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首页> 外文期刊>American Journal of Physiology >Contractile activity-induced adaptations in the mitochondrial protein import system.
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Contractile activity-induced adaptations in the mitochondrial protein import system.

机译:线粒体蛋白质输入系统中的收缩活动诱导的适应。

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We previously demonstrated that subsarcolemmal (SS) and intermyofibrillar (IMF) mitochondrial subfractions import proteins at different rates. This study was undertaken to investigate 1) whether protein import is altered by chronic contractile activity, which induces mitochondrial biogenesis, and 2) whether these two subfractions adapt similarly. Using electrical stimulation (10 Hz, 3 h/day for 7 and 14 days) to induce contractile activity, we observed that malate dehydrogenase import into the matrix of the SS and IMF mitochondia isolated from stimulated muscle was significantly increased by 1.4-to 1.7-fold, although the pattern of increase differed for each subfraction. This acceleration of import may be mitochondrial compartment specific, since the import of Bcl-2 into the outer membrane was not affected. Contractile activity also modified the mitochondrial content of proteins comprising the import machinery, as evident from increases in the levels of the intramitochondrial chaperone mtHSP70 as well as the outer membrane import receptor Tom20 in SS and IMF mitochondria. Addition of cytosol isolated from stimulated or control muscles to the import reaction resulted in similar twofold increases in the ability of mitochondria to import malate dehydrogenase, despite elevations in the concentration of mitochondrial import-stimulating factor within the cytosol of chronically stimulated muscle. These results suggest that chronic contractile activity modifies the extra- and intramitochondrial environments in a fashion that favors the acceleration of precursor protein import into the matrix of the organelle. This increase in protein import is likely an important adaptation in the overall process of mitochondrial biogenesis.
机译:我们以前证明了肌膜下(SS)和肌原纤维间(IMF)线粒体亚组分以不同的速率导入蛋白质。进行这项研究的目的是调查1)蛋白质的导入是否被诱导线粒体生物发生的慢性收缩活性所改变,以及2)这两个亚组分是否具有相似的适应性。使用电刺激(10 Hz,3小时/天,连续7天和14天)诱导收缩活动,我们观察到从刺激肌肉中分离出来的SS和IMF线粒体基质中苹果酸脱氢酶的导入量显着增加了1.4-至1.7-折,尽管每个子分数的增加方式都不同。这种导入的加速可能是特定于线粒体区室的,因为不影响Bcl-2导入外膜。收缩活性还改变了构成输入机制的蛋白质的线粒体含量,这从SS和IMF线粒体中线粒体内伴侣mtHSP70以及外膜输入受体Tom20的水平增加中就可以看出。从被刺激或控制的肌肉中分离出的细胞溶质添加到输入反应中,尽管线粒体输入刺激因子在慢性被刺激肌肉的细胞质中的浓度升高,但线粒体输入苹果酸脱氢酶的能力却增加了两倍。这些结果表明,慢性收缩活性以有利于前体蛋白导入细胞器基质中的加速方式改变了线粒体外和线粒体环境。蛋白质进口的增加可能是线粒体生物发生整个过程的重要适应。

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