Galbraith C G, Sheetz M P
Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9114-8. doi: 10.1073/pnas.94.17.9114.
We have measured the traction forces generated by fibroblasts using a novel micromachined device that is capable of determining the subcellular forces generated by individual adhesive contacts. The front of migrating fibroblasts produced intermittent rearward forces whereas the tail produced larger forward directed forces. None of the forces were steady; they all had periodic fluctuations. The transition between forward and rearward traction forces occurred at the nucleus, not at the rear of the cell or the border between the endoplasm and the ectoplasm. We propose that the coupling of lamella extensions to fluctuating rearward tractions in front of the nuclear region move the front of a fibroblast forward, while force-facilitated release of rear adhesive contacts and anterior-directed tractions allow the region behind the nucleus to advance.
我们使用一种新型微机械装置测量了成纤维细胞产生的牵引力,该装置能够确定单个黏附接触产生的亚细胞力。迁移的成纤维细胞前端产生间歇性向后的力,而尾部产生更大的向前的力。这些力都不稳定;它们都有周期性波动。向前和向后牵引力之间的转变发生在细胞核处,而不是细胞尾部或内质与外质之间的边界处。我们提出,在核区域前方,薄片延伸与波动的向后牵引力的耦合推动成纤维细胞前端向前移动,而力促进后方黏附接触的释放和向前的牵引力则使细胞核后方的区域前进。