State Key Laboratory of Medical Neurobiology and Institute of Brain Science, Brain Science Collaborative Innovation Center, Fudan University, Shanghai, 200032, China.
Department of Integrative Medicine and Neurobiology, School of Basic Medical Sciences, Shanghai Medical College, Institutes of Integrative Medicine of Fudan University, Shanghai, 200032, China.
Sci Rep. 2017 Aug 29;7(1):9895. doi: 10.1038/s41598-017-10204-5.
Fast Free-of-Acrylamide Clearing Tissue (FACT) is a new sodium dodecyl sulfate (SDS)-based clearing protocol for the chemical clearing and imaging of brain tissue containing transgenic or immunolabeled fluorescent proteins. In the present study, we have developed this new method and optimized multiple dimensions of the workflow, including reduced clearing time, improved efficiency of fluorescent signals without the need for electrophoretic or complex instrumentations, preservation of cytoarchitectural details, optimized confocal microscopy, and accelerated data collection. We systematically compared seven clearing protocols with the FACT protocol, using transgenic mouse brains with fluorochrome expression in microglia. Only six days were required for detecting transgene-labeled markers in a 1-mm thick brain slice from adult mice, and 14 days were required for detecting antibody-labeled markers in the same-sized tissue. Preservation of fluorescent signal was achieved by decreasing clearing time, adjusting the pH of the SDS solution, and using the appropriate temperature for tissue clearing, all of which contributed to the superiority of our method. We conclude that the FACT protocol can be successfully applied to the fluorescent imaging of mouse brain tissue, and will facilitate structural analyses and connectomics of large assemblies of cells and their networks in the context of three-dimensional organ systems.
快速无丙烯酰胺组织透明化技术(Fast Free-of-Acrylamide Clearing Tissue,FACT)是一种新型的基于十二烷基硫酸钠(Sodium dodecyl sulfate,SDS)的组织透明化技术,可用于含有转染或免疫荧光标记的荧光蛋白的脑组织的化学透明化和成像。在本研究中,我们开发了这种新方法,并对其工作流程的多个方面进行了优化,包括缩短了透明化时间、提高了荧光信号的效率,而无需电泳或复杂的仪器、保持了细胞构筑的细节、优化了共聚焦显微镜和加速了数据采集。我们系统地比较了七种透明化方案与 FACT 方案,使用在小胶质细胞中表达荧光染料的转基因小鼠大脑。仅需 6 天即可检测到成年小鼠 1mm 厚脑片中的转基因标记物,而相同大小的组织中检测抗体标记物则需要 14 天。通过缩短透明化时间、调整 SDS 溶液的 pH 值以及使用适当的组织透明化温度,实现了荧光信号的保存,这些都有助于提高我们方法的优越性。我们得出结论,FACT 方案可成功应用于小鼠脑组织的荧光成像,将有助于在三维器官系统中对大量细胞及其网络的结构分析和连接组学研究。