Lacza Zsombor, Snipes James A, Zhang Jie, Horváth Eszter M, Figueroa Jorge P, Szabó Csaba, Busija David W
Department of Physiology/Pharmacology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC, USA.
Free Radic Biol Med. 2003 Nov 15;35(10):1217-28. doi: 10.1016/s0891-5849(03)00510-0.
Recent studies indicated that there is a distinct mitochondrial nitric oxide synthase (mtNOS) enzyme, which may be identical to the other known NOS isoforms. We investigated the possible involvement of the endothelial, the neuronal, and the inducible NOS isoforms (eNOS, nNOS, iNOS, respectively) in mitochondrial NO production. Mouse liver mitochondria were prepared by Percoll gradient purification from wild-type and NOS knockout animals. NOS activity was measured by the arginine conversion assay, NO production of live mitochondria was visualized by the fluorescent probe DAF-FM with confocal microscopy and measured with flow cytometry. Western blotting or immunoprecipitation was performed with 12 different anti-NOS antibodies. Mitochondrial NOS was purified by arginine, 2,5 ADP and calmodulin affinity columns. We observed NO production and NOS activity in mitochondria, which was not attenuated by classic NOS inhibitors. We also detected low amounts of eNOS protein in the mitochondria, however, NO production and NOS activity were intact in eNOS knockout animals. Neither nNOS nor iNOS were present in the mitochondria. Furthermore, we could not find mitochondrial targeting signals in the sequences of either NOS proteins. Taken together, the presented data do not support the hypothesis that any of the known NOS enzymes are present in the mitochondria in physiologically relevant levels.
最近的研究表明,存在一种独特的线粒体一氧化氮合酶(mtNOS),它可能与其他已知的一氧化氮合酶同工型相同。我们研究了内皮型、神经元型和诱导型一氧化氮合酶同工型(分别为eNOS、nNOS、iNOS)在线粒体一氧化氮生成中的可能作用。通过Percoll梯度离心法从野生型和一氧化氮合酶基因敲除动物中制备小鼠肝脏线粒体。通过精氨酸转化试验测量一氧化氮合酶活性,利用荧光探针DAF-FM通过共聚焦显微镜观察活线粒体的一氧化氮生成情况,并通过流式细胞术进行测量。用12种不同的抗一氧化氮合酶抗体进行蛋白质印迹或免疫沉淀。通过精氨酸、2,5-二磷酸腺苷和钙调蛋白亲和柱纯化线粒体一氧化氮合酶。我们观察到线粒体中有一氧化氮生成和一氧化氮合酶活性,而经典的一氧化氮合酶抑制剂并不能减弱这种现象。我们还在线粒体中检测到少量的eNOS蛋白,然而,在eNOS基因敲除动物中,一氧化氮生成和一氧化氮合酶活性仍然完好。线粒体中既不存在nNOS也不存在iNOS。此外,我们在任何一种一氧化氮合酶蛋白序列中都未发现线粒体靶向信号。综上所述,目前的数据并不支持任何一种已知的一氧化氮合酶在生理相关水平存在于线粒体中的假说。