Dulbecco Telethon Institute, Centre for Integrative Biology (CIBIO), University of Trento, 38123 Trento, Italy.
Department of Biomedical Sciences (DBS), University of Padova, 35131 Padova, Italy.
Cells. 2020 Jan 30;9(2):325. doi: 10.3390/cells9020325.
Polyglutamine (polyQ) expansions in the androgen receptor (AR) gene cause spinal and bulbar muscular atrophy (SBMA), a neuromuscular disease characterized by lower motor neuron (MN) loss and skeletal muscle atrophy, with an unknown mechanism. We generated new mouse models of SBMA for constitutive and inducible expression of mutant AR and performed biochemical, histological and functional analyses of phenotype. We show that polyQ-expanded AR causes motor dysfunction, premature death, IIb-to-IIa/IIx fiber-type change, glycolytic-to-oxidative fiber-type switching, upregulation of atrogenes and autophagy genes and mitochondrial dysfunction in skeletal muscle, together with signs of muscle denervation at late stage of disease. PolyQ expansions in the AR resulted in nuclear enrichment. Within the nucleus, mutant AR formed 2% sodium dodecyl sulfate (SDS)-resistant aggregates and inclusion bodies in myofibers, but not spinal cord and brainstem, in a process exacerbated by age and sex. Finally, we found that two-week induction of expression of polyQ-expanded AR in adult mice was sufficient to cause premature death, body weight loss and muscle atrophy, but not aggregation, metabolic alterations, motor coordination and fiber-type switch, indicating that expression of the disease protein in the adulthood is sufficient to recapitulate several, but not all SBMA manifestations in mice. These results imply that chronic expression of polyQ-expanded AR, i.e. during development and prepuberty, is key to induce the full SBMA muscle pathology observed in patients. Our data support a model whereby chronic expression of polyQ-expanded AR triggers muscle atrophy through toxic (neomorphic) gain of function mechanisms distinct from normal (hypermorphic) gain of function mechanisms.
多聚谷氨酰胺(polyQ)扩展在雄激素受体(AR)基因中导致脊髓和延髓肌肉萎缩症(SBMA),这是一种以运动神经元(MN)丧失和骨骼肌萎缩为特征的神经肌肉疾病,但机制尚不清楚。我们生成了新的 SBMA 小鼠模型,用于突变型 AR 的组成型和诱导性表达,并对表型进行了生化、组织学和功能分析。我们表明,polyQ 扩展的 AR 导致运动功能障碍、过早死亡、IIb 到 IIa/IIx 纤维类型变化、糖酵解到氧化纤维类型转换、肌肉萎缩症中自噬基因和自噬基因的上调以及线粒体功能障碍,以及疾病后期的肌肉失神经支配迹象。AR 中的 polyQ 扩展导致核富集。在核内,突变型 AR 在肌纤维中形成 2%十二烷基硫酸钠(SDS)抗性聚集体和包含体,但在脊髓和脑干中没有,这一过程随着年龄和性别而加剧。最后,我们发现,在成年小鼠中诱导表达 polyQ 扩展的 AR 两周足以导致过早死亡、体重减轻和肌肉萎缩,但不会引起聚集、代谢改变、运动协调和纤维类型转换,表明疾病蛋白在成年期的表达足以在小鼠中重现 SBMA 的几种,但不是所有表现。这些结果表明,polyQ 扩展的 AR 的慢性表达,即在发育和青春期前,是引发患者中观察到的完整 SBMA 肌肉病理学的关键。我们的数据支持这样一种模型,即 polyQ 扩展的 AR 的慢性表达通过与正常(超功能)获得性功能机制不同的毒性(新功能)获得性功能机制引发肌肉萎缩。