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首页> 外文期刊>Biochimica et biophysica acta. Molecular basis of disease: BBA >Age-related alterations in expression of apoptosis regulatory proteins and heat shock proteins in rat skeletal muscle
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Age-related alterations in expression of apoptosis regulatory proteins and heat shock proteins in rat skeletal muscle

机译:大鼠骨骼肌细胞凋亡调控蛋白和热休克蛋白表达的年龄相关变化

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Aging of skeletal muscle is often accompanied by muscle atrophy and it appears that apoptosis plays an important role in this process. The detailed mechanism(s) is not completely understood, however. In this study, we examined expression of the apoptosis regulatory proteins as well as the heat shock proteins, which have been shown to modulate the apoptotic process in certain cell types, in order to more completely elucidate apoptotic signaling in aged skeletal muscle. To more specifically identify alterations that are likely to be the result of aging, we compared 16-month-old middle-aged (MD) and 29-month-old senescent (SE) male Fischer 344 x Brown Norway rats in our study. Our results show that the degree of DNA laddering was higher in SE compared to MD rats. Using total tissue homogenates we examined the level of expression of several apoptosis-related proteins in two categories: mitochondria-associated proteins and caspases. Of the mitochondria-associated proteins, the levels of p53 showed a significant increase in SE compared to MD rats. There was also a significant increase in the expression of Bax, Bcl-2 and Apaf-1 in SE rats over that of MD rats; cytochrome c and AIF levels remained unchanged, however. Regarding the caspases, there were increases in the levels of pro-caspases-12 and -7 and cleaved caspase-9, although the levels of pro- and cleaved caspase-3 as well as cleaved caspase-12 remained unchanged. Furthermore, our results showed significant increases in HSP27, HSP60, and the inducible HSP70. These data show that in rat skeletal muscle increased apoptosis occurs between middle-age and senescence, indicating an aging-related increase in apoptosis in skeletal muscle. The involvement of different apoptotic pathways in the aging process is suggested by the selective alterations in the apoptosis regulatory proteins. The increased expression of the HSPs suggests a relationship between HSPs and the aging-related apoptotic process. (c) 2005 Elsevier B.V. All rights reserved.
机译:骨骼肌的衰老通常伴随着肌肉萎缩,并且似乎凋亡在这一过程中起着重要的作用。但是,尚未完全理解详细的机制。在这项研究中,我们检查了凋亡调节蛋白以及热休克蛋白的表达,这些蛋白已被证明可以调节某些细胞类型的凋亡过程,以便更彻底地阐明老年骨骼肌中的凋亡信号。为了更具体地识别可能是衰老的变化,我们在研究中比较了16个月大的中年(MD)和29个月大的衰老(SE)雄性Fischer 344 x Brown Norway大鼠。我们的结果表明,与MD大鼠相比,SE中的DNA阶梯化程度更高。使用组织匀浆,我们检查了两类与凋亡相关的蛋白质的表达水平:线粒体相关的蛋白质和胱天蛋白酶。与MD大鼠相比,在线粒体相关蛋白中,p53的水平显示SE显着增加。 SE大鼠中Bax,Bcl-2和Apaf-1的表达也显着高于MD大鼠。然而,细胞色素c和AIF水平保持不变。关于半胱天冬酶,尽管半胱天冬酶原和裂解的caspase-3水平以及裂解的半胱天冬酶12的水平保持不变,但是半胱天冬酶12和-7和裂解的半胱天冬酶9的水平增加。此外,我们的结果显示HSP27,HSP60和诱导型HSP70显着增加。这些数据表明,大鼠骨骼肌细胞凋亡的增加发生在中年至衰老之间,表明骨骼肌细胞凋亡的衰老相关性增加。凋亡调节蛋白的选择性改变提示不同的凋亡途径参与衰老过程。 HSP的表达增加表明HSP与衰老相关的凋亡过程之间存在关系。 (c)2005 Elsevier B.V.保留所有权利。

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