Konno Kohtarou, Yamasaki Miwako, Watanabe Masahiko
Department of Anatomy, Faculty of Medicine, Hokkaido University, Sapporo, 060-8638, Japan.
Anat Sci Int. 2025 May 26. doi: 10.1007/s12565-025-00848-z.
Chemical fixation is essential in immunohistochemistry for detecting molecular localization. The gold-standard fixative for immunohistochemistry is 4% paraformaldehyde (PFA); however, its properties-such as tissue shrinkage and protein cross-linking through methylene bridges-often restrict antibody access, posing challenges to achieving specific binding reactions. This is particularly true for receptors and ion channels condensed in the synaptic cleft, postsynaptic density, or trigger zone of action potentials. To overcome this problem, several laboratories have attempted antigen-exposure techniques. Recently, we demonstrated that fixation by glyoxal, a dialdehyde with two carbon atoms, enables specific detection of molecular groups that are difficult to be detected in PFA-fixed tissues. Here, we summarize the advantages and precautions in the use of glyoxal fixative.
在免疫组织化学中,化学固定对于检测分子定位至关重要。免疫组织化学的金标准固定剂是4%多聚甲醛(PFA);然而,其特性,如组织收缩以及通过亚甲基桥进行蛋白质交联,常常会限制抗体的进入,给实现特异性结合反应带来挑战。对于浓缩在突触间隙、突触后致密区或动作电位触发区的受体和离子通道而言,情况尤其如此。为克服这一问题,多个实验室尝试了抗原暴露技术。最近,我们证明,使用乙二醛(一种含有两个碳原子的二醛)进行固定,能够特异性检测在PFA固定组织中难以检测到的分子基团。在此,我们总结了使用乙二醛固定剂的优点及注意事项。