Lee J, Leonard M, Oliver T, Ishihara A, Jacobson K
Department of Cell Biology and Anatomy, University of North Carolina at Chapel Hill 27599-7090.
J Cell Biol. 1994 Dec;127(6 Pt 2):1957-64. doi: 10.1083/jcb.127.6.1957.
Traction forces produced by moving fibroblasts have been observed as distortions in flexible substrata including wrinkling of thin, silicone rubber films. Traction forces generated by fibroblast lamellae were thought to represent the forces required to move the cell forwards. However, traction forces could not be detected with faster moving cell types such as leukocytes and growth cones (Harris, A. K., D. Stopak, and P. Wild. 1981. Nature (Lond.). 290:249-251). We have developed a new assay in which traction forces produced by rapidly locomoting fish keratocytes can be detected by the two-dimensional displacements of small beads embedded in the plane of an elastic substratum. Traction forces were not detected at the rapidly extending front edge of the cell. Instead the largest traction forces were exerted perpendicular to the left and right cell margins. The maximum traction forces exerted by keratocytes were estimated to be approximately 2 x 10(-8) N. The pattern of traction forces can be related to the locomotion of a single keratocyte in terms of lamellar contractility and area of close cell-substratum contact.
移动的成纤维细胞产生的牵引力已被观察到会使柔性基质产生变形,包括薄硅橡胶膜的起皱。成纤维细胞薄片产生的牵引力被认为代表了细胞向前移动所需的力。然而,对于白细胞和生长锥等移动速度更快的细胞类型,无法检测到牵引力(哈里斯,A.K.,D.斯托帕克,和P.怀尔德。1981年。《自然》(伦敦)。290:249 - 251)。我们开发了一种新的检测方法,通过嵌入弹性基质平面内的小珠子的二维位移,可以检测快速移动的鱼角膜细胞产生的牵引力。在细胞快速延伸的前沿未检测到牵引力。相反,最大的牵引力垂直于细胞的左右边缘施加。角膜细胞施加的最大牵引力估计约为2×10⁻⁸牛。根据片状收缩性和紧密的细胞 - 基质接触面积,牵引力模式可以与单个角膜细胞的运动相关联。