Turku Bioscience Centre, University of Turku and Åbo Akademi University, FI-20520 Turku, Finland; InFLAMES Research Flagship Center, University of Turku, Turku, Finland.
Turku Bioscience Centre, University of Turku and Åbo Akademi University, FI-20520 Turku, Finland; InFLAMES Research Flagship Center, University of Turku, Turku, Finland; Department of Life Technologies, University of Turku, FI-20520 Turku, Finland; Western Finnish Cancer Center (FICAN West), University of Turku, FI-20520 Turku, Finland; Foundation for the Finnish Cancer Institute, Tukholmankatu 8, FI-00014 Helsinki, Finland.
Curr Opin Cell Biol. 2024 Jun;88:102355. doi: 10.1016/j.ceb.2024.102355. Epub 2024 Apr 16.
Integrin-mediated cell adhesion is essential for cell migration, mechanotransduction and tissue integrity. In vivo, these processes are regulated by complex physicochemical signals from the extracellular matrix (ECM). These nuanced cues, including molecular composition, rigidity and topology, call for sophisticated systems to faithfully explore cell behaviour. Here, we discuss recent methodological advances in cell-ECM adhesion research and compile a toolbox of techniques that we expect to shape this field in future. We outline methodological breakthroughs facilitating the transition from rigid 2D substrates to more complex and dynamic 3D systems, as well as advances in super-resolution imaging for an in-depth understanding of adhesion nanostructure. Selected methods are exemplified with relevant biological findings to underscore their applicability in cell adhesion research. We expect this new "toolbox" of methods will allow for a closer approximation of in vitro experimental setups to in vivo conditions, providing deeper insights into physiological and pathophysiological processes associated with cell-ECM adhesion.
整合素介导的细胞黏附对于细胞迁移、力学转导和组织完整性至关重要。在体内,这些过程受到细胞外基质 (ECM) 中复杂的物理化学信号的调节。这些细微的线索,包括分子组成、刚性和拓扑结构,需要复杂的系统来准确地探索细胞行为。在这里,我们讨论了细胞-ECM 黏附研究的最新方法学进展,并编写了一个技术工具包,我们预计这些技术将在未来塑造这个领域。我们概述了促进从刚性 2D 基质向更复杂和动态 3D 系统转变的方法学突破,以及超分辨率成像技术的进步,以深入了解黏附的纳米结构。选定的方法结合了相关的生物学发现,以强调它们在细胞黏附研究中的适用性。我们预计这个新的“工具包”方法将使体外实验装置更接近体内条件,从而更深入地了解与细胞-ECM 黏附相关的生理和病理生理过程。