Sajman Julia, Sherman Eilon
Racah Institute of Physics, The Hebrew University, Jerusalem, Israel.
Jerusalem College of technology, Jerusalem, Israel.
Methods Mol Biol. 2023;2654:149-158. doi: 10.1007/978-1-0716-3135-5_10.
Physical interfaces mediate interactions between multiple types of cells. Despite the importance of such interfaces to the cells' function, their high-resolution optical imaging has been typically limited due to poor alignment of the interfaces relative to the optical plane of imaging. Here, we present a simple and robust method to align cell-cell interfaces in parallel to the coverslip by adhering the interacting cells to two opposing coverslips and bringing them into contact in a controlled and stable fashion. We demonstrate aberration-free high-resolution imaging of interfaces between live T cells and antigen-presenting cells, known as immune synapses, as an outstanding example. Imaging methods may include multiple diffraction-limited and super-resolution microscopy techniques (e.g., bright-field, confocal, STED, and dSTORM). Thus, our simple and widely compatible approach allows imaging with high- and super-resolution the intricate structure and molecular organization within a variety of cell-cell interfaces.
物理界面介导多种类型细胞之间的相互作用。尽管这种界面对于细胞功能很重要,但由于界面相对于成像光学平面的对准不佳,其高分辨率光学成像通常受到限制。在这里,我们提出了一种简单而稳健的方法,通过将相互作用的细胞粘附到两个相对的盖玻片上,并以可控和稳定的方式使它们接触,从而将细胞 - 细胞界面与盖玻片平行对齐。作为一个突出的例子,我们展示了活T细胞与抗原呈递细胞之间界面(即免疫突触)的无像差高分辨率成像。成像方法可能包括多种衍射极限和超分辨率显微镜技术(例如明场、共聚焦、受激发射损耗显微镜和直接随机光学重建显微镜)。因此,我们这种简单且广泛兼容的方法允许以高分辨率和超分辨率对各种细胞 - 细胞界面内的复杂结构和分子组织进行成像。