Department of Neurology, University of Michigan Health System, Ann Arbor, 48109-2200, USA.
Acta Neuropathol. 2012 Nov;124(5):749-60. doi: 10.1007/s00401-012-1005-5. Epub 2012 Jun 27.
We report a retrospective case series of four patients with genetically confirmed Huntington's disease (HD) and sporadic amyotrophic lateral sclerosis (ALS), examining the brain and spinal cord in two cases. Neuropathological assessment included a polyglutamine recruitment method to detect sites of active polyglutamine aggregation, and biochemical and immunohistochemical assessment of TDP-43 pathology. The clinical sequence of HD and ALS varied, with the onset of ALS occurring after the mid-50's in all cases. Neuropathologic features of HD and ALS coexisted in both cases examined pathologically: neuronal loss and gliosis in the neostriatum and upper and lower motor neurons, with Bunina bodies and ubiquitin-immunoreactive skein-like inclusions in remaining lower motor neurons. One case showed relatively early HD pathology while the other was advanced. Expanded polyglutamine-immunoreactive inclusions and TDP-43-immunoreactive inclusions were widespread in many regions of the CNS, including the motor cortex and spinal anterior horn. Although these two different proteinaceous inclusions coexisted in a small number of neurons, the two proteins did not co-localize within inclusions. The regional distribution of TDP-43-immunoreactive inclusions in the cerebral cortex partly overlapped with that of expanded polyglutamine-immunoreactive inclusions. In the one case examined by TDP-43 immunoblotting, similar TDP-43 isoforms were observed as in ALS. Our findings suggest the possibility that a rare subset of older HD patients is prone to develop features of ALS with an atypical TDP-43 distribution that resembles that of aggregated mutant huntingtin. Age-dependent neuronal dysfunction induced by mutant polyglutamine protein expression may contribute to later-life development of TDP-43 associated motor neuron disease in a small subset of patients with HD.
我们报告了四例遗传性亨廷顿病(HD)和散发性肌萎缩侧索硬化症(ALS)患者的回顾性病例系列,对其中两例进行了大脑和脊髓检查。神经病理学评估包括一种聚谷氨酰胺募集方法,以检测活性聚谷氨酰胺聚集的部位,以及 TDP-43 病理学的生化和免疫组织化学评估。HD 和 ALS 的临床序列不同,所有病例的 ALS 发病均在 50 多岁以后。在检查的两例中,HD 和 ALS 的神经病理学特征共存:新纹状体和上下运动神经元的神经元丢失和神经胶质增生,伴有 Bunina 体和剩余下运动神经元中泛素免疫反应性线样包涵体。一例表现为相对早期的 HD 病理学,另一例则较为晚期。扩展的聚谷氨酰胺免疫反应性包涵体和 TDP-43 免疫反应性包涵体广泛存在于中枢神经系统的许多区域,包括运动皮层和脊髓前角。尽管这两种不同的蛋白包涵体共存于少数神经元中,但这两种蛋白并未在包涵体中共同定位。大脑皮层中 TDP-43 免疫反应性包涵体的区域分布与扩展的聚谷氨酰胺免疫反应性包涵体部分重叠。在通过 TDP-43 免疫印迹检查的一例中,观察到与 ALS 相似的 TDP-43 同工型。我们的发现表明,少数较年长的 HD 患者可能具有 ALS 的特征,其 TDP-43 分布不典型,类似于聚集的突变 huntingtin。突变聚谷氨酰胺蛋白表达引起的年龄依赖性神经元功能障碍可能导致一小部分 HD 患者发生 TDP-43 相关运动神经元疾病。