Department of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.
Acta Neuropathol Commun. 2018 Jul 20;6(1):63. doi: 10.1186/s40478-018-0564-7.
Frontotemporal lobar degeneration (FTLD) is heterogeneous in clinical presentation, neuropathological characteristics and genetics. An expanded GGGGCC hexanucleotide repeat in C9ORF72 is the most common genetic cause of both FTLD and motor neuron disease (MND). Dipeptide repeat polymers (DPR) are generated through repeat-associated non-ATG translation, and they aggregate in neuronal inclusions with a distribution distinct from that of TDP-43 pathology. Recent studies from animal and cell culture models suggest that DPR might be toxic, but that toxicity may differ for specific DPR. Arginine containing DPR (poly-GR and poly-PR) have the greatest toxicity and are less frequent than other DPR (poly-GP, poly-GA). A unique feature of arginine-containing DPR is their potential for post-translational modification by methyl-transferases, which produces methylarginine DPR. In this report, we explored the relationship of DPR and methylarginine to markers of neurodegeneration using quantitative digital microscopic methods in 40 patients with C9ORF72 mutations and one of three different clinicopathologic phenotypes, FTLD, FTLD-MND or MND. We find that density and distribution of poly-GR inclusions are different from poly-GA and poly-GP inclusions. We also demonstrate colocalization of poly-GR with asymmetrical dimethylarginine (aDMA) immunoreactivity in regions with neurodegeneration. Differences in aDMA were also noted by clinical phenotype. FTLD-MND had the highest burden of poly-GR pathology compared to FTLD and MND, while FTLD-MND had higher burden of aDMA than FTLD. The results suggest that poly-GR pathology is associated with toxicity and neurodegeneration. It remains to be determined if dimethylarginine modification of poly-GR could contribute to its toxicity.
额颞叶变性(FTLD)在临床表现、神经病理学特征和遗传学上具有异质性。C9ORF72 中 GGGGCC 六核苷酸重复扩增是 FTLD 和运动神经元病(MND)的最常见遗传原因。二肽重复聚合物(DPR)是通过重复相关的非 ATG 翻译产生的,它们与 TDP-43 病理学的分布不同,在神经元包含体中聚集。来自动物和细胞培养模型的最近研究表明,DPR 可能具有毒性,但特定 DPR 的毒性可能不同。含精氨酸的 DPR(聚-GR 和聚-PR)毒性最大,且比其他 DPR(聚-GP、聚-GA)频率更低。含精氨酸的 DPR 的一个独特特征是它们可能通过甲基转移酶发生翻译后修饰,产生甲基精氨酸 DPR。在本报告中,我们使用定量数字显微镜方法,在 40 名 C9ORF72 突变患者和三种不同临床病理表型(FTLD、FTLD-MND 或 MND)中的一个患者中,研究了 DPR 和甲基精氨酸与神经退行性变标志物的关系。我们发现聚-GR 包含物的密度和分布与聚-GA 和聚-GP 包含物不同。我们还证明了聚-GR 与神经退行性变区域不对称二甲基精氨酸(aDMA)免疫反应性的共定位。临床表型也存在 aDMA 的差异。FTLD-MND 与 FTLD 和 MND 相比,聚-GR 病理学负担最高,而 FTLD-MND 的 aDMA 负担高于 FTLD。结果表明聚-GR 病理学与毒性和神经退行性变有关。精氨酸修饰的聚-GR 是否会导致其毒性仍有待确定。