Harris A K, Stopak D, Wild P
Nature. 1981 Mar 19;290(5803):249-51. doi: 10.1038/290249a0.
To make visible the traction forces exerted by individuals cells, we have previously developed a method of culturing them on thin distortable sheets of silicone rubber. We have now used this method to compare the forces exerted by various differentiated cell types and have examined the effects of cellular traction on re-precipitated collagen-matrices. We find that the strength of cellular traction differs greatly between cell types and this traction is paradoxically weakest in the most mobile and invasive cells (leukocytes and nerve growth cones). Untransformed fibroblasts exert forces very much larger than those actually needed for locomotion. This strong traction distorts collagen gels dramatically, creating patterns similar to tendons and organ capsules. We propose that this morphogenetic rearrangement of extracellular matrices is the primary function of fibroblast traction and explains its excessive strength.
为了使单个细胞施加的牵引力可见,我们之前开发了一种在可变形的薄硅橡胶片上培养细胞的方法。我们现在使用这种方法来比较各种分化细胞类型施加的力,并研究细胞牵引力对再沉淀胶原基质的影响。我们发现,细胞牵引力的强度在不同细胞类型之间差异很大,而且矛盾的是,在最具移动性和侵袭性的细胞(白细胞和神经生长锥)中,这种牵引力最弱。未转化的成纤维细胞施加的力比实际运动所需的力大得多。这种强大的牵引力会使胶原凝胶显著变形,形成类似于肌腱和器官包膜的图案。我们认为,细胞外基质的这种形态发生重排是成纤维细胞牵引力的主要功能,并解释了其过度的强度。