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融合肉瘤神经病理学与神经退行性疾病。

Fused in Sarcoma Neuropathology in Neurodegenerative Disease.

机构信息

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.

出版信息

Cold Spring Harb Perspect Med. 2017 Dec 1;7(12):a024299. doi: 10.1101/cshperspect.a024299.

Abstract

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.

摘要

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。

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Fused in Sarcoma Neuropathology in Neurodegenerative Disease.融合肉瘤神经病理学与神经退行性疾病。
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Annu Rev Biochem. 2015;84:355-79. doi: 10.1146/annurev-biochem-060614-034325. Epub 2014 Dec 8.
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The role of FUS gene variants in neurodegenerative diseases.FUS 基因突变在神经退行性疾病中的作用。
Nat Rev Neurol. 2014 Jun;10(6):337-48. doi: 10.1038/nrneurol.2014.78. Epub 2014 May 20.
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Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS.蛋白 N-精氨酸甲基转移酶的突变不是 FTLD-FUS 的病因。
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