Lange Markus, Prassler Jana, Ecke Mary, Müller-Taubenberger Annette, Gerisch Günther
Max Planck Institute of Biochemistry, Am Klopferspitz 18, Martinsried D-82152, Germany.
LMU Munich, Department of Cell Biology (Anatomy III), BioMedical Center, Großhaderner Str. 9, Martinsried D-82152, Germany.
J Cell Sci. 2016 Sep 15;129(18):3462-72. doi: 10.1242/jcs.191148. Epub 2016 Aug 5.
Chemotactic responses of eukaryotic cells require a signal processing system that translates an external gradient of attractant into directed motion. To challenge the response system to its limits, we increased the size of Dictyostelium discoideum cells by using electric-pulse-induced fusion. Large cells formed multiple protrusions at different sites along the gradient of chemoattractant, independently turned towards the gradient and competed with each other. Finally, these cells succeeded to re-establish polarity by coordinating front and tail activities. To analyse the responses, we combined two approaches, one aimed at local responses by visualising the dynamics of Ras activation at the front regions of reorientating cells, the other at global changes of polarity by monitoring front-to-tail-directed actin flow. Asymmetric Ras activation in turning protrusions underscores that gradients can be sensed locally and translated into orientation. Different to cells of normal size, the polarity of large cells is not linked to an increasing front-to-tail gradient of the PIP3-phosphatase PTEN. But even in large cells, the front communicates with the tail through an actin flow that might act as carrier of a protrusion inhibitor.
真核细胞的趋化反应需要一个信号处理系统,该系统将外部趋化因子梯度转化为定向运动。为了将反应系统挑战到极限,我们通过电脉冲诱导融合增加了盘基网柄菌细胞的大小。大细胞在趋化因子梯度的不同位置形成多个突起,独立转向梯度并相互竞争。最后,这些细胞通过协调前端和后端活动成功重新建立了极性。为了分析这些反应,我们结合了两种方法,一种通过可视化重新定向细胞前端区域的Ras激活动力学来研究局部反应,另一种通过监测从前到后的肌动蛋白流来研究极性的全局变化。转向突起中不对称的Ras激活强调了梯度可以在局部被感知并转化为定向。与正常大小的细胞不同,大细胞的极性与PIP3磷酸酶PTEN从前到后的梯度增加无关。但即使在大细胞中,前端也通过肌动蛋白流与后端进行通信,肌动蛋白流可能充当突起抑制剂的载体。