Department Of Clinical Neuropathology, Academic Neuroscience Building, King's College Hospital, Denmark Hill, SE5 9RS, London, UK.
MRC London Neurodegenerative Diseases Brain Bank, Institute of Psychiatry, Psychology and Neuroscience, King's College London, SE5 8AF, London, UK.
Acta Neuropathol Commun. 2015 Oct 9;3:62. doi: 10.1186/s40478-015-0235-x.
Mutations in the FUS gene have been shown to be a rare cause of amyotrophic lateral sclerosis (ALS-FUS) and whilst well documented clinically and genetically there have been relatively few neuropathological studies.Recent work suggested a possible correlation between pathological features such as frequency of basophilic inclusions in neurons and rate of clinical decline, other studies have revealed a discrepancy between the upper motor neuron features detected clinically and the associated pathology. The purpose of this study was to describe the pathological features associated with more recently discovered FUS mutations and reinvestigate those with well recognised mutations in an attempt to correlate the pathology with mutation and/or clinical phenotype. The brains and spinal cords of seven cases of ALS-FUS were examined neuropathologically, including cases with the newly described p.K510E mutation and a case with both a known p.P525L mutation in the FUS gene and a truncating p.Y374X mutation in the TARDBP gene.
The neuropathology in all cases revealed basophilic and FUS inclusions in the cord. The density and type of inclusions varied markedly between cases, but did not allow a clear correlation with clinical progression. Only one case showed significant motor cortical pathology despite the upper motor neuron clinical features being evident in 4 patients. The case with both a FUS and TARDBP mutation revealed FUS positive inclusions but no TDP-43 pathology. Instead there were unusual p62 positive, FUS negative neuronal and glial inclusions as well as dot-like neurites.
The study confirms cases of ALS-FUS to be mainly a lower motor neuron disease and to have pathology that does not appear to neatly correlate with clinical features or genetics. Furthermore, the case with both a FUS and TARDBP mutation reveals an intriguing pathological profile which at least in part involves a very unusual staining pattern for the ubiquitin-binding protein p62.
FUS 基因突变已被证实是肌萎缩侧索硬化症(ALS-FUS)的罕见病因。尽管临床和遗传学方面已有充分记录,但神经病理学研究相对较少。最近的研究表明,神经元中的嗜碱性包涵体的频率与临床下降速度之间可能存在相关性,其他研究则揭示了临床上检测到的上运动神经元特征与相关病理学之间的差异。本研究旨在描述与最近发现的 FUS 突变相关的病理特征,并重新研究那些具有公认突变的病例,试图将病理学与突变和/或临床表型相关联。对 7 例 ALS-FUS 患者的大脑和脊髓进行了神经病理学检查,包括新描述的 p.K510E 突变病例和 FUS 基因中已知的 p.P525L 突变病例以及 TARDBP 基因中截断的 p.Y374X 突变病例。
所有病例的神经病理学均显示脊髓中有嗜碱性和 FUS 包涵体。包涵体的密度和类型在病例之间差异很大,但无法与临床进展进行明确关联。尽管 4 例患者均有明显的上运动神经元临床特征,但仅有 1 例患者显示出显著的皮质运动病理学。同时存在 FUS 和 TARDBP 突变的病例显示 FUS 阳性包涵体,但无 TDP-43 病理学。相反,存在不寻常的 p62 阳性、FUS 阴性神经元和神经胶质包涵体以及点状神经突。
本研究证实 ALS-FUS 主要为下运动神经元疾病,且其病理学似乎与临床特征或遗传学没有明显关联。此外,同时存在 FUS 和 TARDBP 突变的病例揭示了一种引人入胜的病理谱,至少部分涉及到非常不寻常的泛素结合蛋白 p62 的染色模式。