Centre de Cancérologie de Marseille, Équipe "Interactions Leuco/Stromales", Institut Paoli-Calmettes, Institut National de la Santé et de la Recherche Médicale U1068, Centre National de la Recherche Scientifique UMR7258, Aix-Marseille Université UM105 Marseille, France.
Front Cell Dev Biol. 2016 May 4;4:36. doi: 10.3389/fcell.2016.00036. eCollection 2016.
The plasma membrane delimits the cell, which is the basic unit of living organisms, and is also a privileged site for cell communication with the environment. Cell adhesion can occur through cell-cell and cell-matrix contacts. Adhesion proteins such as integrins and cadherins also constitute receptors for inside-out and outside-in signaling within proteolipidic platforms. Adhesion molecule targeting and stabilization relies on specific features such as preferential segregation by the sub-membrane cytoskeleton meshwork and within membrane proteolipidic microdomains. This review presents an overview of the recent insights brought by the latest developments in microscopy, to unravel the molecular remodeling occurring at cell contacts. The dynamic aspect of cell adhesion was recently highlighted by super-resolution videomicroscopy, also named videonanoscopy. By circumventing the diffraction limit of light, nanoscopy has allowed the monitoring of molecular localization and behavior at the single-molecule level, on fixed and living cells. Accessing molecular-resolution details such as quantitatively monitoring components entering and leaving cell contacts by lateral diffusion and reversible association has revealed an unexpected plasticity. Adhesion structures can be highly specialized, such as focal adhesion in motile cells, as well as immune and neuronal synapses. Spatiotemporal reorganization of adhesion molecules, receptors, and adaptors directly relates to structure/function modulation. Assembly of these supramolecular complexes is continuously balanced by dynamic events, remodeling adhesions on various timescales, notably by molecular conformation switches, lateral diffusion within the membrane and endo/exocytosis. Pathological alterations in cell adhesion are involved in cancer evolution, through cancer stem cell interaction with stromal niches, growth, extravasation, and metastasis.
细胞膜界定了细胞,细胞是生物体的基本单位,也是细胞与环境进行通讯的特权场所。细胞黏附可以通过细胞-细胞和细胞-基质接触发生。黏附蛋白,如整合素和钙黏蛋白,也是质膜蛋白平台内的内-外信号和外-内信号的受体。黏附分子的靶向和稳定依赖于特定的特征,如通过亚膜细胞骨架网格和膜内质膜微区的优先分隔。这篇综述介绍了显微镜最新发展带来的最新见解,以揭示细胞接触处发生的分子重塑。细胞黏附的动态方面最近被超分辨率视频显微镜(也称为视频纳米镜)强调。通过绕过光的衍射极限,纳米显微镜允许在固定和活细胞上以单分子水平监测分子定位和行为。访问分子分辨率的细节,如通过侧向扩散和可逆结合定量监测进入和离开细胞接触的组件,揭示了意想不到的可塑性。黏附结构可以高度特化,如运动细胞中的粘着斑,以及免疫和神经元突触。黏附分子、受体和衔接蛋白的时空重排直接与结构/功能调节相关。这些超分子复合物的组装不断受到动态事件的平衡,通过分子构象转换、膜内侧向扩散和内吞/胞吐作用在各种时间尺度上重塑黏附。细胞黏附的病理性改变参与了癌症的演变,通过癌症干细胞与基质龛、生长、血管外渗和转移的相互作用。