VIB-KU Leuven Center for Brain & Disease Research, Electron Microscopy Platform & VIB-Bioimaging Core, O&N4 Herestraat 49 box 602, 3000, Leuven, Belgium.
KU Leuven Department of Neurosciences, Leuven Brain Institute, O&N4 Herestraat 49 box 602, 3000, Leuven, Belgium.
Sci Rep. 2019 Jan 15;9(1):130. doi: 10.1038/s41598-018-37377-x.
Analysis of neuronal arborization and connections is a powerful tool in fundamental and clinical neuroscience. Changes in neuronal morphology are central to brain development and plasticity and are associated with numerous diseases. Golgi staining is a classical technique based on a deposition of metal precipitate in a random set of neurons. Despite their versatility, Golgi methods have limitations that largely precluded their use in advanced microscopy. We combined Golgi staining with fluorescent labeling and tissue clearing techniques in an Alzheimer's disease model. We further applied 3D electron microscopy to visualize entire Golgi-stained neurons, while preserving ultrastructural details of stained cells, optimized Golgi staining for use with block-face scanning electron microscopy, and developed an algorithm for semi-automated neuronal tracing of cells displaying complex staining patterns. Our method will find use in fundamental neuroscience and the study of neuronal morphology in disease.
神经元分支和连接的分析是基础和临床神经科学的有力工具。神经元形态的变化是大脑发育和可塑性的核心,与许多疾病有关。高尔基染色是一种经典技术,基于随机一组神经元中的金属沉淀沉积。尽管它们用途广泛,但高尔基方法有其局限性,在很大程度上排除了它们在高级显微镜中的使用。我们将高尔基染色与荧光标记和组织透明技术结合在阿尔茨海默病模型中。我们进一步应用 3D 电子显微镜来可视化整个高尔基染色的神经元,同时保留染色细胞的超微结构细节,优化了高尔基染色用于块面扫描电子显微镜,并开发了一种算法,用于对显示复杂染色模式的细胞进行半自动神经元追踪。我们的方法将在基础神经科学和疾病中神经元形态的研究中得到应用。