Wang Yan, Feinstein Sheldon I, Fisher Aron B
Institute for Environmental Medicine, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 19104-6068, USA.
J Cell Biochem. 2008 Jul 1;104(4):1274-85. doi: 10.1002/jcb.21703.
We evaluated the antioxidant role of peroxiredoxin 6 (Prdx6) in primary lung alveolar epithelial type II cells (AEC II) that were isolated from wild type (WT), Prdx6-/-, or Prdx6 transgenic (Tg) overexpressing mice and exposed to H(2)O(2) at 50-500 microM for 1-24 h. Expression of Prdx6 in Tg AEC II was sevenfold greater than WT. Prdx6 null AEC II exposed to H(2)O(2) showed concentration-dependent cytotoxicity indicated by decreased "live/dead" cell ratio, increased propidium iodide (PI) staining, increased annexin V binding, increased DNA fragmentation by TUNEL assay, and increased lipid peroxidation by diphenylpyrenylphosphine (DPPP) fluorescence. Compared to Prdx6 null cells, oxidant-mediated damage was significantly less in WT AEC II and was least in Prdx6 Tg cells. Thus, Prdx6 functions as an antioxidant enzyme in mouse AEC II. Prdx6 has been shown previously to reduce phospholipid hydroperoxides and we postulate that this activity is a major mechanism for the effectiveness of Prdx6 as an antioxidant enzyme.
我们评估了过氧化物还原酶6(Prdx6)在从野生型(WT)、Prdx6基因敲除小鼠(Prdx6-/-)或Prdx6转基因(Tg)过表达小鼠分离的原代肺II型肺泡上皮细胞(AEC II)中的抗氧化作用,并将这些细胞暴露于50-500微摩尔的过氧化氢(H₂O₂)中1-24小时。Tg AEC II中Prdx6的表达比WT高7倍。暴露于H₂O₂的Prdx6基因敲除的AEC II表现出浓度依赖性细胞毒性,表现为“活/死”细胞比例降低、碘化丙啶(PI)染色增加、膜联蛋白V结合增加、TUNEL法检测的DNA片段化增加以及二苯基芘基膦(DPPP)荧光检测的脂质过氧化增加。与Prdx6基因敲除细胞相比,WT AEC II中氧化剂介导的损伤明显减少,而在Prdx6 Tg细胞中最少。因此,Prdx6在小鼠AEC II中作为抗氧化酶发挥作用。先前已证明Prdx6可还原磷脂氢过氧化物,我们推测该活性是Prdx6作为抗氧化酶发挥作用的主要机制。