Langridge Paul D, Kay Robert R
MRC Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 2QH, UK.
Exp Cell Res. 2006 Jul 1;312(11):2009-17. doi: 10.1016/j.yexcr.2006.03.007. Epub 2006 Apr 19.
Stimulation of Dictyostelium cells with a high uniform concentration of the chemoattractant cyclic-AMP induces a series of morphological changes, including cell rounding and subsequent extension of pseudopodia in random directions. Here we report that cyclic-AMP also elicits blebs and analyse their mechanism of formation. The surface area and volume of cells remain constant during blebbing indicating that blebs form by the redistribution of cytoplasm and plasma membrane rather than the exocytosis of internal membrane coupled to a swelling of the cell. Blebbing occurs immediately after a rapid rise and fall in submembraneous F-actin, but the blebs themselves contain little F-actin as they expand. A mutant with a partially inactivated Arp2/3 complex has a greatly reduced rise in F-actin content, yet shows a large increase in blebbing. This suggests that bleb formation is not enhanced by the preceding actin dynamics, but is actually inhibited by them. In contrast, cells that lack myosin-II completely fail to bleb. We conclude that bleb expansion is likely to be driven by hydrostatic pressure produced by cortical contraction involving myosin-II. As blebs are induced by chemoattractant, we speculate that hydrostatic pressure is one of the forces driving pseudopod extension during movement up a gradient of cyclic-AMP.
用高浓度且均匀的趋化因子环磷酸腺苷(cyclic-AMP)刺激盘基网柄菌细胞会诱导一系列形态变化,包括细胞变圆以及随后伪足向随机方向伸展。在此我们报告环磷酸腺苷还会引发气泡,并分析其形成机制。在形成气泡的过程中细胞的表面积和体积保持恒定,这表明气泡是通过细胞质和质膜的重新分布形成的,而非内膜外排并伴随细胞肿胀。气泡在膜下F-肌动蛋白快速上升和下降后立即出现,但气泡在扩张时自身几乎不含F-肌动蛋白。一种Arp2/3复合体部分失活的突变体F-肌动蛋白含量的上升大幅减少,但气泡形成却大幅增加。这表明气泡形成并非由先前的肌动蛋白动态变化增强,实际上是受到其抑制。相反,完全缺乏肌球蛋白-II的细胞完全无法形成气泡。我们得出结论,气泡扩张可能是由涉及肌球蛋白-II的皮质收缩产生的静水压力驱动的。由于气泡是由趋化因子诱导产生的,我们推测静水压力是在环磷酸腺苷梯度上升过程中驱动伪足伸展的力量之一。