Keizer-Gunnink Ineke, Kortholt Arjan, Van Haastert Peter J M
Department of Molecular Cell Biology, University of Groningen, Haren, Netherlands.
J Cell Biol. 2007 May 21;177(4):579-85. doi: 10.1083/jcb.200611046.
During embryonic development, cell movement is orchestrated by a multitude of attractants and repellents. Chemoattractants applied as a gradient, such as cAMP with Dictyostelium discoideum or fMLP with neutrophils, induce the activation of phospholipase C (PLC) and phosphoinositide 3 (PI3)-kinase at the front of the cell, leading to the localized depletion of phosphatidylinositol 4,5-bisphosphate (PI[4,5]P(2)) and the accumulation of phosphatidylinositol-3,4,5-trisphosphate (PI[3,4,5]P(3)). Using D. discoideum, we show that chemorepellent cAMP analogues induce localized inhibition of PLC, thereby reversing the polarity of PI(4,5)P(2). This leads to the accumulation of PI(3,4,5)P(3) at the rear of the cell, and chemotaxis occurs away from the source. We conclude that a PLC polarity switch controls the response to attractants and repellents.
在胚胎发育过程中,细胞运动由多种吸引剂和排斥剂协调。作为梯度施加的化学吸引剂,如盘基网柄菌的环磷酸腺苷(cAMP)或中性粒细胞的N-甲酰甲硫氨酸-亮氨酸-苯丙氨酸(fMLP),会诱导细胞前端的磷脂酶C(PLC)和磷酸肌醇3(PI3)激酶激活,导致磷脂酰肌醇4,5-二磷酸(PI[4,5]P₂)局部消耗以及磷脂酰肌醇-3,4,5-三磷酸(PI[3,4,5]P₃)积累。利用盘基网柄菌,我们发现化学排斥性cAMP类似物会诱导PLC局部抑制,从而逆转PI(4,5)P₂的极性。这导致PI(3,4,5)P₃在细胞后端积累,细胞发生趋化运动远离源头。我们得出结论,PLC极性开关控制对吸引剂和排斥剂的反应。