Grebecki A, Kłopocka W
J Cell Sci. 1981 Aug;50:245-58. doi: 10.1242/jcs.50.1.245.
Polytactic cells of Amoeba proteus were exposed to localized photic stimulation. When a pseudopodium is stimulated to advance, by shading it, other pseudopodia are retracted. Activation of the shaded front is the primary response, and contraction of other fronts the secondary one. When a pseudopodium is inhibited by illuminating its frontal segment, or when it is allowed to enter the bright zone in the course of migration, it slows down and stops but its eventual retraction depends on the existence of other possible directions for the endoplasmic flow. Therefore, if other active pseudopodia are lacking, the front suppressed by light cannot retreat effectively until new fronts arise in other body regions kept in shade. In all experimental situations the development of new fronts or the activation of forward flow in lateral pseudopodia precedes the contraction of the former leading pseudopodium. Also the reversal of direction of the endoplasmic streaming begins at the new front, and then it gradually extends until it reaches the former front. The results confirm the interdependence of different pseudopodia in the same individual and they contradict the concept that pseudopodia behave as separate functional units. On the other hand, they indicate that formation of new pseudopodia should not be explained as a simple secondary effect of contraction of the older ones but, on the contrary, as a phenomenon that initiates the changes in the pattern of flow in amoeba. The general interpretation is based on this variant of the pressure-flow theory of amoeboid movement, which attributes the motive power to the contractile activity of the whole cell cortex and the steering role to events taking place in the front of the migrating cell.
将变形虫的多伪足细胞暴露于局部光刺激下。当一个伪足通过遮光被刺激向前推进时,其他伪足会缩回。被遮光的前端的激活是主要反应,而其他前端的收缩是次要反应。当一个伪足通过照亮其前端部分而受到抑制时,或者当它在迁移过程中进入明亮区域时,它会减慢速度并停止,但它最终的缩回取决于内质流是否存在其他可能的方向。因此,如果没有其他活跃的伪足,被光抑制的前端就无法有效退缩,直到在其他处于阴影中的身体区域出现新的前端。在所有实验情况下,新前端的形成或侧伪足中向前流动的激活都先于先前主导伪足的收缩。内质流方向的逆转也始于新前端,然后逐渐扩展,直到到达先前的前端。这些结果证实了同一个体中不同伪足之间的相互依存关系,并且与伪足作为独立功能单元的概念相矛盾。另一方面,它们表明新伪足的形成不应被解释为较老伪足收缩的简单次要效应,相反,应被解释为一种引发变形虫流动模式变化的现象。一般解释基于变形虫运动压力流理论的这种变体,该理论将动力归因于整个细胞皮层的收缩活动,并将导向作用归因于迁移细胞前端发生的事件。