed.2005.02.011.
Peroxiredoxin 6 (Prdx6), a bifunctional 25-kDa protein with both GSH peroxidase and phospholipase A2 activities, is the only mammalian 1-Cys member of the peroxiredoxin superfamily and is expressed in all major organs, with a particularly high level in lung. Prdx6 uses GSH as an electron donor to reduce H2O2 and other hydroperoxides including phospholipid hydroperoxides at approximately 5 micromol/mg protein/min with K1 approximately 3 x 10(6) M(-1) s(-1). Oxidation of the Cys47 to a sulfenic acid during catalysis requires piGST-catalyzed glutathionylation and reduction with GSH to complete the enzymatic cycle. Prdx6 stably overexpressed in cells protected against oxidative stress, whereas antisense treatment resulted in oxidant stress and apoptosis. Adenoviral-mediated overexpression of Prdx6 in mouse lungs protected against the toxicity of hyperoxia, whereas Prdx6-null mice were more sensitive to the effects of hyperoxia or paraquat. We postulate that Prdx6 functions in antioxidant defense mainly by facilitating repair of damaged cell membranes via reduction of peroxidized phospholipids. The PLA2 activity of Prdx6 is Ca2+ independent and maximal at acidic pH. Inhibition of PLA2 activity results in alterations of lung surfactant phospholipid synthesis and turnover. Thus, Prdx6, a unique mammalian peroxiredoxin, is an important antioxidant enzyme and has a major role in lung phospholipid metabolism.
过氧化物酶6(Prdx6)是一种具有谷胱甘肽过氧化物酶和磷脂酶A2活性的双功能25 kDa蛋白,是过氧化物酶超家族中唯一的哺乳动物1-半胱氨酸成员,在所有主要器官中均有表达,在肺中的表达水平尤其高。Prdx6以谷胱甘肽作为电子供体,以约5 μmol/mg蛋白/分钟的速度还原过氧化氢和其他氢过氧化物,包括磷脂氢过氧化物,其K1约为3×10(6) M(-1) s(-1)。催化过程中Cys47氧化为亚磺酸需要piGST催化的谷胱甘肽化并与谷胱甘肽还原以完成酶促循环。在细胞中稳定过表达的Prdx6可保护细胞免受氧化应激,而反义处理则导致氧化应激和细胞凋亡。腺病毒介导的Prdx6在小鼠肺中的过表达可保护小鼠免受高氧毒性,而Prdx6基因敲除小鼠对高氧或百草枯的影响更敏感。我们推测Prdx6在抗氧化防御中的作用主要是通过还原过氧化磷脂促进受损细胞膜的修复。Prdx6的磷脂酶A2活性不依赖于Ca2+,在酸性pH下活性最高。抑制磷脂酶A2活性会导致肺表面活性物质磷脂合成和周转的改变。因此,Prdx6作为一种独特的哺乳动物过氧化物酶,是一种重要的抗氧化酶,在肺磷脂代谢中起主要作用。