Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia V6T 2B5, Canada.
Department of Neuropathology, University of Tübingen and German Center for Neurodegenerative Diseases (DZNE), Tübingen 72076, Germany.
Cold Spring Harb Perspect Med. 2017 Dec 1;7(12):a024299. doi: 10.1101/cshperspect.a024299.
Abnormal intracellular accumulation of the fused in sarcoma (FUS) protein is the characteristic pathological feature of cases of familial amyotrophic lateral sclerosis (ALS) caused by mutations (ALS-) and several uncommon disorders that may present with sporadic frontotemporal dementia (FTLD-FUS). Although these findings provide further support for the concept that ALS and FTD are closely related clinical syndromes with an overlapping molecular basis, important differences in the pathological features and results from experimental models indicate that ALS- and FTLD-FUS have distinct pathogenic mechanisms.
融合于肉瘤(FUS)蛋白的异常细胞内积累是由 突变(ALS-)引起的家族性肌萎缩侧索硬化症(ALS)病例和几种可能表现为散发性额颞叶痴呆(FTLD-FUS)的罕见疾病的特征性病理特征。尽管这些发现进一步支持了 ALS 和 FTD 是具有重叠分子基础的密切相关的临床综合征的概念,但实验模型中的病理特征和结果的重要差异表明 ALS-和 FTLD-FUS 具有不同的发病机制。