Laboratoire Kastler Brossel, CNRS UMR 8552, Département de Physique et Institut de Biologie, Ecole normale supérieure, Université Pierre et Marie Curie-Paris 6, Paris, France.
Nat Nanotechnol. 2013 Mar;8(3):193-8. doi: 10.1038/nnano.2013.23. Epub 2013 Mar 3.
Many cell functions rely on the coordinated activity of signalling pathways at a subcellular scale. However, there are few tools capable of probing and perturbing signalling networks with a spatial resolution matching the intracellular dimensions of their activity patterns. Here we present a generic magnetogenetic approach based on the self-assembly of signalling complexes on the surface of functionalized magnetic nanoparticles inside living cells. The nanoparticles act as nanoscopic hot spots that can be displaced by magnetic forces and trigger signal transduction pathways that bring about a cell response. We applied this strategy to Rho-GTPases, a set of molecular switches known to regulate cell morphology via complex spatiotemporal patterns of activity. We demonstrate that the nanoparticle-mediated activation of signalling pathways leads to local remodelling of the actin cytoskeleton and to morphological changes.
许多细胞功能依赖于亚细胞尺度上信号通路的协调活动。然而,目前能够以与其活性模式的细胞内尺寸相匹配的空间分辨率探测和干扰信号网络的工具却寥寥无几。在这里,我们提出了一种基于信号复合物在活细胞内功能化磁性纳米粒子表面自组装的通用磁遗传学方法。这些纳米粒子可以作为纳米级热点,通过磁力发生位移,并触发信号转导途径,从而引起细胞反应。我们将这种策略应用于 Rho-GTPases,这是一组已知通过复杂的时空活性模式来调节细胞形态的分子开关。我们证明,纳米粒子介导的信号通路的激活会导致肌动蛋白细胞骨架的局部重塑和形态变化。