CURTIS A S
J Cell Biol. 1964 Feb;20(2):199-215. doi: 10.1083/jcb.20.2.199.
An optical technique for measuring the thickness of thin films has been adapted and evaluated for studying the structure of the adhesion of cells to glass in tissue culture. This technique, which is termed interference reflection microscopy, has been used to study embryonic chick heart fibroblasts. These findings have been observed: in normal culture medium the closest approach of the cell surface to substrate in its adhesions is ca. 100 A, much of the cell surface lying farther away; chemical treatments which bring the cell surface to near its charge reversal point reduce the closest approach of adhesions to <50 A, probably to <30 A; chemical treatments which increase surface charge increase the nearest approach of cell and substrate in adhesions from ca. 100 A; high osmotic concentration of a non-polar substance, i.e. sucrose, does not affect the distance between cell and substrate in the adhesions. In addition, optical evidence indicates that there is no extracellular material between cell and glass in the adhesions. When cells de-adhere from glass, they appear not to leave fragments behind. The adhesive sites in these fibroblasts appear to be confined to the edge of the side of the cell facing the substrate and to the pseudopods. The significance of this is discussed in relation to the phenomenon of contact inhibition. Evidence is presented that the mechanism of cell adhesion does not involve calcium atoms binding cells to substrate by combining with carboxyl groups on cell surface, substrate, and with a cement substance. Osmium tetroxide fixation results in a final separation of 100 to 200 A between cell and substrate: there are reasons for thinking that this fairly close approach to the condition in life is produced as an artefact. The results can be accounted for only in terms of the action of electrostatic repulsive forces and an attractive force, probably the van der Waals-London forces. Biological arguments suggest that these results are equally applicable for cell-to-cell adhesions.
一种用于测量薄膜厚度的光学技术已被改编并评估,用于研究组织培养中细胞与玻璃的粘附结构。这种技术被称为干涉反射显微镜,已用于研究鸡胚心脏成纤维细胞。观察到以下结果:在正常培养基中,细胞表面在粘附时与底物的最接近距离约为100埃,大部分细胞表面距离更远;使细胞表面接近其电荷反转点的化学处理将粘附的最接近距离减小到<50埃,可能<30埃;增加表面电荷的化学处理使细胞与底物在粘附中的最近距离从约100埃增加;非极性物质(即蔗糖)的高渗透压浓度不影响细胞与底物在粘附中的距离。此外,光学证据表明,在粘附中细胞与玻璃之间没有细胞外物质。当细胞从玻璃上脱粘时,它们似乎不会留下碎片。这些成纤维细胞中的粘附位点似乎局限于细胞面向底物一侧的边缘和伪足。这与接触抑制现象相关的意义进行了讨论。有证据表明,细胞粘附机制不涉及钙原子通过与细胞表面、底物上的羧基以及一种胶结物质结合将细胞与底物结合。四氧化锇固定导致细胞与底物之间最终分离100至200埃:有理由认为这种与生命状态相当接近的情况是作为一种假象产生的。结果只能用静电排斥力和一种吸引力(可能是范德华 - 伦敦力)的作用来解释。生物学观点表明,这些结果同样适用于细胞间粘附。