Program in Cellular and Molecular Biology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Dev Cell. 2010 Feb 16;18(2):226-36. doi: 10.1016/j.devcel.2009.11.015.
Cell polarity is crucial for directed migration. Here we show that phosphoinositide 3-kinase (PI(3)K) mediates neutrophil migration in vivo by differentially regulating cell protrusion and polarity. The dynamics of PI(3)K products PI(3,4,5)P(3)-PI(3,4)P(2) during neutrophil migration were visualized in living zebrafish, revealing that PI(3)K activation at the leading edge is critical for neutrophil motility in intact tissues. A genetically encoded photoactivatable Rac was used to demonstrate that localized activation of Rac is sufficient to direct migration with precise temporal and spatial control in vivo. Similar stimulation of PI(3)K-inhibited cells did not direct migration. Localized Rac activation rescued membrane protrusion but not anteroposterior polarization of F-actin dynamics of PI(3)K-inhibited cells. Uncoupling Rac-mediated protrusion and polarization suggests a paradigm of two-tiered PI(3)K-mediated regulation of cell motility. This work provides new insight into how cell signaling at the front and back of the cell is coordinated during polarized cell migration in intact tissues within a multicellular organism.
细胞极性对于定向迁移至关重要。在这里,我们表明,磷酸肌醇 3-激酶(PI(3)K)通过差异调节细胞突起和极性来介导体内中性粒细胞的迁移。在活体斑马鱼中可视化了中性粒细胞迁移过程中 PI(3)K 产物 PI(3,4,5)P(3)-PI(3,4)P(2)的动力学,揭示了在完整组织中,PI(3)K 在前缘的激活对于中性粒细胞的运动至关重要。使用遗传编码的光活化 Rac 来证明,局部激活 Rac 足以在体内进行具有精确时空控制的定向迁移。对 PI(3)K 抑制细胞的类似刺激不能指导迁移。局部 Rac 激活挽救了 PI(3)K 抑制细胞的膜突起,但不能挽救 F-肌动蛋白动力学的前后极化。 Rac 介导的突起和极化的解耦表明,细胞信号转导在完整组织中极性细胞迁移的 PI(3)K 介导的调节中存在两层范式。这项工作为细胞在多细胞生物体的完整组织中进行极化迁移时,如何协调细胞前后端的细胞信号提供了新的见解。