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成纤维细胞运动机制:成纤维细胞前缘薄片处力与运动的定量分析

Mechanics of fibroblast locomotion: quantitative analysis of forces and motions at the leading lamellas of fibroblasts.

作者信息

Felder S, Elson E L

机构信息

Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

J Cell Biol. 1990 Dec;111(6 Pt 1):2513-26. doi: 10.1083/jcb.111.6.2513.

Abstract

Shapes, motions, and forces developed in lamellipodia and ruffles at the leading edges of primary chick embryo heart fibroblasts were characterized by differential interference contrast microscopy and digital video enhancement techniques. The initial extension of the cell edge to form a thin, planar lamellipodium parallel to the substrate surface was analyzed in two dimensions with temporal and spatial resolution of 3 s and 0.2 micron, respectively. An extension begins and ends with brief, rapid acceleration and deceleration separated by a long period of nearly constant velocity in the range of 4-7 microns/min. Extensions and retractions were initiated randomly over time. As demonstrated by optical sectioning microscopy, the extended lamellipodia formed ruffles by sharply bending upward at hinge points 2-4 microns behind their tips. Surprisingly, ruffles continued to grow in length at the same average rate after bending upward. They maintained a straight shape in vertical cross section, suggesting the ruffles were mechanically stiff. The forces required to bend ruffles of these cells and of BC3H1 cells were measured by pushing a thin quartz fishpole probe against the tip of a ruffle 7-10 microns from its base either toward or away from the center of the cell. Force was determined by measuring the bending of the probe monitored by video microscopy. Typically the probe forced the ruffle to swing rigidly in an arc about an apparent hinge at is base, and ruffles rapidly, and almost completely, recovered their shape when the probe was removed. Hence, ruffles appeared to be relatively stiff and to resist bending with forces more elastic than viscous, unlike the cell body. Ruffles on both types of cells resisted bending with forces of 15-30 mudyn/microns of displacement at their tips when pushed toward or away from the cell center. The significance of the observations for mechanisms of cell locomotion is discussed.

摘要

利用微分干涉差显微镜和数字视频增强技术,对原代鸡胚心脏成纤维细胞前缘片状伪足和皱褶中形成的形状、运动及力进行了表征。细胞边缘最初延伸形成与底物表面平行的薄而平坦的片状伪足,在二维空间中分别以3秒和0.2微米的时间和空间分辨率进行了分析。一次延伸开始和结束时分别有短暂、快速的加速和减速,中间是长达4 - 7微米/分钟的近乎恒定速度的时间段。延伸和回缩随时间随机启动。光学切片显微镜显示,延伸的片状伪足在其尖端后方2 - 4微米处的铰链点急剧向上弯曲而形成皱褶。令人惊讶的是,皱褶向上弯曲后仍以相同的平均速率继续伸长。它们在垂直截面中保持笔直形状,表明皱褶在机械上是僵硬的。通过将细石英钓竿探针从其基部7 - 10微米处推向或远离细胞中心,测量这些细胞和BC3H1细胞的皱褶弯曲所需的力。通过测量视频显微镜监测的探针弯曲来确定力。通常,探针迫使皱褶以其基部的一个明显铰链为中心刚性地弧形摆动,当探针移除时,皱褶迅速且几乎完全恢复其形状。因此,与细胞体不同,皱褶似乎相对僵硬,并且以比粘性更具弹性的力抵抗弯曲。当向细胞中心或远离细胞中心推动时,两种类型细胞上的皱褶在其尖端处以15 - 30微达因/微米的位移力抵抗弯曲。讨论了这些观察结果对细胞运动机制的意义。

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