Van Keymeulen Alexandra, Wong Kit, Knight Zachary A, Govaerts Cedric, Hahn Klaus M, Shokat Kevan M, Bourne Henry R
Department of Cellular and Molecular Pharmacology, and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA.
J Cell Biol. 2006 Jul 31;174(3):437-45. doi: 10.1083/jcb.200604113. Epub 2006 Jul 24.
Chemoattractants like f-Met-Leu-Phe (fMLP) induce neutrophils to polarize by triggering divergent signals that promote the formation of protrusive filamentous actin (F-actin; frontness) and RhoA-dependent actomyosin contraction (backness). Frontness locally inhibits backness and vice versa. In neutrophil-like HL60 cells, blocking phosphatidylinositol-3,4,5-tris-phosphate (PIP3) accumulation with selective inhibitors of PIP3 synthesis completely prevents fMLP from activating a PIP3-dependent kinase and Cdc42 but not from stimulating F-actin accumulation. PIP3-deficient cells show reduced fMLP-dependent Rac activity and unstable pseudopods, which is consistent with the established role of PIP3 as a mediator of positive feedback pathways that augment Rac activation at the front. Surprisingly, such cells also show reduced RhoA activation and RhoA-dependent contraction at the trailing edge, leading to the formation of multiple lateral pseudopods. Cdc42 mediates PIP3's positive effect on RhoA activity. Thus, PIP3 and Cdc42 maintain stable polarity with a single front and a single back not only by strengthening pseudopods but also, at longer range, by promoting RhoA-dependent actomyosin contraction at the trailing edge.
像甲酰甲硫氨酸-亮氨酸-苯丙氨酸(fMLP)这样的趋化因子通过触发不同信号诱导中性粒细胞极化,这些信号促进突出的丝状肌动蛋白(F-肌动蛋白;前沿)的形成以及RhoA依赖的肌动球蛋白收缩(后端)。前沿局部抑制后端,反之亦然。在类中性粒细胞HL60细胞中,用PIP3合成的选择性抑制剂阻断磷脂酰肌醇-3,4,5-三磷酸(PIP3)的积累可完全阻止fMLP激活PIP3依赖的激酶和Cdc42,但不能阻止其刺激F-肌动蛋白积累。缺乏PIP3的细胞显示出fMLP依赖的Rac活性降低和伪足不稳定,这与PIP3作为增强前沿Rac激活的正反馈途径的介质的既定作用一致。令人惊讶的是,这类细胞在尾端也显示出RhoA激活和RhoA依赖的收缩减少,导致形成多个侧向伪足。Cdc42介导PIP3对RhoA活性的正向作用。因此,PIP3和Cdc42不仅通过加强伪足,而且在更远的范围内通过促进尾端RhoA依赖的肌动球蛋白收缩来维持具有单个前沿和单个后端的稳定极性。