Diehn B
Science. 1973 Sep 14;181(4104):1009-15. doi: 10.1126/science.181.4104.1009.
The accumulation of Euglena gracilis in an illuminated region is brought about by two main mechanisms: orientation and subsequent directed movement (positive phototaxis) toward light scattered from particles in the illuminated zone; and by the trapping of cells in this region because of shock reactions experienced upon the cells encountering a sudden decrease of light intensity at the light-dark boundary (inverse photophobic responses). Phototactic orientation is mediated by inverse photophobic reactions which occur when the shadow of the stigma periodically falls upon the photoreceptor proper. Euglena also exhibits shock reactions when an already high light intensity is increased further (direct photophobic responses). The expression of both types of phobic responses depends upon stimulus intensity and adaptation of the sensory system in a seemingly complex way. A definition of the minimum components of the stimulus transduction system and a systems analytical approach to the study of input-output relationships enables one to construct an electronic analog of the cell's signal processing system that converts the photoreceptor input to commands which activate or inhibit flagellar reorientation. Computer simulation studies show that this model has considerable predictive value. It is hoped that with the approach presented in this article, a generalized model has become available for dealing with the questions of sensory transduction in aneural systems. Certainly, at this point more questions have been raised than have been answered. Where is the processing device located? Are its kinetic properties determined by electrical processes or by the rates of chemical reactions? Is the processor, and thereby the behavior of the orgamism, modulated by natural environmental parameters, and can it be modified permanently through more drastic chemical treatment of the cell? Is the system capable of permanent or transitory modification through repeated response, that is, does it exhibit phenomena analogous to learning and memory in higher organisms? These are only a few of the problems that require study in the future.
一是定向以及随后朝着光照区域中粒子散射光的定向运动(正趋光性);二是由于细胞在明暗边界处遇到光强突然降低时所经历的冲击反应(逆光性反应),细胞被捕获在该区域。趋光性定向由逆光性反应介导,当眼点的阴影周期性地落在感光体上时就会发生这种反应。当已经很高的光强进一步增加时,裸藻也会表现出冲击反应(正光性反应)。这两种类型的光性反应的表达似乎以一种复杂的方式取决于刺激强度和感觉系统的适应性。对刺激转导系统的最小组成部分进行定义并采用系统分析方法来研究输入 - 输出关系,能够构建细胞信号处理系统的电子模拟模型,该模型将感光体输入转换为激活或抑制鞭毛重新定向的指令。计算机模拟研究表明,该模型具有相当大的预测价值。希望通过本文所介绍的方法,已经有了一个通用模型可用于处理无神经系统中的感觉转导问题。当然,在这一点上,提出的问题比回答的问题更多。处理装置位于何处?其动力学特性是由电过程还是化学反应速率决定?处理器以及生物体的行为是否受到自然环境参数的调节,并且能否通过对细胞进行更剧烈的化学处理而永久改变?该系统是否能够通过重复反应进行永久或暂时的改变,也就是说,它是否表现出类似于高等生物学习和记忆的现象?这些只是未来需要研究的几个问题。