Cheng Ruoyu, Zhang Feng, Li Meng, Wo Xiang, Su Yu-Wen, Wang Wei
State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China.
Department of Monoclonal Antibody Products, National Institutes for Food and Drug Control, Beijing, China.
Front Chem. 2019 Aug 23;7:588. doi: 10.3389/fchem.2019.00588. eCollection 2019.
Fixation and permeabilization of cells and tissues are essential processes in biological techniques like immunofluorescence and immunohistochemistry for cell biology studies. In typical procedures, the biological samples are treated by paraformaldehyde and Triton X-100 to achieve cellular fixation and permeabilization, respectively, prior to the incubation with specific antibodies. While it is well-known that the integrity of cell membrane has been broken during these processes, quantitative studies on the loss of cellular mass density and the enhancement of molecular accessibility at single cell level are still rare. In this study, we employed the surface plasmon resonance (SPR) imaging technique to monitor the mass density change of single cells during sequential fixation and permeabilization processes. We further utilize the osmotic responses of single cells to sugar molecules as an indicator to evaluate the integrity of cell membranes. It was found that, while fixation initially destructed the integrity of cell membranes and increased the permeability of intra- and extra-cellular molecules, it was permeabilization process that substantially induced significant loss in cellular mass density.
细胞和组织的固定与通透处理是细胞生物学研究中免疫荧光和免疫组织化学等生物技术的关键步骤。在典型的实验流程中,生物样本先用多聚甲醛处理以实现细胞固定,再用 Triton X - 100 处理以实现细胞通透,然后才与特异性抗体孵育。虽然众所周知在这些过程中细胞膜的完整性会被破坏,但在单细胞水平上对细胞质量密度损失和分子可及性增强进行定量研究仍然很少见。在本研究中,我们采用表面等离子体共振(SPR)成像技术来监测单细胞在连续固定和通透处理过程中的质量密度变化。我们进一步利用单细胞对糖分子的渗透反应作为指标来评估细胞膜的完整性。结果发现,虽然固定最初破坏了细胞膜的完整性并增加了细胞内和细胞外分子的通透性,但真正导致细胞质量密度显著损失的是通透处理过程。