Poort Jessica E, Rheuben Mary B, Breedlove S Marc, Jordan Cynthia L
Neuroscience Program, Michigan State University, MI, USA.
Neuroscience Program, Michigan State University, MI, USA
Hum Mol Genet. 2016 Sep 1;25(17):3768-3783. doi: 10.1093/hmg/ddw222. Epub 2016 Aug 4.
Spinal bulbar muscular atrophy (SBMA) is a progressive, late onset neuromuscular disease causing motor dysfunction in men. While the morphology of the neuromuscular junction (NMJ) is typically affected by neuromuscular disease, whether NMJs in SBMA are similarly affected by disease is not known. Such information will shed light on whether defective NMJs might contribute to the loss of motor function and represent a potential therapeutic target for treating symptoms of SBMA. To address this gap in information, the morphology of NMJs was examined in two mouse models of SBMA, a myogenic model that overexpresses wildtype androgen receptor (AR) exclusively in muscle fibres and a knockin (KI) model expressing a humanized mutant AR gene. The tripartite motor synapse consisting of motor nerve terminal, terminal Schwann cells (tSCs) and postsynaptic specialization were visualized and analysed using confocal microscopy. Counter to expectation, we found no evidence of denervation in either model, but junctions in both models show pathological fragmentation and an abnormal synaptophysin distribution consistent with functionally weak synapses. Neurofilament accumulations were observed only in the myogenic model, even though axonal transport dysfunction is characteristic of both models. The ultrastructure of NMJs revealed additional pathology, including deficits in docked vesicles presynaptically, wider synaptic clefts, and simpler secondary folds postsynaptically. The observed pathology of NMJs in diseased SBMA mice is likely the morphological correlates of defects in synaptic function which may underlie motor impairments associated with SBMA.
脊髓延髓性肌萎缩症(SBMA)是一种渐进性、迟发性神经肌肉疾病,会导致男性出现运动功能障碍。虽然神经肌肉接头(NMJ)的形态通常会受到神经肌肉疾病的影响,但SBMA中的神经肌肉接头是否同样受到疾病影响尚不清楚。这些信息将有助于了解有缺陷的神经肌肉接头是否可能导致运动功能丧失,并代表治疗SBMA症状的潜在治疗靶点。为了填补这一信息空白,我们在两种SBMA小鼠模型中检查了神经肌肉接头的形态,一种是仅在肌纤维中过表达野生型雄激素受体(AR)的肌源性模型,另一种是表达人源化突变AR基因的敲入(KI)模型。使用共聚焦显微镜对由运动神经末梢、终末雪旺细胞(tSCs)和突触后特化组成的三联运动突触进行可视化和分析。与预期相反,我们在两种模型中均未发现去神经支配的证据,但两种模型中的接头均显示出病理碎片化和异常的突触素分布,这与功能较弱的突触一致。仅在肌源性模型中观察到神经丝积聚,尽管轴突运输功能障碍是两种模型的特征。神经肌肉接头的超微结构显示出额外的病理学特征,包括突触前对接小泡的缺陷、更宽的突触间隙和突触后更简单的次级褶皱。在患病的SBMA小鼠中观察到的神经肌肉接头病理学可能是突触功能缺陷的形态学相关因素,这可能是与SBMA相关的运动障碍的基础。