Rappel Wouter-Jan, Thomas Peter J, Levine Herbert, Loomis William F
Department of Physics, University of California, San Diego, La Jolla, California 92093-0319, USA.
Biophys J. 2002 Sep;83(3):1361-7. doi: 10.1016/S0006-3495(02)73906-4.
Several recent studies have demonstrated that eukaryotic cells, including amoeboid cells of Dictyostelium discoideum and neutrophils, respond to chemoattractants by translocation of PH-domain proteins to the cell membrane, where these proteins participate in the modulation of the cytoskeleton and relay of the signal. When the chemoattractant is released from a pipette, the localization is found predominantly on the proximal side of the cell. The recruitment of PH-domain proteins, particularly for Dictyostelium cells, occurs very rapidly (<2 s). Thus, the mechanism responsible for the first step in the directional sensing process of a cell must be able to establish an asymmetry on the same time scale. Here, we propose a simple mechanism in which a second messenger, generated by local activation of the membrane, diffuses through the interior of the cell, suppresses the activation of the back of the cell, and converts the temporal gradient into an initial cellular asymmetry. Numerical simulations show that such a mechanism is plausible. Available evidence suggests that the internal inhibitor may be cGMP, which accumulates within less than a second following treatment of cells with external cAMP.
最近的几项研究表明,包括盘基网柄菌的变形细胞和中性粒细胞在内的真核细胞,通过将PH结构域蛋白转运到细胞膜来对趋化因子作出反应,这些蛋白在细胞膜上参与细胞骨架的调节和信号传递。当趋化因子从移液器中释放出来时,其定位主要出现在细胞的近端。PH结构域蛋白的募集,特别是对于盘基网柄菌细胞来说,发生得非常迅速(<2秒)。因此,负责细胞定向感知过程第一步的机制必须能够在相同的时间尺度上建立不对称性。在这里,我们提出了一种简单的机制,即由膜的局部激活产生的第二信使扩散穿过细胞内部,抑制细胞后部的激活,并将时间梯度转化为初始的细胞不对称性。数值模拟表明这种机制是合理的。现有证据表明,内部抑制剂可能是环鸟苷酸(cGMP),在用外部环磷酸腺苷(cAMP)处理细胞后不到一秒钟内它就会积累。