Potts Emily M, Coppotelli Giuseppe, Ross Jaime M
George & Anne Ryan Institute for Neuroscience, College of Pharmacy, Department of Biomedical and Pharmaceutical Sciences, University of Rhode Island.
George & Anne Ryan Institute for Neuroscience, College of Pharmacy, Department of Biomedical and Pharmaceutical Sciences, University of Rhode Island; Department of Neuroscience, Biomedicum, Karolinska Institutet;
J Vis Exp. 2020 Aug 25(162). doi: 10.3791/61622.
Immunohistochemistry is a widely used technique to visualize specific tissue structures as well as protein expression and localization. Two alternative approaches are widely used to handle the tissue sections during the staining procedure, one approach consists of mounting the sections directly on glass slides, while a second approach, the free-floating, allows for fixed sections to be maintained and stained while suspended in solution. Although slide-mounted and free-floating approaches may yield similar results, the free-floating technique allows for better antibody penetration and thus should be the method of choice when thicker sections are to be used for 3D reconstruction of the tissues, for example when the focus of the experiment is to gain information on dendritic and axonal projections in brain regions. In addition, since the sections are kept in solution, a single aliquot can easily accommodate 30 to 40 sections, handling of which is less laborious, particularly in large-scale biomedical studies. Here, we illustrate how to apply the free-floating method to fluorescent immunohistochemistry staining, with a major focus on brain sections. We will also discuss how the free-floating technique can easily be modified to fit the individual needs of researchers and adapted to other tissues as well as other histochemical-based stainings, such as hematoxylin and eosin and cresyl violet, as long as tissue samples are properly fixed, typically with paraformaldehyde or formalin.
免疫组织化学是一种广泛应用的技术,用于可视化特定的组织结构以及蛋白质的表达和定位。在染色过程中,有两种常用的方法来处理组织切片,一种方法是将切片直接安装在载玻片上,而另一种方法,即游离漂浮法,允许在固定的切片悬浮于溶液中时进行染色。虽然载玻片安装法和游离漂浮法可能产生相似的结果,但游离漂浮技术能使抗体更好地渗透,因此当需要使用较厚的切片进行组织的三维重建时,例如当实验重点是获取脑区树突和轴突投射的信息时,游离漂浮法应是首选方法。此外,由于切片保存在溶液中,一份样品可以轻松容纳30至40个切片,处理起来不那么费力,特别是在大规模生物医学研究中。在这里,我们将说明如何将游离漂浮法应用于荧光免疫组织化学染色,主要侧重于脑切片。我们还将讨论如何轻松修改游离漂浮技术以满足研究人员的个性化需求,并适用于其他组织以及其他基于组织化学的染色方法,如苏木精和伊红染色以及甲酚紫染色,只要组织样本用多聚甲醛或福尔马林等进行适当固定即可。