Oliver T, Dembo M, Jacobson K
Department of Cell Biology and Anatomy, University of North Carolina at Chapel Hill, Durham 27599-7090, USA.
Cell Motil Cytoskeleton. 1995;31(3):225-40. doi: 10.1002/cm.970310306.
A means of determining quantitative maps of the tractions exerted by locomoting cells on a substratum has been developed. This method is similar to the Harris silicone substratum assay [Harris et al., 1980: Science 208:177-179], but uses an improved non-wrinkling film that deforms more predictably in response to traction forces. The method also utilizes a mathematical analysis of rubber deformation to produce the final map of the distribution of tractions. The resulting maps consistently showed that fish keratocytes exert a steady-state "pinching" on the substratum, perpendicular to the cell's direction of locomotion. No significant rearward tractions were detected at or near the front edge of the cell. Likewise, no significant forward tractions associated with peeling of adhesions were found at the back of the cell. A second assay uses deflection of a lightly attached glass microneedle to measure the total force exerted by locomoting cells. Forces of approximately 4.5 x 10(-3) dyn were required to "stall" locomoting keratocytes. The implications of these findings for cell movement are discussed.
一种确定运动细胞对基质施加的牵引力定量图谱的方法已经开发出来。这种方法类似于哈里斯硅酮基质测定法[哈里斯等人,1980年:《科学》208:177 - 179],但使用了一种改进的无皱纹薄膜,其在牵引力作用下的变形更可预测。该方法还利用橡胶变形的数学分析来生成牵引力分布的最终图谱。所得图谱一致显示,鱼角膜细胞在基质上施加垂直于细胞运动方向的稳态“挤压”。在细胞前缘或其附近未检测到明显的向后牵引力。同样,在细胞后部也未发现与粘连剥离相关的明显向前牵引力。第二种测定法使用轻轻附着的玻璃微针的偏转来测量运动细胞施加的总力。使运动的角膜细胞“停止”需要约4.5×10⁻³达因的力。讨论了这些发现对细胞运动的意义。