Amsterdam UMC, University of Amsterdam, Department of Medical Biochemistry, Amsterdam Cardiovascular Sciences, 1105 AZ, Amsterdam, The Netherlands.
J Cell Sci. 2024 Oct 15;137(20). doi: 10.1242/jcs.262041. Epub 2024 Oct 31.
Studies utilizing electron microscopy and live fluorescence microscopy have significantly enhanced our understanding of the molecular mechanisms that regulate junctional dynamics during homeostasis, development and disease. To fully grasp the enormous complexity of cell-cell adhesions, it is crucial to study the nanoscale architectures of tight junctions, adherens junctions and desmosomes. It is important to integrate these junctional architectures with the membrane morphology and cellular topography in which the junctions are embedded. In this Review, we explore new insights from studies using super-resolution and volume electron microscopy into the nanoscale organization of these junctional complexes as well as the roles of the junction-associated cytoskeleton, neighboring organelles and the plasma membrane. Furthermore, we provide an overview of junction- and cytoskeletal-related biosensors and optogenetic probes that have contributed to these advances and discuss how these microscopy tools enhance our understanding of junctional dynamics across cellular environments.
利用电子显微镜和活荧光显微镜的研究极大地提高了我们对调节连接子动态的分子机制的理解,这些连接子动态存在于稳态、发育和疾病过程中。为了充分理解细胞间黏附的巨大复杂性,研究紧密连接、黏着连接和桥粒的纳米级结构至关重要。将这些连接子结构与连接子所嵌入的膜形态和细胞拓扑结构整合起来也很重要。在这篇综述中,我们探讨了使用超高分辨率和体积电子显微镜研究这些连接子复合体的纳米级组织以及连接子相关细胞骨架、邻近细胞器和质膜的作用所获得的新见解。此外,我们还概述了与连接子和细胞骨架相关的生物传感器和光遗传学探针,这些探针对这些进展做出了贡献,并讨论了这些显微镜工具如何增强我们对跨细胞环境的连接子动态的理解。