Nested collagen matrices: A new model to study migration of human fibroblast populations in three dimensions
- Authors
- Grinnell, Frederick; Rocha, Lenaldo B; Iucu, Cristina; Rhee, Sangmyung; Jiang, Hongmei
- Issue Date
- Jan-2006
- Publisher
- Academic Press
- Keywords
- extracellular matrix; platelet-derived growth factor; lysophosphatidic acid; fibronectin; contraction; wound repair; tissue engineering
- Citation
- Experimental Cell Research, v.312, no.1, pp 86 - 94
- Pages
- 9
- Journal Title
- Experimental Cell Research
- Volume
- 312
- Number
- 1
- Start Page
- 86
- End Page
- 94
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/57714
- DOI
- 10.1016/j.yexcr.2005.10.001
- ISSN
- 0014-4827
1090-2422
- Abstract
- Fibroblast-3D collagen matrix culture provides a model system to analyze cell physiology under conditions that more closely resemble tissue than conventional 2D cell culture. Previous work has focused primarily on remodeling and contraction of collagen matrices by fibroblasts, and there has been little research on migration of cell populations within the matrix. Here, we introduce a nested collagen matrix model to analyze migration of fibroblasts in 3D collagen matrices. Nested collagen matrices were prepared by embedding contracted cell-containing matrices (also called dermal equivalents) inside cell-free matrices; migration occurred from the former to the latter. Control experiments with human dermal fragments in place of dermal equivalents confirmed the reliability of the model. Human fibroblast migration in nested collagen matrices occurred after a lag phase of 8-16 h, and cells migrating out of the inner matrices were bipolar with leading dendritic extensions. Migration was myosin 11, Rho kinase and metalloproteinase-dependent but did not require plasma fibronectin. Platelet-derived growth factor but not lysophosphatidic acid or serum stimulated cell migration, although all three of these physiological agonists promote matrix remodeling and contraction. The nested collagen matrix model is a relatively easy, rapid and quantitative method to measure migration of cell populations. Our studies using this model demonstrate important differences between regulation of fibroblast migration and remodeling in collagen matrices. (c) 2005 Elsevier Inc. All rights reserved.
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Collections - College of Natural Sciences > Department of Life Science > 1. Journal Articles
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