Byun Youkyeong Gloria, Chung Won-Suk
Department of Biological Sciences, Korea Advanced Institute of Science and Technology.
Department of Biological Sciences, Korea Advanced Institute of Science and Technology;
J Vis Exp. 2018 Feb 5(132):56647. doi: 10.3791/56647.
Astrocytes are the major cell type in the brain and directly contact synapses and blood vessels. Although microglial cells have been considered the major immune cells and only phagocytes in the brain, recent studies have shown that astrocytes also participate in various phagocytic processes, such as developmental synapse elimination and clearance of amyloid beta plaques in Alzheimer's disease (AD). Despite these findings, the efficiency of astrocyte engulfment and degradation of their targets is unclear compared with that of microglia. This lack of information is mostly due to the lack of an assay system in which the kinetics of astrocyte- and microglia-mediated phagocytosis are easily comparable. To achieve this goal, we have developed a long-term live-imaging in vitro phagocytosis assay to evaluate the phagocytic capacity of purified astrocytes and microglia. In this assay, real-time detection of engulfment and degradation is possible using pH indicator-conjugated synaptosomes, which emit bright red fluorescence in acidic organelles, such as lysosomes. Our novel assay provides simple and effective detection of phagocytosis through live-imaging. In addition, this in vitro phagocytosis assay can be used as a screening platform to identify chemicals and compounds that can enhance or inhibit the phagocytic capacity of astrocytes. As synaptic pruning malfunction and pathogenic protein accumulation have been shown to cause mental disorders or neurodegenerative diseases, chemicals and compounds that modulate the phagocytic capacity of glial cells should be helpful in treating various neurological disorders.
星形胶质细胞是大脑中的主要细胞类型,直接与突触和血管接触。尽管小胶质细胞一直被认为是大脑中的主要免疫细胞且是唯一的吞噬细胞,但最近的研究表明,星形胶质细胞也参与各种吞噬过程,如发育过程中的突触消除以及阿尔茨海默病(AD)中β淀粉样蛋白斑块的清除。尽管有这些发现,但与小胶质细胞相比,星形胶质细胞吞噬和降解其靶标的效率尚不清楚。这种信息缺失主要是由于缺乏一种能够轻松比较星形胶质细胞和小胶质细胞介导的吞噬作用动力学的检测系统。为了实现这一目标,我们开发了一种长期实时成像的体外吞噬试验,以评估纯化的星形胶质细胞和小胶质细胞的吞噬能力。在该试验中,使用与pH指示剂偶联的突触小体可以实时检测吞噬和降解过程,这些突触小体在酸性细胞器(如溶酶体)中发出亮红色荧光。我们的新试验通过实时成像提供了简单有效的吞噬作用检测方法。此外,这种体外吞噬试验可以用作筛选平台,以鉴定能够增强或抑制星形胶质细胞吞噬能力的化学物质和化合物。由于突触修剪功能障碍和致病蛋白积累已被证明会导致精神障碍或神经退行性疾病,调节胶质细胞吞噬能力的化学物质和化合物应该有助于治疗各种神经系统疾病。