Holm Ida E, Alstrup Aage Kristian Olsen, Luo Yonglun
Department of Pathology, Randers Hospital, 8930, Randers, Denmark.
Department of Clinical Medicine, Aarhus University, 8000, Aarhus C, Denmark.
J Pathol. 2016 Jan;238(2):267-87. doi: 10.1002/path.4654. Epub 2015 Nov 28.
Increasing incidence of neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease has become one of the most challenging health issues in ageing humans. One approach to combat this is to generate genetically modified animal models of neurodegenerative disorders for studying pathogenesis, prognosis, diagnosis, treatment, and prevention. Owing to the genetic, anatomic, physiologic, pathologic, and neurologic similarities between pigs and humans, genetically modified pig models of neurodegenerative disorders have been attractive large animal models to bridge the gap of preclinical investigations between rodents and humans. In this review, we provide a neuroanatomical overview in pigs and summarize and discuss the generation of genetically modified pig models of neurodegenerative disorders including Alzheimer's diseases, Huntington's disease, Parkinson's disease, amyotrophic lateral sclerosis, spinal muscular atrophy, and ataxia-telangiectasia. We also highlight how non-invasive bioimaging technologies such as positron emission tomography (PET), computer tomography (CT), and magnetic resonance imaging (MRI), and behavioural testing have been applied to characterize neurodegenerative pig models. We further propose a multiplex genome editing and preterm recloning (MAP) approach by using the rapid growth of the ground-breaking precision genome editing technology CRISPR/Cas9 and somatic cell nuclear transfer (SCNT). With this approach, we hope to shorten the temporal requirement in generating multiple transgenic pigs, increase the survival rate of founder pigs, and generate genetically modified pigs that will more closely resemble the disease-causing mutations and recapitulate pathological features of human conditions.
阿尔茨海默病和帕金森病等神经退行性疾病发病率的不断上升,已成为老龄化人群面临的最具挑战性的健康问题之一。应对这一问题的一种方法是构建神经退行性疾病的转基因动物模型,用于研究发病机制、预后、诊断、治疗和预防。由于猪与人类在基因、解剖、生理、病理和神经方面存在相似性,神经退行性疾病的转基因猪模型已成为有吸引力的大型动物模型,以弥合啮齿动物和人类之间临床前研究的差距。在这篇综述中,我们提供了猪的神经解剖学概述,并总结和讨论了神经退行性疾病转基因猪模型的构建,包括阿尔茨海默病、亨廷顿病、帕金森病、肌萎缩侧索硬化症、脊髓性肌萎缩症和共济失调毛细血管扩张症。我们还强调了正电子发射断层扫描(PET)、计算机断层扫描(CT)和磁共振成像(MRI)等非侵入性生物成像技术以及行为测试如何被应用于表征神经退行性猪模型。我们进一步提出了一种多重基因组编辑和早产再克隆(MAP)方法,利用开创性的精确基因组编辑技术CRISPR/Cas9的快速发展和体细胞核移植(SCNT)。通过这种方法,我们希望缩短生成多只转基因猪的时间要求,提高代孕猪的存活率,并生成更接近致病突变并概括人类疾病病理特征的转基因猪。