Single-Molecule Tracking and Super-Resolution Microscopy Unveil Actin-Driven Membrane Nanotopography Shaping Stable Integrin Adhesions in Developing Tissue.

Tianchi Chen, Grégory Giannone
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Abstract

Single molecule tracking and super-resolution microscopy of integrin adhesion proteins and actin in developing Drosophila muscle attachment sites reveals that nanotopography triggered by Arp2/3-dependent actin protrusions promotes stable adhesion formation. The nanodomains formed during this process confine the diffusion of integrins and promote their immobilization. Spatial confinement is also applied to the motion of actin filaments, resulting in enhanced mechanical connection with the integrin adhesion complex. Fabricated nano-structured surfaces mimicking the nanotopography observed in living tissue are able to recapitulate the formation of these adhesions in isolated muscle cells and the confinement of integrin diffusion. These results emphasize the importance of geometrical regulation of tissue morphogenesis at a single molecule level.

单分子跟踪和超分辨率显微镜揭示肌动蛋白驱动的膜纳米形貌在发育组织中形成稳定的整合素粘附。
对发育中的果蝇肌肉附着位点的整合素粘附蛋白和肌动蛋白的单分子跟踪和超分辨率显微镜研究表明,arp2 /3依赖性肌动蛋白突起触发的纳米形貌促进了稳定的粘附形成。在此过程中形成的纳米结构域限制了整合素的扩散并促进了它们的固定化。空间限制也适用于肌动蛋白丝的运动,从而增强了与整合素粘附复合物的机械连接。合成的纳米结构表面模拟了在活组织中观察到的纳米形貌,能够在分离的肌肉细胞中再现这些粘连的形成和对整合素扩散的限制。这些结果强调了在单分子水平上组织形态发生的几何调控的重要性。
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