Bültmann B D, Gruler H
J Cell Biol. 1983 Jun;96(6):1708-16. doi: 10.1083/jcb.96.6.1708.
The directed movement of human polymorphonuclear leukocytes (PMN) in a plane (Zigmond chamber assay) is described by a statistical model. We demonstrate that (a) the movement of a single cell is a superposition of a directed and a random movement, and (b) the degree of orientation, P1, of moving cells in a chemotactic gradient can be determined either by the time average of a single cell or by the average of movement of multiple cells at a fixed time (Ergoden hypothesis). However, an homogeneous cell population is a necessary condition. P1, which is identical with the McCutcheon index, is derived from the measured angular distribution function of moving cells. The statistical model allows one to distinguish between chemotaxis and chemokinesis. Applying this model to the temperature-dependent changes of cell movement, we found that P1 = 0.82 (37 degrees C) decreased to P1 = 0.4 (22 degrees C). The average speed of moving cells exhibits a very strong temperature-dependent variation from 30 microns/min (37 degrees C) to 5 microns/min (22 degrees C), indicating a different temperature dependence of chemotaxis and chemokinesis. At a fixed temperature (37 degrees C) the stability of the chemotactic gradient can also be checked by the angular distribution function. In addition, this model was applied to investigate the enteric cytopathogenic human orphan, strain 9 (ECHO 9) virus-induced disturbances of cell movement. We found: (a) The average speed of cell movement is not affected by the virus. (b) The degree of orientation is not affected for virus doses below a critical virus dose, ao (virus/PMN = 0.8:1). (c) The degree of orientation above this critical value exhibits a time- and virus-dose-dependence. (d) At a fixed viral dose, the time-dependent decrease of P1 is described by an exponential law (virus/PMN = 5:1, the characteristic time is 110 min). (e) This characteristic time investigated as a function of viral dose results in a logarithmic law analogous with the Weber-Fechner law. These findings indicate that only chemotactic and not chemokinetic response is disturbed by ECHO 9 virus.
一种统计模型描述了人多形核白细胞(PMN)在平面内的定向运动(齐格蒙德小室试验)。我们证明:(a)单个细胞的运动是定向运动和随机运动的叠加;(b)趋化梯度中运动细胞的定向程度P1,既可以通过单个细胞的时间平均值来确定,也可以通过固定时间多个细胞运动的平均值来确定(遍历假说)。然而,细胞群体均匀是一个必要条件。P1与麦卡琴指数相同,它由测量的运动细胞角度分布函数得出。该统计模型能让人区分趋化作用和化学增活现象。将此模型应用于细胞运动的温度依赖性变化,我们发现P1 = 0.82(37℃)降至P1 = 0.4(22℃)。运动细胞的平均速度呈现出非常强烈的温度依赖性变化,从30微米/分钟(37℃)降至5微米/分钟(22℃),这表明趋化作用和化学增活现象对温度的依赖性不同。在固定温度(37℃)下,趋化梯度的稳定性也可以通过角度分布函数来检查。此外,该模型被用于研究肠道致细胞病变人孤儿病毒9型(ECHO 9)诱导的细胞运动紊乱。我们发现:(a)细胞运动的平均速度不受病毒影响。(b)低于临界病毒剂量ao(病毒/PMN = 0.8:1)时,定向程度不受影响。(c)高于此临界值时,定向程度呈现时间和病毒剂量依赖性。(d)在固定病毒剂量下,P1随时间的下降符合指数规律(病毒/PMN = 5:1,特征时间为110分钟)。(e)将此特征时间作为病毒剂量的函数进行研究,结果得到一条类似于韦伯 - 费希纳定律的对数定律。这些发现表明,ECHO 9病毒仅干扰趋化反应,而不干扰化学增活反应。