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体外衍生的人类神经元在神经退行性疾病建模中的应用。

The application of in vitro-derived human neurons in neurodegenerative disease modeling.

机构信息

Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.

Department of Pathology, University of Washington, Seattle, WA, USA.

出版信息

J Neurosci Res. 2021 Jan;99(1):124-140. doi: 10.1002/jnr.24615. Epub 2020 Mar 13.

Abstract

The development of safe and effective treatments for age-associated neurodegenerative disorders is an on-going challenge faced by the scientific field. Key to the development of such therapies is the appropriate selection of modeling systems in which to investigate disease mechanisms and to test candidate interventions. There are unique challenges in the development of representative laboratory models of neurodegenerative diseases, including the complexity of the human brain, the cumulative and variable contributions of genetic and environmental factors over the course of a lifetime, inability to culture human primary neurons, and critical central nervous system differences between small animal models and humans. While traditional rodent models have advanced our understanding of neurodegenerative disease mechanisms, key divergences such as the species-specific genetic background can limit the application of animal models in many cases. Here we review in vitro human neuronal systems that employ stem cell and reprogramming technology and their application to a range of neurodegenerative diseases. Specifically, we compare human-induced pluripotent stem cell-derived neurons to directly converted, or transdifferentiated, induced neurons, as both model systems can take advantage of patient-derived human tissue to produce neurons in culture. We present recent technical developments using these two modeling systems, as well as current limitations to these systems, with the aim of advancing investigation of neuropathogenic mechanisms using these models.

摘要

开发针对与年龄相关的神经退行性疾病的安全有效的治疗方法是科学界面临的持续挑战。此类疗法的开发关键是适当选择建模系统,以研究疾病机制并测试候选干预措施。开发神经退行性疾病的代表性实验室模型存在独特的挑战,包括人脑的复杂性、遗传和环境因素在一生中的累积和可变贡献、无法培养人类原代神经元以及小动物模型和人类之间的关键中枢神经系统差异。虽然传统的啮齿动物模型推进了我们对神经退行性疾病机制的理解,但特定物种的遗传背景等关键差异在许多情况下限制了动物模型的应用。在这里,我们回顾了利用干细胞和重编程技术的体外人类神经元系统及其在一系列神经退行性疾病中的应用。具体来说,我们将源自人类诱导多能干细胞的神经元与直接转化或转分化的诱导神经元进行比较,因为这两种模型系统都可以利用患者来源的人类组织在培养中产生神经元。我们介绍了这两种建模系统的最新技术进展,以及这些系统目前的局限性,旨在通过这些模型推进对神经发病机制的研究。

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