Worth Daniel C, Parsons Maddy
Randall Division of Cell and Molecular Biophysics, Kings College London, New Hunts House, Guys Campus, London SE1 1UL, UK.
Int J Biochem Cell Biol. 2008;40(11):2397-409. doi: 10.1016/j.biocel.2008.04.008. Epub 2008 Apr 14.
Adhesion to the extracellular matrix (ECM) is a fundamental requirement for survival, differentiation and migration of numerous cell types during both embryonic development and adult homeostasis. Different types of adhesion structures have been classified in different cell types or tissue environments. The best studied of these are focal adhesions which are found on a wide variety of cell types and will be the main focus of this review. Many years of research into the control of adhesion has yielded a wealth of information regarding the complexity of protein composition of these critical points of cell:ECM contact. Moreover, it has emerged that adhesions are not only highly ordered, but also dynamic structures under tight spatial control at the subcellular level to enable localised responses to extracellular cues. However, it is only in the last decade that the relative dynamics of these adhesion proteins have been closely studied. Here we provide an overview of the imaging strategies that have been developed and implemented to study the intricacies and hierarchy of protein turnover within focal adhesions. The caveats of employing these imaging techniques, as well as future directions will also be discussed.
在胚胎发育和成人稳态过程中,与细胞外基质(ECM)的黏附是众多细胞类型生存、分化和迁移的基本要求。不同类型的黏附结构已在不同细胞类型或组织环境中分类。其中研究最深入的是黏着斑,它存在于多种细胞类型中,将是本综述的主要焦点。多年来对黏附控制的研究产生了大量关于这些细胞与ECM接触关键点蛋白质组成复杂性的信息。此外,已经发现黏附不仅高度有序,而且是亚细胞水平上受到严格空间控制的动态结构,以便对细胞外信号进行局部响应。然而,直到最近十年,这些黏附蛋白的相对动力学才得到深入研究。在这里,我们概述了为研究黏着斑内蛋白质周转的复杂性和层次结构而开发和实施的成像策略。还将讨论使用这些成像技术的注意事项以及未来方向。