Jones G E, Gillett R, Partridge T
J Cell Sci. 1976 Oct;22(1):21-33. doi: 10.1242/jcs.22.1.21.
Haemocytes suspended in the blood of the limpet Patella vulgata rapidly form microspikes and aggregate in response to withdrawal from the haemocoel. It has previously been suggested that the contacts between colliding cells in shaken suspension are stabilized by the rapid spreading of participant cells over each other's surfaces by a microspike-dependent process. In this communication we report that an electron-microscopic study of the contacts formed between cells in the early stages of aggregation suggests that intercellular contact elicits a rapid response from the organelles concerned with cell motility. This response leads to the rapid progression of each initial collision through 3 major categories of contact morphology, namely cell body/lamella, lamella/lamella and cell body/cell body. There is a concomitant increase in the area of mutually contacting surface between participating cells. On the basis of these results, a model is constructed for the participation of sub-surface components in the process of cellular aggregation. The sequence of development of contact found between aggregating cells is envisaged to be a consequence of cellular locomotory activities resembling those by which these cells spread on to a solid substrate. Included in this process is an element of intercellular recognition. It is suggested that the involvement of motile elements in cell aggregation is a general feature of aggregating cells. This would permit a re-interpretation of aggregation experiments which show specificity of cell adhesion, for total adhesive interactions between cells would depend not only on the adhesiveness per unit area of contacting cell surface but also on the extent or rate of formation of flat contact areas. The latter element could be regulated by a recognition system between contacting cells independently of the force per unit area which holds the 2 surfaces together.
悬浮在帽贝(Patella vulgata)血液中的血细胞会迅速形成微刺,并在从血腔中取出后聚集。此前有研究表明,在摇晃悬浮液中相互碰撞的细胞之间的接触,是通过参与细胞通过依赖微刺的过程在彼此表面快速铺展而得以稳定的。在本通讯中,我们报告了一项电子显微镜研究结果,该研究对聚集早期阶段细胞之间形成的接触进行了观察,结果表明细胞间接触会引发与细胞运动相关的细胞器的快速反应。这种反应导致每次初始碰撞迅速经历3种主要的接触形态类别,即细胞体/薄片、薄片/薄片和细胞体/细胞体。参与细胞之间相互接触表面的面积也随之增加。基于这些结果,构建了一个关于细胞表面下成分参与细胞聚集过程的模型。聚集细胞之间发现的接触发展顺序被设想为细胞运动活动的结果,类似于这些细胞在固体基质上铺展的活动。这个过程包括细胞间识别的因素。有人提出,运动元件参与细胞聚集是聚集细胞的一个普遍特征。这将允许对显示细胞粘附特异性的聚集实验进行重新解释,因为细胞之间的总粘附相互作用不仅取决于接触细胞表面每单位面积的粘附性,还取决于平坦接触面积的形成程度或速率。后一个因素可以由接触细胞之间的识别系统独立于将两个表面结合在一起的每单位面积的力来调节。