Dauth Stephanie, Maoz Ben M, Sheehy Sean P, Hemphill Matthew A, Murty Tara, Macedonia Mary Kate, Greer Angie M, Budnik Bogdan, Parker Kevin Kit
Disease Biophysics Group, Wyss Institute for Biologically Inspired Engineering, John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts; and.
Mass Spectrometry and Proteomics Resource Laboratory, Harvard University, Cambridge, Massachusetts.
J Neurophysiol. 2017 Mar 1;117(3):1320-1341. doi: 10.1152/jn.00575.2016. Epub 2016 Dec 28.
Brain in vitro models are critically important to developing our understanding of basic nervous system cellular physiology, potential neurotoxic effects of chemicals, and specific cellular mechanisms of many disease states. In this study, we sought to address key shortcomings of current brain in vitro models: the scarcity of comparative data for cells originating from distinct brain regions and the lack of multiregional brain in vitro models. We demonstrated that rat neurons from different brain regions exhibit unique profiles regarding their cell composition, protein expression, metabolism, and electrical activity in vitro. In vivo, the brain is unique in its structural and functional organization, and the interactions and communication between different brain areas are essential components of proper brain function. This fact and the observation that neurons from different areas of the brain exhibit unique behaviors in vitro underline the importance of establishing multiregional brain in vitro models. Therefore, we here developed a multiregional brain-on-a-chip and observed a reduction of overall firing activity, as well as altered amounts of astrocytes and specific neuronal cell types compared with separately cultured neurons. Furthermore, this multiregional model was used to study the effects of phencyclidine, a drug known to induce schizophrenia-like symptoms in vivo, on individual brain areas separately while monitoring downstream effects on interconnected regions. Overall, this work provides a comparison of cells from different brain regions in vitro and introduces a multiregional brain-on-a-chip that enables the development of unique disease models incorporating essential in vivo features. Due to the scarcity of comparative data for cells from different brain regions in vitro, we demonstrated that neurons isolated from distinct brain areas exhibit unique behaviors in vitro. Moreover, in vivo proper brain function is dependent on the connection and communication of several brain regions, underlining the importance of developing multiregional brain in vitro models. We introduced a novel brain-on-a-chip model, implementing essential in vivo features, such as different brain areas and their functional connections.
脑体外模型对于深化我们对基础神经系统细胞生理学、化学物质潜在神经毒性作用以及许多疾病状态的特定细胞机制的理解至关重要。在本研究中,我们试图解决当前脑体外模型的关键缺陷:源自不同脑区的细胞缺乏比较数据,以及缺乏多区域脑体外模型。我们证明,来自不同脑区的大鼠神经元在体外的细胞组成、蛋白质表达、代谢和电活动方面表现出独特的特征。在体内,大脑在其结构和功能组织方面独具特色,不同脑区之间的相互作用和交流是正常脑功能的重要组成部分。这一事实以及不同脑区的神经元在体外表现出独特行为的观察结果强调了建立多区域脑体外模型的重要性。因此,我们在此开发了一种多区域芯片脑模型,并观察到与单独培养的神经元相比,整体放电活动减少,星形胶质细胞和特定神经元细胞类型的数量也发生了变化。此外,该多区域模型用于研究苯环利定(一种已知在体内可诱发精神分裂症样症状的药物)对各个脑区的影响,同时监测对相互连接区域的下游效应。总体而言,这项工作提供了不同脑区细胞在体外的比较,并引入了一种多区域芯片脑模型,该模型能够开发包含重要体内特征的独特疾病模型。由于体外不同脑区细胞的比较数据稀缺,我们证明从不同脑区分离的神经元在体外表现出独特行为。此外,体内正常脑功能依赖于多个脑区的连接和交流,这强调了开发多区域脑体外模型的重要性。我们引入了一种新型芯片脑模型,实现了不同脑区及其功能连接等重要体内特征。