Polinski Nicole K, Puoliväli Jukka, Rauhala Leena, Stenius Taina-Kaisa, Bragge Timo, Parkkari Teija, Penttinen Anna-Maija, Chen Yi, Mabrouk Omar S, Glajch Kelly E, Hirst Warren D, Perkinton Michael, Martinez Terina N, Frasier Mark A
Research Programs, The Michael J. Fox Foundation for Parkinson's Research, New York, New York, United States of America.
Charles River Discovery Research Services, Charles River Laboratories, Kuopio, Finland.
PLoS One. 2025 Aug 8;20(8):e0329823. doi: 10.1371/journal.pone.0329823. eCollection 2025.
Alpha-synuclein (aSyn) is linked to Parkinson's disease (PD) through SNCA genetic mutations, phosphorylated aSyn in Lewy bodies and Lewy neurites, and most recently through evidence of aSyn aggregation in patient spinal fluid using the aSyn seed amplification assay. Therefore, understanding the biology of this protein and developing therapeutic interventions targeting pathological processing of aSyn are a key area of focus for novel treatments to slow or stop PD. Reliable preclinical models are imperative for these efforts. To this end, we developed a novel model using CRISPR/Cas9 to humanize the regions surrounding the naturally occurring threonine 53 amino acid in the Sprague Dawley rat to generate a humanized A53T aSyn rat model (aSyn A53T KI). We also generated an Snca knockout (aSyn KO) line to pair with the humanized A53T aSyn rat line to confirm that phenotypes were not due to loss of endogenous rat aSyn protein. A systematic phenotyping study was performed on these lines, assessing PD-related pathology and phenotypes at multiple timepoints. The aSyn KO rat line was profiled at 6 and 12 months of age, revealing successful aSyn protein knockout. The aSyn A53T KI model was profiled at 4, 8, 12, and 18 months of age for motor and non-motor phenotypes, nigrostriatal degeneration, and brain pathology. We confirmed the aSyn A53T KI rat expresses human aSyn while lacking endogenous rat aSyn. Motor function and non-motor function remain largely unaffected in this model, and no overt nigrostriatal degeneration or brain pathology are observed up to 18 months of age. Although the aSyn A53T KI rat lacks the ability to model PD pathology and phenotypes at baseline, it is an ideal model for investigating the impact of exogenous synuclein aggregates or environmental triggers on human aSyn in an in vivo model system.
α-突触核蛋白(aSyn)通过SNCA基因突变、路易小体和路易神经突中的磷酸化aSyn,以及最近通过使用aSyn种子扩增试验在患者脑脊液中发现aSyn聚集的证据,与帕金森病(PD)相关联。因此,了解这种蛋白质的生物学特性并开发针对aSyn病理处理的治疗干预措施,是减缓或阻止PD的新型治疗方法的关键关注领域。可靠的临床前模型对于这些努力至关重要。为此,我们开发了一种新型模型,使用CRISPR/Cas9技术将斯普拉格-道利大鼠中天然存在的苏氨酸53氨基酸周围的区域人源化,以生成人源化A53T aSyn大鼠模型(aSyn A53T KI)。我们还生成了一个Snca基因敲除(aSyn KO)品系,与该人源化A53T aSyn大鼠品系配对,以确认表型不是由于内源性大鼠aSyn蛋白的缺失所致。对这些品系进行了系统的表型研究,在多个时间点评估与PD相关的病理学和表型。对aSyn KO大鼠品系在6个月和12个月龄时进行了分析,结果显示成功敲除了aSyn蛋白。对aSyn A53T KI模型在4个月、8个月、12个月和18个月龄时进行了运动和非运动表型、黑质纹状体变性及脑病理学分析。我们证实aSyn A53T KI大鼠表达人aSyn,同时缺乏内源性大鼠aSyn。在该模型中,运动功能和非运动功能在很大程度上未受影响,直至18个月龄均未观察到明显的黑质纹状体变性或脑病理学改变。尽管aSyn A53T KI大鼠在基线时缺乏模拟PD病理学和表型的能力,但它是在体内模型系统中研究外源性突触核蛋白聚集体或环境触发因素对人aSyn影响的理想模型。