首页> 外文期刊>Biochemistry and Biophysics Reports >Bax and caspases regulate increased production of mitochondria-derived reactive species in neuronal apoptosis: LACK of A role for depletion of cytochrome c from the mitochondrial electron transport chain
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Bax and caspases regulate increased production of mitochondria-derived reactive species in neuronal apoptosis: LACK of A role for depletion of cytochrome c from the mitochondrial electron transport chain

机译:Bax和胱氨酸蛋白酶调节神经细胞凋亡中线粒体来源的反应性物种的生产增加:A的缺乏对线粒体电子传输链中细胞色素c耗竭的作用

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A Bax-dependent increase of reactive oxygen species (ROS) and other reactive species (RS) occurs after withdrawing NGF from mouse sympathetic neurons in cell culture. Possible mechanisms underlying the increased ROS/RS are leakage of electrons from the mitochondrial electron transport chain secondary to caspase cleavage of respiratory complexes or leakage secondary to depletion of cytochrome c from the chain. We previously demonstrated that deletion of Bax or caspase 3 from these cells reduces ROS/RS production to near baseline levels indicating a central role for both Bax and caspase 3 in generating the ROS/RS. Here we depleted cytochrome c to a similar level in neurons from wild type and bax hemizygous or knockout mice by NGF withdrawal or treatment with H 2 O 2 . Death was prevented with a caspase inhibitor that caused a partial reduction of ROS/RS levels but did not completely prevent the ROS/RS increase. ROS/RS was highest in bax wild-type cells, lowest in bax knockout cells, and at an intermediate level in the bax hemizygous cells. These and our previous findings indicate that Bax and caspase 3 are necessary for the increased ROS/RS after withdrawing NGF from these cells and that little or none of the increased ROS/RS are secondary to a depletion of cytochrome c from the electron transport chain. Highlights ? Bax lies upstream of all increased production of ROS by mitochondria in NGF-deprived sympathetic neurons. ? The broad-spectrum caspase inhibitor BAF blocks some but not all increased ROS after NGF withdrawal. ? Caspase 3 deletion blocks almost all of the increased ROS after NGF withdrawal suggesting that BAF does not block all caspase activity or that it has non-specific pro-oxidant effects. ? Depletion of cytochrome c from the electron transport chain contributes little or nothing to increased ROS after NGF withdrawal.
机译:从细胞培养的小鼠交感神经元中提取NGF后,活性氧(ROS)和其他活性物质(RS)的Bax依赖性增加。 ROS / RS升高的可能机制是继呼吸复合物的半胱天冬酶裂解之后,继发于线粒体电子转运链的电子泄漏或继而从细胞色素耗尽导致的继发泄漏。我们以前证明了从这些细胞中删除Bax或caspase 3可以将ROS / RS的产生降低到接近基线水平,这表明Bax和caspase 3都在产生ROS / RS中起着核心作用。在这里,我们通过NGF撤除或用H 2 O 2处理将野生型和bax半合子或敲除小鼠的神经元中的细胞色素c消耗至相似水平。用半胱天冬酶抑制剂预防了死亡,该抑制剂引起ROS / RS水平的部分降低,但并未完全阻止ROS / RS的升高。 ROS / RS在bax野生型细胞中最高,在bax基因敲除细胞中最低,在bax半合子细胞中处于中等水平。这些以及我们先前的发现表明,从这些细胞中抽出NGF后,Bax和caspase 3对于ROS / RS的增加是必需的,并且增加的ROS / RS很少或没有继发于电子传输链中细胞色素c的消耗。强调 ? Bax处于NGF缺乏的交感神经元中线粒体所有ROS产生增加的上游。 ? NGF撤药后,广谱半胱天冬酶抑制剂BAF可以阻断部分但不是全部增加的ROS。 ?在NGF撤除后,胱天蛋白酶3缺失几乎阻止了所有增加的ROS,这表明BAF不能阻断所有胱天蛋白酶活性或具有非特异性的促氧化剂作用。 ? NGF撤离后,电子传输链中细胞色素c的耗竭对ROS的增加几乎没有贡献。

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