The effect5 of sulfated polysaccharides on the growth and chemotdxis of endothel i d cells promoted by basic fibroblast growth factor (brGF), a heparin-binding growth factor, and epidermal growth factor (EGF), a non-heparin-binding growth factor, were examined. The binding abilities of these two gro
Differential effects of matrix and growth factors on endothelial and fibroblast motility: Application of a modified cell migration assay
✍ Scribed by Remco van Horssen; Niels Galjart; Joost A.P. Rens; Alexander M.M. Eggermont; Timo L.M. ten Hagen
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 836 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Cell migration is crucial in virtually every biological process and strongly depends on the nature of the surrounding matrix. An assay that enables real‐time studies on the effects of defined matrix components and growth factors on cell migration is not available. We have set up a novel, quantitative migration assay, which enables unharmed cells to migrate along a defined matrix. Here, we used this so‐called barrier‐assay to define the contribution of fibronectin (FN) and Collagen‐I (Col‐I) to vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and lysophosphatidic acid (LPA)‐induced cell migration of endothelial cells (EC) and fibroblasts. In EC, both FN and Col‐I stimulated migration, but FN‐induced motility was random, while net movement was inhibited. Addition of bFGF and VEGF overcame the effect of FN, with VEGF causing directional movement. In contrast, in 3T3 fibroblasts, FN stimulated motility and this effect was enhanced by bFGF. This motility was more efficient and morphologically completely different compared to LPA stimulation. Strikingly, directional migration of EC was not paralleled by higher amounts of stable microtubules (MT) or an increased reorientation of the microtubule‐organizing centre (MTOC). For EC, the FN effect appeared concentration dependent; high FN was able to induce migration, while for fibroblasts both low and high concentrations of FN induced motility. Besides showing distinct responses of the different cells to the same factors, these results address contradictive reports on FN and show that the interplay between matrix components and growth factors determines both pattern and regulation of cell migration. J. Cell. Biochem. 99: 1536–1552, 2006. © 2006 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
Recent studies in several neuronal lineages suggest that extrinsic factors such as polypeptide growth factors regulate various stages of neuronal development, from initial commitment of multipotent progenitors to induction of specific gene expression that is characteristic of terminal neuronal diffe
It has been suggested that gangliosides can influence the growth of cells by modulation of growth-factor-receptor signalling. The activation of endothelial cells (EC) during angiogenesis is crucial for tumour growth and for metastasis, also for numerous other physiological and pathological situation
## Abstract The role of the matricellular protein SPARC (secreted protein, acidic and rich in cysteine) in modulation of vascular cell proliferation is believed to be mediated, in part, by its ability to regulate the activity of certain growth factors through direct binding. In this study, we demon
The pigeon crop-sac is an underappreciated and underutilized model that can be used to study the direct and indirect effects of hormones, growth factors, and other agents on cell proliferation and differentiative processes in vivo. It can thus allow the uncertainties that attend many in vitro method