Poburski Dörte, Boerner Josefine Barbara, Koenig Michel, Ristow Michael, Thierbach René
Institute of Nutrition, Friedrich Schiller University (FSU) Jena, Dornburgerstraße 24, Jena D-07743, Germany.
Laboratoire de Génétique de Maladies Rares EA7402, Institut Universitaire de Recherche Clinique, Université de Montpellier, Montpellier F-34093, France.
Biol Open. 2016 May 15;5(5):654-61. doi: 10.1242/bio.017004.
Friedreich ataxia is a neurodegenerative disease caused by a GAA triplet repeat expansion in the first intron of the frataxin gene, which results in reduced expression levels of the corresponding protein. Despite numerous animal and cellular models, therapeutic options that mechanistically address impaired frataxin expression are lacking. Here, we have developed a new mammalian cell model employing the Cre/loxP recombination system to induce a homozygous or heterozygous frataxin knockout in mouse embryonic fibroblasts. Induction of Cre-mediated disruption by tamoxifen was successfully tested on RNA and protein levels. After loss of frataxin protein, cell division, aconitase activity and oxygen consumption rates were found to be decreased, while ROS production was increased in the homozygous state. By contrast, in the heterozygous state no such changes were observed. A time-resolved analysis revealed the loss of aconitase activity as an initial event after induction of complete frataxin deficiency, followed by secondarily elevated ROS production and a late increase in iron content. Initial impairments of oxygen consumption and ATP production were found to be compensated in the late state and seemed to play a minor role in Friedreich ataxia pathophysiology. In conclusion and as predicted from its proposed role in iron sulfur cluster (ISC) biosynthesis, disruption of frataxin primarily causes impaired function of ISC-containing enzymes, whereas other consequences, including elevated ROS production and iron accumulation, appear secondary. These parameters and the robustness of the newly established system may additionally be used for a time-resolved study of pharmacological candidates in a HTS manner.
弗里德赖希共济失调是一种神经退行性疾病,由frataxin基因第一内含子中的GAA三联体重复扩增引起,导致相应蛋白质的表达水平降低。尽管有众多动物和细胞模型,但缺乏从机制上解决frataxin表达受损问题的治疗选择。在此,我们开发了一种新的哺乳动物细胞模型,采用Cre/loxP重组系统在小鼠胚胎成纤维细胞中诱导纯合或杂合的frataxin基因敲除。通过他莫昔芬诱导Cre介导的破坏在RNA和蛋白质水平上得到了成功验证。frataxin蛋白缺失后,发现细胞分裂、乌头酸酶活性和氧消耗率降低,而纯合状态下活性氧生成增加。相比之下,在杂合状态下未观察到此类变化。时间分辨分析显示,在诱导完全frataxin缺乏后,乌头酸酶活性丧失是初始事件,随后活性氧生成继发升高,铁含量后期增加。发现氧消耗和ATP生成的初始损伤在后期得到补偿,似乎在弗里德赖希共济失调病理生理学中起次要作用。总之,正如从其在铁硫簇(ISC)生物合成中的假定作用所预测的那样,frataxin的破坏主要导致含ISC酶的功能受损,而其他后果,包括活性氧生成增加和铁积累,似乎是次要的。这些参数以及新建立系统的稳健性还可用于以高通量筛选方式对候选药物进行时间分辨研究。