Tian Wei, Laffafian Iraj, Dewitt Sharon, Hallett Maurice B
Neutrophil Signalling Group, University Department of Surgery, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, UK.
EMBO Rep. 2003 Oct;4(10):982-8. doi: 10.1038/sj.embor.embor947.
Although there is accumulating evidence that the generation and localization of phosphatidylinositol-3,4,5-trisphosphate (PtdIns(3,4,5)P(3)) have important functions in neutrophil polarization and chemotaxis, the mechanism of this linkage has yet to be established. Here, using exogenous fluorescent PtdIns(3,4,5)P(3) introduced into the inner leaflet of the neutrophil plasma membrane by a cationic carrier, we show that: first, PtdIns(3,4,5)P(3) uniformly delivered to the neutrophil plasma membrane is excluded from newly forming pseudopodia; second, PtdIns(3,4,5)P(3) translocates to and is immobilized at the pole opposite a stable polarizing pseudopod; third, asymmetric delivery of PtdIns(3,4,5)P(3) to the neutrophil triggers the generation of polarizing pseudopodia at the opposite pole; and finally, PtdIns(3,4,5)P(3) triggers repetitive Ca(2+) signals, the onset of which precedes morphological polarization. These data suggest that translocation and immobilization of PtdIns(3,4,5)P(3) or a 3,x-phosphorylated metabolite in the uropod functions as an important polarization cue that defines neutrophil polarity and stabilizes the generation of pseudopodia at the opposite pole.
尽管越来越多的证据表明磷脂酰肌醇-3,4,5-三磷酸(PtdIns(3,4,5)P(3))的生成和定位在中性粒细胞极化和趋化作用中具有重要功能,但这种联系的机制尚未确立。在此,我们通过阳离子载体将外源性荧光PtdIns(3,4,5)P(3)引入中性粒细胞质膜的内小叶,结果表明:第一,均匀递送至中性粒细胞质膜的PtdIns(3,4,5)P(3)被新形成的伪足排除;第二,PtdIns(3,4,5)P(3)转位至稳定极化伪足相对的极并固定在该处;第三,向中性粒细胞不对称递送PtdIns(3,4,5)P(3)会在相对的极触发极化伪足的生成;最后,PtdIns(3,4,5)P(3)触发重复性Ca(2+)信号,其起始先于形态极化。这些数据表明,PtdIns(3,4,5)P(3)或尾足中3,x-磷酸化代谢物的转位和固定作为一种重要的极化信号,可定义中性粒细胞极性并稳定相对极伪足的生成。