Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
J Neurochem. 2013 Jul;126(1):122-30. doi: 10.1111/jnc.12172. Epub 2013 Feb 27.
Spinal and bulbar muscular atrophy (SBMA) is an inherited motor neuron disease caused by the expansion of a polyglutamine (polyQ) tract within the androgen receptor (AR) gene. The pathologic features of SBMA are motor neuron loss in the spinal cord and brainstem, and diffuse nuclear accumulation and nuclear inclusions of mutant AR in residual motor neurons and certain visceral organs. AR-associated coregulator 70 (ARA70) was the first coregulator of AR to be identified, and it has been shown to interact with AR and increase its protein stability. Here, we report that genistein, an isoflavone found in soy, disrupts the interaction between AR and ARA70 and promotes the degradation of mutant AR in neuronal cells and transgenic mouse models of SBMA. We also demonstrate that dietary genistein ameliorates behavioral abnormalities, improves spinal cord and muscle pathology, and decreases the amounts of monomeric AR and high-molecular-weight mutant AR protein aggregates in SBMA transgenic mice. Thus, genistein treatment may be a potential therapeutic approach for alleviating the symptoms of SBMA by disrupting the interactions between AR and ARA70.
脊髓延髓肌肉萎缩症(SBMA)是一种遗传性运动神经元疾病,由雄激素受体(AR)基因内的多聚谷氨酰胺(polyQ)序列扩展引起。SBMA 的病理特征是脊髓和脑干运动神经元丧失,以及残留运动神经元和某些内脏器官中突变 AR 的弥散性核积聚和核内包涵体。AR 相关共激活因子 70(ARA70)是第一个被鉴定的 AR 共激活因子,它已被证明与 AR 相互作用并增加其蛋白稳定性。在这里,我们报告说,大豆中发现的异黄酮染料木黄酮会破坏 AR 和 ARA70 之间的相互作用,并促进神经元细胞和 SBMA 转基因小鼠模型中突变 AR 的降解。我们还证明,饮食中的染料木黄酮可改善行为异常,改善脊髓和肌肉病理学,并减少 SBMA 转基因小鼠中单体 AR 和高分子量突变 AR 蛋白聚集体的含量。因此,通过破坏 AR 和 ARA70 之间的相互作用,染料木黄酮治疗可能是缓解 SBMA 症状的一种潜在治疗方法。