Department of Basic Medical Sciences, Neurosciences and Sensory Organs, Medical School, University of Bari, Piazza Giulio Cesare, 11. I-70124 Bari, Italy.
Molecules. 2020 Sep 7;25(18):4085. doi: 10.3390/molecules25184085.
In this study, the neural phenotype is explored in rodent models of the spinocerebellar disorder known as the Friedreich Ataxia (FA), which results from mutations within the gene encoding the Frataxin mitochondrial protein. For this, the M12 line, bearing a targeted mutation, which disrupts the Frataxin gene exon 4 was used, together with the M02 line, which, in addition, is hemizygous for the human Frataxin gene mutation (Pook transgene), implying the occurrence of 82-190 GAA repeats within its first intron. The mutant mice phenotype was compared to the one of wild type littermates in regions undergoing differential profiles of neurogenesis, including the cerebellar cortex and the spinal cord by using neuronal (β-tubulin) and glial (Glial Fibrillary Acidic Protein) markers as well as the Contactin 1 axonal glycoprotein, involved in neurite growth control. Morphological/morphometric analyses revealed that while in Frataxin mutant mice the neuronal phenotype was significantly counteracted, a glial upregulation occurred at the same time. Furthermore, Contactin 1 downregulation suggested that changes in the underlying gene contributed to the disorder pathogenesis. Therefore, the FA phenotype implies an alteration of the developmental profile of neuronal and glial precursors. Finally, epigallocatechin gallate polyphenol administration counteracted the disorder, indicating protective effects of antioxidant administration.
在这项研究中,探索了已知的脊髓小脑失调疾病(即弗里德里希共济失调症,FA)的啮齿动物模型中的神经表型,这种疾病是由编码线粒体蛋白 Frataxin 的基因突变引起的。为此,使用了携带靶向突变的 M12 系,该突变破坏了 Frataxin 基因外显子 4,以及 M02 系,该系除了携带人类 Frataxin 基因突变(Pook 转基因)的半合子之外,其第一个内含子中还存在 82-190 GAA 重复。通过使用神经元(β-微管蛋白)和神经胶质(神经胶质酸性蛋白)标志物以及参与神经突生长控制的 Contactin 1 轴突糖蛋白,比较了突变小鼠与野生型同窝仔鼠在经历神经发生差异图谱的区域中的表型,包括小脑皮层和脊髓。形态学/形态计量学分析表明,尽管在 Frataxin 突变小鼠中神经元表型显著受到抑制,但同时也发生了神经胶质的上调。此外,Contactin 1 的下调表明,潜在基因的变化导致了疾病的发病机制。因此,FA 表型意味着神经元和神经胶质前体细胞的发育谱发生了改变。最后,表没食子儿茶素没食子酸酯多酚的给药可逆转该疾病,表明抗氧化剂给药具有保护作用。