Liang Chun-Chi, Tanabe Lauren M, Jou Stephanie, Chi Frank, Dauer William T
J Clin Invest. 2014 Jul;124(7):3080-92. doi: 10.1172/JCI72830. Epub 2014 Jun 17.
Lack of a preclinical model of primary dystonia that exhibits dystonic-like twisting movements has stymied identification of the cellular and molecular underpinnings of the disease. The classical familial form of primary dystonia is caused by the DYT1 (ΔE) mutation in TOR1A, which encodes torsinA, AAA⁺ ATPase resident in the lumen of the endoplasmic reticular/nuclear envelope. Here, we found that conditional deletion of Tor1a in the CNS (nestin-Cre Tor1a(flox/-)) or isolated CNS expression of DYT1 mutant torsinA (nestin-Cre Tor1a(flox/ΔE)) causes striking abnormal twisting movements. These animals developed perinuclear accumulation of ubiquitin and the E3 ubiquitin ligase HRD1 in discrete sensorimotor regions, followed by neurodegeneration that was substantially milder in nestin-Cre Tor1a(flox/ΔE) compared with nestin-Cre Tor1a(flox/-) animals. Similar to the neurodevelopmental onset of DYT1 dystonia in humans, the behavioral and histopathological abnormalities emerged and became fixed during CNS maturation in the murine models. Our results establish a genetic model of primary dystonia that is overtly symptomatic, and link torsinA hypofunction to neurodegeneration and abnormal twisting movements. These findings provide a cellular and molecular framework for how impaired torsinA function selectively disrupts neural circuits and raise the possibility that discrete foci of neurodegeneration may contribute to the pathogenesis of DYT1 dystonia.
缺乏能够表现出肌张力障碍样扭转运动的原发性肌张力障碍临床前模型,阻碍了对该疾病细胞和分子基础的识别。原发性肌张力障碍的经典家族形式是由TOR1A中的DYT1(ΔE)突变引起的,TOR1A编码torsinA,一种位于内质网/核膜腔中的AAA⁺ATP酶。在这里,我们发现,在中枢神经系统中条件性缺失Tor1a(nestin-Cre Tor1a(flox/-))或孤立地在中枢神经系统中表达DYT1突变型torsinA(nestin-Cre Tor1a(flox/ΔE))会导致明显的异常扭转运动。这些动物在离散的感觉运动区域出现泛素和E3泛素连接酶HRD1的核周积聚,随后发生神经退行性变,与nestin-Cre Tor1a(flox/-)动物相比,nestin-Cre Tor1a(flox/ΔE)动物的神经退行性变明显较轻。与人类DYT1肌张力障碍的神经发育性发病相似,行为和组织病理学异常在小鼠模型的中枢神经系统成熟过程中出现并固定下来。我们的结果建立了一个具有明显症状的原发性肌张力障碍遗传模型,并将torsinA功能减退与神经退行性变和异常扭转运动联系起来。这些发现为torsinA功能受损如何选择性破坏神经回路提供了一个细胞和分子框架,并增加了神经退行性变的离散病灶可能导致DYT1肌张力障碍发病机制的可能性。