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首页> 外文期刊>The international journal of biochemistry and cell biology >Augmenter of liver regeneration, a protective factor against ROS-induced oxidative damage in muscle tissue of mitochondrial myopathy affected patients
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Augmenter of liver regeneration, a protective factor against ROS-induced oxidative damage in muscle tissue of mitochondrial myopathy affected patients

机译:肝再生的增强剂,一种防止ROS引起的线粒体肌病患者肌肉组织氧化损伤的保护因子

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Mitochondria-related myopathies (MM) are a group of different diseases defined by a varying degree of dysfunctions of the mitochondrial respiratory chain which leads to reactive oxygen species (ROS) generation followed by oxidative stress and cellular damage. In mitochondrial myopathy muscle tissue an overexpression of antioxidant enzymes has been documented probably as an attempt to counteract the free radical generation. We previously documented, in human non-pathological muscle fibres, the expression of the augmenter of liver regeneration (ALR), a sulfhydryl oxidase enzyme, whose presence is related to the mitochondria; indeed it has been demonstrated that ALR mainly localizes in the mitochondrial inter-membrane space. Furthermore we reported, in different experimental models, in vivo and in vitro, the anti-apoptotic and anti-oxidative capacities of ALR, achieved by up-regulating Bcl-2 anti-apoptotic family factors and the anti-apoptotic/anti-oxidative secretory isoform of clusterin (sClu). With the present study we aimed to determine ALR, Bcl-2 protein, clusterin and ROS expression in muscle tissue biopsies from MM-affected patients. Non-pathological muscle tissue was used as control. Enzymatic, histochemical, immunohistochemical and immune electron microscopy techniques were performed. The data obtained revealed in MM-derived muscle tissue, compared to non-pathological tissue, the over-expression of ROS, ALR and Bcl-2 and the induction of the nuclear, pro-apoptotic, isoform of clusterin (nCLU).
机译:线粒体相关性肌病(MM)是一组不同的疾病,由线粒体呼吸链功能障碍的不同程度定义,这些功能障碍导致活性氧(ROS)生成,继之以氧化应激和细胞损伤。在线粒体肌病的肌肉组织中,抗氧化酶的过表达可能已被证明是抵消自由基生成的一种尝试。我们先前在人类非病理性肌纤维中记录了肝脏再生增强剂(ALR)(一种巯基氧化酶)的表达,其存在与线粒体有关。确实已经证明ALR主要定位于线粒体膜间空间。此外,我们还报道了在不同的实验模型中,体内和体外通过上调Bcl-2抗凋亡家族因子和抗凋亡/抗氧化分泌而获得的ALR的抗凋亡和抗氧化能力簇蛋白的同种型(sClu)。通过本研究,我们旨在确定受MM影响的患者的肌肉组织活检中的ALR,Bcl-2蛋白,簇蛋白和ROS表达。非病理性肌肉组织用作对照。进行了酶促,组织化学,免疫组织化学和免疫电子显微镜技术。与非病理性组织相比,在MM来源的肌肉组织中获得的数据表明,ROS,ALR和Bcl-2的过度表达以及核素,促凋亡性簇蛋白(nCLU)的诱导。

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