Individual versus Collective Fibroblast Spreading and Migration: Regulation by Matrix Composition in 3-D Culture
| Autor: | Peter Ririe, Lisha Ma, W. Matthew Petroll, Miguel Miron-Mendoza, Xihui Lin |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2012 |
| Předmět: |
Corneal Keratocytes
Time-Lapse Imaging Fibrin Article Fibroblast migration Extracellular matrix Cellular and Molecular Neuroscience Imaging Three-Dimensional Cell Movement medicine Humans Fluorescent Antibody Technique Indirect Fibroblast Cells Cultured Cell Proliferation Skin Microscopy Confocal biology Cadherin Chemistry Cell migration Fibroblasts Cadherins Sensory Systems Fibronectins Cell biology Extracellular Matrix Fibronectin Ophthalmology medicine.anatomical_structure biology.protein Collagen Wound healing |
| Popis: | Extracellular matrix (ECM) supplies both physical and chemical signals to cells and provides a substrate through which fibroblasts migrate during wound repair. To directly assess how ECM composition regulates this process, we used a nested 3D matrix model in which cell-populated collagen buttons were embedded in cell-free collagen or fibrin matrices. Time-lapse microscopy was used to record the dynamic pattern of cell migration into the outer matrices, and 3-D confocal imaging was used to assess cell connectivity and cytoskeletal organization. Corneal fibroblasts stimulated with PDGF migrated more rapidly into collagen as compared to fibrin. In addition, the pattern of fibroblast migration into fibrin and collagen ECMs was strikingly different. Corneal fibroblasts migrating into collagen matrices developed dendritic processes and moved independently, whereas cells migrating into fibrin matrices had a more fusiform morphology and formed an interconnected meshwork. A similar pattern was observed when using dermal fibroblasts, suggesting that this response in not unique to corneal cells. We next cultured corneal fibroblasts within and on top of standard collagen and fibrin matrices to assess the impact of ECM composition on the cell spreading response. Similar differences in cell morphology and connectivity were observed – cells remained separated on collagen but coalesced into clusters on fibrin. Cadherin was localized to junctions between interconnected cells, whereas fibronectin was present both between cells and at the tips of extending cell processes. Cells on fibrin matrices also developed more prominent stress fibers than those on collagen matrices. Importantly, these spreading and migration patterns were consistently observed on both rigid and compliant substrates, thus differences in ECM mechanical stiffness were not the underlying cause. Overall, these results demonstrate for the first time that ECM protein composition alone (collagen vs. fibrin) can induce a switch from individual to collective fibroblast spreading and migration in 3-D culture. Similar processes may also influence cell behavior during wound healing, development, tumor invasion and repopulation of engineered tissues. |
| Databáze: | OpenAIRE |
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