McComish Sarah F, MacMahon Copas Adina N, Caldwell Maeve A
Department of Physiology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Front Neurosci. 2022 May 16;16:851058. doi: 10.3389/fnins.2022.851058. eCollection 2022.
Parkinson's disease (PD) is the second most common neurodegenerative disease and affects approximately 2-3% of the population over the age of 65. PD is characterised by the loss of dopaminergic neurons from the substantia nigra, leading to debilitating motor symptoms including bradykinesia, tremor, rigidity, and postural instability. PD also results in a host of non-motor symptoms such as cognitive decline, sleep disturbances and depression. Although existing therapies can successfully manage some motor symptoms for several years, there is still no means to halt progression of this severely debilitating disorder. Animal models used to replicate aspects of PD have contributed greatly to our current understanding but do not fully replicate pathological mechanisms as they occur in patients. Because of this, there is now great interest in the use of human brain-based models to help further our understanding of disease processes. Human brain-based models include those derived from embryonic stem cells, patient-derived induced neurons, induced pluripotent stem cells and brain organoids, as well as post-mortem tissue. These models facilitate analysis of disease mechanisms and it is hoped they will help bridge the existing gap between bench and bedside. This review will discuss the various human brain-based models utilised in PD research today and highlight some of the key breakthroughs they have facilitated. Furthermore, the potential caveats associated with the use of human brain-based models will be detailed.
帕金森病(PD)是第二常见的神经退行性疾病,影响约2%-3%的65岁以上人群。帕金森病的特征是黑质中多巴胺能神经元的丧失,导致运动症状恶化,包括运动迟缓、震颤、僵硬和姿势不稳。帕金森病还会导致一系列非运动症状,如认知能力下降、睡眠障碍和抑郁症。尽管现有疗法可以成功控制一些运动症状数年,但仍然没有办法阻止这种严重致残疾病的进展。用于复制帕金森病某些方面的动物模型对我们目前的理解有很大贡献,但不能完全复制患者体内发生的病理机制。因此,目前人们对使用基于人脑的模型来帮助进一步了解疾病过程非常感兴趣。基于人脑的模型包括那些源自胚胎干细胞、患者来源的诱导神经元、诱导多能干细胞和脑类器官以及死后组织的模型。这些模型有助于分析疾病机制,人们希望它们将有助于弥合目前基础研究与临床应用之间的差距。本综述将讨论当今帕金森病研究中使用的各种基于人脑的模型,并强调它们所促成的一些关键突破。此外,还将详细介绍使用基于人脑的模型可能存在的问题。