McKenzie Andrew T, Woodoff-Leith Emma, Dangoor Diana, Cervera Alessandra, Ressler Hadley Walsh, Whitney Kristen, Dams-O'Connor Kristen, Wu Zhuhao, Hillman Elizabeth M C, Seifert Alan C, Crary John F
Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Friedman Brain Institute, Departments of Pathology, Neuroscience, and Artificial Intelligence & Human Health, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Free Neuropathol. 2022 Sep 28;3:22. doi: 10.17879/freeneuropathology-2022-4368. eCollection 2022 Jan.
Perfusion fixation is a well-established technique in animal research to improve preservation quality in the study of many tissues, including the brain. There is a growing interest in using perfusion to fix postmortem human brain tissue to achieve the highest fidelity preservation for downstream high-resolution morphomolecular brain mapping studies. Numerous practical barriers arise when applying perfusion fixation in brain banking settings, including the large mass of the organ, degradation of vascular integrity and patency prior to the start of the procedure, and differing investigator goals sometimes necessitating part of the brain to be frozen. As a result, there is a critical need to establish a perfusion fixation procedure in brain banking that is flexible and scalable. This technical report describes our approach to developing an perfusion fixation protocol. We discuss the challenges encountered and lessons learned while implementing this procedure. Routine morphological staining and RNA hybridization data show that the perfused brains have well-preserved tissue cytoarchitecture and intact biomolecular signal. However, it remains uncertain whether this procedure leads to improved histology quality compared to immersion fixation. Additionally, magnetic resonance imaging (MRI) data suggest that the perfusion fixation protocol may introduce imaging artifacts in the form of air bubbles in the vasculature. We conclude with further research directions to investigate the use of perfusion fixation as a rigorous and reproducible alternative to immersion fixation for the preparation of postmortem human brains.
灌注固定是动物研究中一种成熟的技术,可提高包括大脑在内的许多组织研究中的保存质量。越来越多的人关注使用灌注来固定死后的人类脑组织,以便在下游的高分辨率形态分子脑图谱研究中实现最高保真度的保存。在脑库环境中应用灌注固定时会出现许多实际障碍,包括器官体积大、在程序开始前血管完整性和通畅性下降,以及不同研究者的目标有时需要将部分大脑冷冻。因此,迫切需要在脑库中建立一种灵活且可扩展的灌注固定程序。本技术报告描述了我们开发灌注固定方案的方法。我们讨论了实施该程序时遇到的挑战和吸取的教训。常规形态学染色和RNA杂交数据表明,灌注后的大脑具有保存良好的组织细胞结构和完整的生物分子信号。然而,与浸泡固定相比,该程序是否能提高组织学质量仍不确定。此外,磁共振成像(MRI)数据表明,灌注固定方案可能会在血管系统中引入气泡形式的成像伪影。我们最后提出了进一步的研究方向,以探讨将灌注固定作为浸泡固定的一种严格且可重复的替代方法用于死后人类大脑的制备。