Sun Chun Xiang, Magalhães Marco A O, Glogauer Michael
The Canadian Institutes of Health Research Group in Matrix Dynamics and Dental Research Institute, Faculty of Dentistry, University of Toronto, Toronto, Ontario, Canada M5G 1G6.
J Cell Biol. 2007 Oct 22;179(2):239-45. doi: 10.1083/jcb.200705122.
Actin assembly at the leading edge of migrating cells depends on the availability of high-affinity free barbed ends (FBE) that drive actin filament elongation and subsequent membrane protrusion. We investigated the specific mechanisms through which the Rac1 and Rac2 small guanosine triphosphatases (GTPases) generate free barbed ends in neutrophils. Using neutrophils lacking either Rac1 or Rac2 and a neutrophil permeabilization model that maintains receptor signaling to the actin cytoskeleton, we assessed the mechanisms through which these two small GTPases mediate FBE generation downstream of the formyl-methionyl-leucyl-phenylalanine receptor. We demonstrate here that uncapping of existing barbed ends is mediated through Rac1, whereas cofilin- and ARP2/3-mediated FBE generation are regulated through Rac2. This unique combination of experimental tools has allowed us to identify the relative roles of uncapping (15%), cofilin severing (10%), and ARP2/3 de novo nucleation (75%) in FBE generation and the respective roles played by Rac1 and Rac2 in mediating actin dynamics.
迁移细胞前沿的肌动蛋白组装依赖于高亲和力游离刺端(FBE)的可用性,这些刺端驱动肌动蛋白丝伸长及随后的膜突出。我们研究了Rac1和Rac2小GTP酶(GTPases)在中性粒细胞中产生游离刺端的具体机制。利用缺乏Rac1或Rac2的中性粒细胞以及维持受体向肌动蛋白细胞骨架信号传导的中性粒细胞透化模型,我们评估了这两种小GTP酶在甲酰甲硫氨酰亮氨酰苯丙氨酸受体下游介导FBE产生的机制。我们在此证明,现有刺端的去帽作用由Rac1介导,而丝切蛋白和ARP2/3介导的FBE产生则由Rac2调节。这种独特的实验工具组合使我们能够确定去帽(15%)、丝切蛋白切断(10%)和ARP2/3从头成核(75%)在FBE产生中的相对作用,以及Rac1和Rac2在介导肌动蛋白动力学中各自发挥的作用。