Oliver T, Dembo M, Jacobson K
Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina 27708-0300, USA.
J Cell Biol. 1999 May 3;145(3):589-604. doi: 10.1083/jcb.145.3.589.
Strong, actomyosin-dependent, pinching tractions in steadily locomoting (gliding) fish keratocytes revealed by traction imaging present a paradox, since only forces perpendicular to the direction of locomotion are apparent, leaving the actual propulsive forces unresolved. When keratocytes become transiently "stuck" by their trailing edge and adopt a fibroblast-like morphology, the tractions opposing locomotion are concentrated into the tail, leaving the active pinching and propulsive tractions clearly visible under the cell body. Stuck keratocytes can develop approximately 1 mdyn (10,000 pN) total propulsive thrust, originating in the wings of the cell. The leading lamella develops no detectable propulsive traction, even when the cell pulls on its transient tail anchorage. The separation of propulsive and adhesive tractions in the stuck phenotype leads to a mechanically consistent hypothesis that resolves the traction paradox for gliding keratocytes: the propulsive tractions driving locomotion are normally canceled by adhesive tractions resisting locomotion, leaving only the pinching tractions as a resultant. The resolution of the traction pattern into its components specifies conditions to be met for models of cytoskeletal force production, such as the dynamic network contraction model (Svitkina, T.M., A.B. Verkhovsky, K.M. McQuade, and G.G. Borisy. 1997. J. Cell Biol. 139:397-415). The traction pattern associated with cells undergoing sharp turns differs markedly from the normal pinching traction pattern, and can be accounted for by postulating an asymmetry in contractile activity of the opposed lateral wings of the cell.
通过牵引力成像显示,在持续移动(滑行)的鱼类角膜细胞中,强大的、依赖于肌动球蛋白的收缩牵引力呈现出一个悖论,因为只有垂直于移动方向的力是明显的,而实际的推进力仍未得到解释。当角膜细胞的后缘暂时“卡住”并呈现成纤维细胞样形态时,与移动相反的牵引力集中在尾部,使得活跃的收缩和推进牵引力在细胞体下方清晰可见。卡住的角膜细胞可产生约1达因(10,000皮牛)的总推进力,该力起源于细胞的侧翼。即使细胞拉动其暂时的尾部固定点,前缘薄片也不会产生可检测到的推进牵引力。在卡住的表型中推进力和黏附力的分离导致了一个机械上一致的假设,该假设解决了滑行角膜细胞的牵引力悖论:驱动移动的推进力通常被抵抗移动的黏附力抵消,只留下收缩牵引力作为合力。将牵引力模式分解为其组成部分,为细胞骨架力产生模型(如动态网络收缩模型,Svitkina, T.M., A.B. Verkhovsky, K.M. McQuade, and G.G. Borisy. 1997. J. Cell Biol. 139:397 - 415)规定了需要满足的条件。与急转弯的细胞相关的牵引力模式与正常的收缩牵引力模式明显不同,可以通过假设细胞相对侧翼的收缩活动不对称来解释。